diff --git a/.github/workflows/build.yml b/.github/workflows/build.yml
index 1d1cbf6f8..0005abfa8 100644
--- a/.github/workflows/build.yml
+++ b/.github/workflows/build.yml
@@ -40,12 +40,18 @@ jobs:
# Only generate the distribution if this is the default branch
GENERATE_DIST: ${{ env.DEFAULT_BRANCH == github.ref_name && '1' || '0' }}
- - name: Publish Release
+ - name: Publish Latest Release
+ id: publish-release
if: ${{ env.DEFAULT_BRANCH == github.ref_name && github.event_name == 'push' && github.base_ref == '' }}
- uses: "marvinpinto/action-automatic-releases@latest"
- with:
- repo_token: "${{ secrets.PAT }}"
- automatic_release_tag: "latest"
- prerelease: true
- title: "Development Build: ${{ env.DEFAULT_BRANCH }}"
- files: /home/runner/work/_temp/_github_home/lkDist/discvr/DISCVR-*
\ No newline at end of file
+ env:
+ GH_TOKEN: "${{ secrets.PAT }}"
+ run: |
+ LK_VERSION=$(cat /home/runner/work/_temp/_github_home/lkDist/release.txt | sed 's/-SNAPSHOT//g')
+ cd /home/runner/work/_temp/_github_home/labkey_build/${LK_VERSION}/server/server/modules/DiscvrLabKeyModules
+ COUNT=$(gh release list | grep 'latest' | wc -l)
+ if [ $COUNT != '0' ];then gh release delete 'latest' --cleanup-tag -y; fi
+
+ git push -f origin "latest"
+
+ gh release create 'latest' --verify-tag --generate-notes --prerelease --title "Development Build: ${{ env.DEFAULT_BRANCH }}"
+ gh release upload 'latest' /home/runner/work/_temp/_github_home/lkDist/discvr/DISCVR-*
\ No newline at end of file
diff --git a/.github/workflows/build_latest.yml b/.github/workflows/build_latest.yml
index dfe4bc088..f194da930 100644
--- a/.github/workflows/build_latest.yml
+++ b/.github/workflows/build_latest.yml
@@ -36,13 +36,18 @@ jobs:
env:
GENERATE_DIST: 1
- # See: https://github.com/marketplace/actions/automatic-releases
- - name: Deploy Build
- if: ${{ env.DEFAULT_BRANCH == github.ref_name }}
- uses: "marvinpinto/action-automatic-releases@latest"
- with:
- repo_token: "${{ secrets.PAT }}"
- automatic_release_tag: "latest"
- prerelease: true
- title: "Development Build: ${{ fromJson(steps.get_default_branch.outputs.data).default_branch }}"
- files: /home/runner/work/_temp/_github_home/lkDist/discvr/DISCVR-*
\ No newline at end of file
+ - name: Publish Latest Release
+ id: publish-release
+ if: ${{ env.DEFAULT_BRANCH == github.ref_name && github.event_name == 'push' && github.base_ref == '' }}
+ env:
+ GH_TOKEN: "${{ secrets.PAT }}"
+ run: |
+ LK_VERSION=$(cat /home/runner/work/_temp/_github_home/lkDist/release.txt | sed 's/-SNAPSHOT//g')
+ cd /home/runner/work/_temp/_github_home/labkey_build/${LK_VERSION}/server/server/modules/DiscvrLabKeyModules
+ COUNT=$(gh release list | grep 'latest' | wc -l)
+ if [ $COUNT != '0' ];then gh release delete 'latest' --cleanup-tag -y; fi
+
+ git push -f origin "latest"
+
+ gh release create 'latest' --verify-tag --generate-notes --prerelease --title "Development Build: ${{ env.DEFAULT_BRANCH }}"
+ gh release upload 'latest' /home/runner/work/_temp/_github_home/lkDist/discvr/DISCVR-*
\ No newline at end of file
diff --git a/QueryExtensions/build.gradle b/QueryExtensions/build.gradle
new file mode 100644
index 000000000..8a83d15d3
--- /dev/null
+++ b/QueryExtensions/build.gradle
@@ -0,0 +1,9 @@
+import org.labkey.gradle.util.BuildUtils
+
+plugins {
+ id 'org.labkey.build.module'
+}
+
+dependencies {
+ BuildUtils.addLabKeyDependency(project: project, config: "modules", depProjectPath: ":server:modules:DiscvrLabKeyModules:discvrcore", depProjectConfig: "published", depExtension: "module")
+}
diff --git a/QueryExtensions/module.properties b/QueryExtensions/module.properties
new file mode 100644
index 000000000..3044be8be
--- /dev/null
+++ b/QueryExtensions/module.properties
@@ -0,0 +1,5 @@
+ModuleClass: org.labkey.queryextensions.QueryExtensionsModule
+Label: Query Extensions
+Description: This module contains low-level extensions to the LabKey Query layer
+License: Apache 2.0
+LicenseURL: http://www.apache.org/licenses/LICENSE-2.0
diff --git a/QueryExtensions/resources/schemas/dbscripts/postgresql/queryextensions-0.00-23.000.sql b/QueryExtensions/resources/schemas/dbscripts/postgresql/queryextensions-0.00-23.000.sql
new file mode 100644
index 000000000..c9855ba77
--- /dev/null
+++ b/QueryExtensions/resources/schemas/dbscripts/postgresql/queryextensions-0.00-23.000.sql
@@ -0,0 +1,19 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+-- Create schema, tables, indexes, and constraints used for QueryExtensions module here
+-- All SQL VIEW definitions should be created in queryextensions-create.sql and dropped in queryextensions-drop.sql
+CREATE SCHEMA queryextensions;
diff --git a/QueryExtensions/resources/schemas/dbscripts/sqlserver/queryextensions-0.00-23.000.sql b/QueryExtensions/resources/schemas/dbscripts/sqlserver/queryextensions-0.00-23.000.sql
new file mode 100644
index 000000000..d12b98db4
--- /dev/null
+++ b/QueryExtensions/resources/schemas/dbscripts/sqlserver/queryextensions-0.00-23.000.sql
@@ -0,0 +1,20 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+-- Create schema, tables, indexes, and constraints used for QueryExtensions module here
+-- All SQL VIEW definitions should be created in queryextensions-create.sql and dropped in queryextensions-drop.sql
+CREATE SCHEMA queryextensions;
+GO
\ No newline at end of file
diff --git a/QueryExtensions/resources/schemas/queryextensions.xml b/QueryExtensions/resources/schemas/queryextensions.xml
new file mode 100644
index 000000000..867c4794c
--- /dev/null
+++ b/QueryExtensions/resources/schemas/queryextensions.xml
@@ -0,0 +1,20 @@
+
+
+
\ No newline at end of file
diff --git a/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsController.java b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsController.java
new file mode 100644
index 000000000..95772162d
--- /dev/null
+++ b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsController.java
@@ -0,0 +1,37 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+package org.labkey.queryextensions;
+
+import org.labkey.api.action.SimpleViewAction;
+import org.labkey.api.action.SpringActionController;
+import org.labkey.api.security.RequiresPermission;
+import org.labkey.api.security.permissions.ReadPermission;
+import org.labkey.api.view.JspView;
+import org.labkey.api.view.NavTree;
+import org.springframework.validation.BindException;
+import org.springframework.web.servlet.ModelAndView;
+
+public class QueryExtensionsController extends SpringActionController
+{
+ private static final DefaultActionResolver _actionResolver = new DefaultActionResolver(QueryExtensionsController.class);
+ public static final String NAME = "queryextensions";
+
+ public QueryExtensionsController()
+ {
+ setActionResolver(_actionResolver);
+ }
+}
diff --git a/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsManager.java b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsManager.java
new file mode 100644
index 000000000..62994f0b3
--- /dev/null
+++ b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsManager.java
@@ -0,0 +1,32 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+package org.labkey.queryextensions;
+
+public class QueryExtensionsManager
+{
+ private static final QueryExtensionsManager _instance = new QueryExtensionsManager();
+
+ private QueryExtensionsManager()
+ {
+
+ }
+
+ public static QueryExtensionsManager get()
+ {
+ return _instance;
+ }
+}
\ No newline at end of file
diff --git a/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsModule.java b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsModule.java
new file mode 100644
index 000000000..d383227e4
--- /dev/null
+++ b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsModule.java
@@ -0,0 +1,84 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+package org.labkey.queryextensions;
+
+import org.jetbrains.annotations.NotNull;
+import org.jetbrains.annotations.Nullable;
+import org.labkey.api.data.Container;
+import org.labkey.api.module.DefaultModule;
+import org.labkey.api.module.ModuleContext;
+import org.labkey.api.view.WebPartFactory;
+
+import java.util.Collection;
+import java.util.Collections;
+import java.util.Set;
+
+public class QueryExtensionsModule extends DefaultModule
+{
+ public static final String NAME = "QueryExtensions";
+
+ @Override
+ public String getName()
+ {
+ return NAME;
+ }
+
+ @Override
+ public @Nullable Double getSchemaVersion()
+ {
+ return 23.000;
+ }
+
+ @Override
+ public boolean hasScripts()
+ {
+ return true;
+ }
+
+ @Override
+ @NotNull
+ protected Collection createWebPartFactories()
+ {
+ return Collections.emptyList();
+ }
+
+ @Override
+ protected void init()
+ {
+ addController(QueryExtensionsController.NAME, QueryExtensionsController.class);
+ }
+
+ @Override
+ public void doStartup(ModuleContext moduleContext)
+ {
+
+ }
+
+ @Override
+ @NotNull
+ public Collection getSummary(Container c)
+ {
+ return Collections.emptyList();
+ }
+
+ @Override
+ @NotNull
+ public Set getSchemaNames()
+ {
+ return Collections.singleton(QueryExtensionsSchema.NAME);
+ }
+}
\ No newline at end of file
diff --git a/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsSchema.java b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsSchema.java
new file mode 100644
index 000000000..e5bcabc15
--- /dev/null
+++ b/QueryExtensions/src/org/labkey/queryextensions/QueryExtensionsSchema.java
@@ -0,0 +1,49 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+package org.labkey.queryextensions;
+
+import org.labkey.api.data.DbSchema;
+import org.labkey.api.data.DbSchemaType;
+import org.labkey.api.data.dialect.SqlDialect;
+
+public class QueryExtensionsSchema
+{
+ private static final QueryExtensionsSchema _instance = new QueryExtensionsSchema();
+ public static final String NAME = "queryextensions";
+
+ public static QueryExtensionsSchema getInstance()
+ {
+ return _instance;
+ }
+
+ private QueryExtensionsSchema()
+ {
+ // private constructor to prevent instantiation from
+ // outside this class: this singleton should only be
+ // accessed via org.labkey.queryextensions.QueryExtensionsSchema.getInstance()
+ }
+
+ public DbSchema getSchema()
+ {
+ return DbSchema.get(NAME, DbSchemaType.Module);
+ }
+
+ public SqlDialect getSqlDialect()
+ {
+ return getSchema().getSqlDialect();
+ }
+}
diff --git a/QueryExtensions/test/src/org/labkey/test/tests/queryextensions/QueryExtensionsTest.java b/QueryExtensions/test/src/org/labkey/test/tests/queryextensions/QueryExtensionsTest.java
new file mode 100644
index 000000000..9065c8158
--- /dev/null
+++ b/QueryExtensions/test/src/org/labkey/test/tests/queryextensions/QueryExtensionsTest.java
@@ -0,0 +1,82 @@
+/*
+ * Copyright (c) 2023 LabKey Corporation
+ *
+ * Licensed under the Apache License, Version 2.0 (the "License");
+ * you may not use this file except in compliance with the License.
+ * You may obtain a copy of the License at
+ *
+ * http://www.apache.org/licenses/LICENSE-2.0
+ *
+ * Unless required by applicable law or agreed to in writing, software
+ * distributed under the License is distributed on an "AS IS" BASIS,
+ * WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
+ * See the License for the specific language governing permissions and
+ * limitations under the License.
+ */
+
+package org.labkey.test.tests.queryextensions;
+
+import org.junit.Before;
+import org.junit.BeforeClass;
+import org.junit.Test;
+import org.junit.experimental.categories.Category;
+import org.labkey.test.BaseWebDriverTest;
+import org.labkey.test.TestTimeoutException;
+import org.labkey.test.categories.InDevelopment;
+
+import java.util.Collections;
+import java.util.List;
+
+@Category({InDevelopment.class})
+public class QueryExtensionsTest extends BaseWebDriverTest
+{
+ @Override
+ protected void doCleanup(boolean afterTest) throws TestTimeoutException
+ {
+ _containerHelper.deleteProject(getProjectName(), afterTest);
+ }
+
+ @BeforeClass
+ public static void setupProject()
+ {
+ QueryExtensionsTest init = (QueryExtensionsTest)getCurrentTest();
+
+ init.doSetup();
+ }
+
+ private void doSetup()
+ {
+ _containerHelper.createProject(getProjectName(), null);
+ }
+
+ @Before
+ public void preTest()
+ {
+ goToProjectHome();
+ }
+
+ @Test
+ public void testQueryExtensionsModule()
+ {
+ _containerHelper.enableModule("QueryExtensions");
+
+ }
+
+ @Override
+ protected BrowserType bestBrowser()
+ {
+ return BrowserType.CHROME;
+ }
+
+ @Override
+ protected String getProjectName()
+ {
+ return "QueryExtensionsTest Project";
+ }
+
+ @Override
+ public List getAssociatedModules()
+ {
+ return Collections.singletonList("QueryExtensions");
+ }
+}
\ No newline at end of file
diff --git a/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/HasJobParams.java b/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/HasJobParams.java
index 3551e51a1..210230f17 100644
--- a/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/HasJobParams.java
+++ b/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/HasJobParams.java
@@ -2,6 +2,7 @@
import org.json.JSONObject;
+import java.io.File;
import java.util.Map;
/**
@@ -12,4 +13,6 @@ public interface HasJobParams
Map getJobParams();
JSONObject getParameterJson();
+
+ File getParametersFile();
}
diff --git a/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/SequencePipelineService.java b/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/SequencePipelineService.java
index f9d1ddf10..a5ad1e5e7 100644
--- a/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/SequencePipelineService.java
+++ b/SequenceAnalysis/api-src/org/labkey/api/sequenceanalysis/pipeline/SequencePipelineService.java
@@ -144,4 +144,6 @@ static public void setInstance(SequencePipelineService instance)
// Note: this primarily exists for testing. The returned TaskFileManager does not have key values set: SequenceJob, WorkingDir (File) and WorkDirectory
abstract public TaskFileManager getTaskFileManager();
+
+ abstract public Set getResourceSettings();
}
diff --git a/SequenceAnalysis/build.gradle b/SequenceAnalysis/build.gradle
index c2e887a19..a0cda32aa 100644
--- a/SequenceAnalysis/build.gradle
+++ b/SequenceAnalysis/build.gradle
@@ -10,13 +10,9 @@ import java.util.regex.Matcher
repositories {
mavenCentral()
- // Added for org.clojars.chapmanb:sam dependency required by com.github.samtools:htsjdk
+ // Added for jhdf5 from FASTQC / sequence analysis module
maven {
- url "https://clojars.org/repo"
- }
- // Added for org.clojars.chapmanb:sam
- maven {
- url "https://maven.scijava.org/content/groups/public"
+ url "https://maven.scijava.org/content/groups/public/"
}
}
@@ -99,13 +95,26 @@ dependencies {
BuildUtils.addExternalDependency(
project,
new ExternalDependency(
- 'org.clojars.chapmanb:sam:1.96',
- 'picard tools',
- 'picard tools',
- 'http://sourceforge.net/projects/picard/',
+ 'cisd:jhdf5:19.04.1',
+ 'JHDF5',
+ 'JHDF5',
+ 'https://unlimited.ethz.ch/display/JHDF/',
+ ExternalDependency.BSD_LICENSE_NAME,
+ ExternalDependency.BSD_LICENSE_URL,
+ 'JHDF5 is a Java binding for HDF5. Used by FastQC'
+ )
+ )
+
+ BuildUtils.addExternalDependency(
+ project,
+ new ExternalDependency(
+ 'net.iharder:base64:2.3.8',
+ 'Base64',
+ 'Base64',
+ 'http://iharder.net/base64/',
ExternalDependency.MIT_LICENSE_NAME,
ExternalDependency.MIT_LICENSE_URL,
- 'Library for working with SAM/BAM files. Used by FastQC'
+ 'Library for Base64 encoding. Used by FastQC'
)
)
implementation "net.sf.opencsv:opencsv:${opencsvVersion}"
@@ -156,6 +165,7 @@ dependencies {
apiImplementation "org.apache.commons:commons-math3:${commonsMath3Version}"
BuildUtils.addLabKeyDependency(project: project, config: "modules", depProjectPath: ":server:modules:LabDevKitModules:laboratory", depProjectConfig: "published", depExtension: "module")
BuildUtils.addLabKeyDependency(project: project, config: "modules", depProjectPath: ":server:modules:LabDevKitModules:LDK", depProjectConfig: "published", depExtension: "module")
+ BuildUtils.addLabKeyDependency(project: project, config: "modules", depProjectPath: ":server:modules:DiscvrLabKeyModules:discvrcore", depProjectConfig: "published", depExtension: "module")
}
diff --git a/SequenceAnalysis/resources/external/basicHistogram.r b/SequenceAnalysis/resources/external/basicHistogram.r
deleted file mode 100644
index 7e9e1fc10..000000000
--- a/SequenceAnalysis/resources/external/basicHistogram.r
+++ /dev/null
@@ -1,62 +0,0 @@
-options(warn = -1)
-
-library(reshape)
-library(lattice)
-library(plyr)
-library(ggplot2)
-library(grid)
-library(perm)
-library(gridExtra)
-library(naturalsort)
-
-library(getopt);
-library(Matrix);
-
-options(scipen=1000000000)
-
-spec <- matrix(c(
- 'inputFile', 'i', 1, "character",
- 'outputFile', 'o', 1, "character",
- 'plotTitle', 't', 2, "character",
- 'xLabel', NA, 2, "character",
- 'colIdx', 'c', 1, "integer",
- 'binWidth', NA, 2, "integer",
- 'maxValue', NA, 2, "integer",
- 'hasHeaders', 'h', 2, "logical"
-), ncol=4, byrow=TRUE);
-opts = getopt(spec, commandArgs(trailingOnly = TRUE));
-
-if ( is.null(opts$xLabel ) ) { opts$xLabel = "" }
-if ( is.null(opts$plotTitle ) ) { opts$plotTitle = "" }
-if ( is.null(opts$hasHeaders ) ) { opts$hasHeaders = TRUE }
-
-df <- read.table(opts$inputFile, quote="\"", header = opts$hasHeaders);
-
-#echo "Generating Histogram"
-
-colName <-names(df)[opts$colIdx];
-
-if ( !is.null(opts$maxValue)) {
- message(paste0("combining all values greater than: ", opts$maxValue));
-
- df[colName][df[colName] > opts$maxValue] <- opts$maxValue
-}
-
-P<-ggplot(df,aes_string(x=colName)) +
- ggtitle(opts$plotTitle) +
- #scale_y_continuous(limits=c(0,2),labels=c("0.0","0.5","1.0","1.5","2.0")) +
- geom_histogram(binwidth = opts$binWidth) +
- theme(
- #axis.text.x = element_blank(),
- plot.margin = unit(c(0.3,0.3,0.3,0.3),"in"),
- plot.title = element_text(size=14,vjust=2),
- axis.title.x = element_text(size=14,vjust=-1),
- axis.title.y = element_text(size=14,vjust=2),
- strip.text.x = element_text(size = 12,face="bold")) +
- xlab(opts$xLabel) +
- ylab("Count")
-
-
-png(opts$outputFile,width=880, height=680)
-print(P);
-dev.off();
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/external/basicScatter.r b/SequenceAnalysis/resources/external/basicScatter.r
deleted file mode 100644
index 5789b4cee..000000000
--- a/SequenceAnalysis/resources/external/basicScatter.r
+++ /dev/null
@@ -1,55 +0,0 @@
-options(warn = -1)
-
-library(reshape)
-library(lattice)
-library(plyr)
-library(ggplot2)
-library(grid)
-library(perm)
-library(gridExtra)
-library(naturalsort)
-
-library(getopt);
-library(Matrix);
-
-options(scipen=1000000000)
-
-spec <- matrix(c(
- 'inputFile', 'i', 1, "character",
- 'outputFile', 'o', 1, "character",
- 'plotTitle', 't', 2, "character",
- 'xLabel', NA, 2, "character",
- 'xColIdx', 'x', 1, "integer",
- 'yColIdx', 'y', 1, "integer",
- 'hasHeaders', 'h', 2, "logical"
-), ncol=4, byrow=TRUE);
-opts = getopt(spec, commandArgs(trailingOnly = TRUE));
-
-if ( is.null(opts$xLabel ) ) { opts$xLabel = "" }
-if ( is.null(opts$plotTitle ) ) { opts$plotTitle = "" }
-if ( is.null(opts$hasHeaders ) ) { opts$hasHeaders = TRUE }
-
-df <- read.table(opts$inputFile, quote="\"", header = opts$hasHeaders);
-
-#echo "Generating Plot"
-
-xColName <-names(df)[opts$xColIdx];
-yColName <-names(df)[opts$yColIdx];
-
-P<-ggplot(df,aes_string(x=xColName, y=yColName)) +
- ggtitle(opts$plotTitle) +
- geom_point(shape=1) +
- theme(
- #axis.text.x = element_blank(),
- plot.margin = unit(c(0.3,0.3,0.3,0.3),"in"),
- plot.title = element_text(size=14,vjust=2),
- axis.title.x = element_text(size=14,vjust=-1),
- axis.title.y = element_text(size=14,vjust=2),
- strip.text.x = element_text(size = 12,face="bold")) +
- xlab(opts$xLabel) +
- ylab("Count")
-
-
-png(opts$outputFile,width=880, height=680)
-print(P);
-dev.off();
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/external/coverageGraph.r b/SequenceAnalysis/resources/external/coverageGraph.r
deleted file mode 100644
index 2fb7af566..000000000
--- a/SequenceAnalysis/resources/external/coverageGraph.r
+++ /dev/null
@@ -1,64 +0,0 @@
-library(reshape)
-library(lattice)
-library(plyr)
-library(ggplot2)
-library(grid)
-library(perm)
-library(gridExtra)
-library(naturalsort)
-
-library(getopt);
-library(Matrix);
-
-spec <- matrix(c(
- 'colHeader', '-c', 1, "character",
- 'outputFile', '-o', 1, "character",
- 'inputFile', '-i', 1, "character",
- 'plotTitle', '-t', 1, "character",
- 'vertical', '-v', 1, "integer",
- 'yLabel', NA, 1, "character"
-), ncol=4, byrow=TRUE);
-opts = getopt(spec, commandArgs(trailingOnly = TRUE));
-if ( is.null(opts$vertical ) ) { opts$vertical = 0 }
-
-df <- read.table(opts$inputFile, quote="\"", header = TRUE, fill = TRUE, na.strings = "NA");
-df$SequenceName <- factor(df$SequenceName, levels = naturalsort(unique(df$SequenceName)));
-
-df <- df[(!is.na(df[opts$colHeader])),];
-#str(df)
-
-plotHeight <- 680;
-
-if (opts$vertical == 1){
- facet1 <- 'SequenceName';
- facet2 <- '.';
- fac_formula <- as.formula(paste(facet1,"~",facet2))
- facetLine <- facet_grid(fac_formula, scales="free", space="fixed")
-
- plotHeight <- (500 * nlevels(df$SequenceName));
-} else {
- facet1 <- '.';
- facet2 <- 'SequenceName';
- fac_formula <- as.formula(paste(facet1,"~",facet2))
- facetLine <- facet_grid(fac_formula, scales="free", space="free")
-}
-
-# make all chroms plot
-P<-ggplot(df,aes_string(x="Start",y=opts$colHeader)) +
- ggtitle(opts$plotTitle) +
- #scale_y_continuous(limits=c(0,2),labels=c("0.0","0.5","1.0","1.5","2.0")) +
- geom_point(stat='identity') +
- theme(axis.text.x = element_blank(),
- plot.margin = unit(c(0.3,0.3,0.3,0.3),"in"),
- plot.title = element_text(size=14,vjust=2),
- axis.title.x = element_text(size=14,vjust=-1),
- axis.title.y = element_text(size=14,vjust=2),
- strip.text.x = element_text(size = 12,face="bold")) +
- xlab("Position") +
- ylab(opts$yLabel) +
- facetLine
-
-
-png(opts$outputFile,width=880, height=plotHeight)
-print(P);
-dev.off();
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/external/fastqc/Configuration/adapter_list.txt b/SequenceAnalysis/resources/external/fastqc/Configuration/adapter_list.txt
index 63d7ff601..236dca897 100644
--- a/SequenceAnalysis/resources/external/fastqc/Configuration/adapter_list.txt
+++ b/SequenceAnalysis/resources/external/fastqc/Configuration/adapter_list.txt
@@ -20,5 +20,8 @@
# fragments for now.
Illumina Universal Adapter AGATCGGAAGAG
-Illumina Small RNA Adapter ATGGAATTCTCG
-Nextera Transposase Sequence CTGTCTCTTATA
\ No newline at end of file
+Illumina Small RNA 3' Adapter TGGAATTCTCGG
+Illumina Small RNA 5' Adapter GATCGTCGGACT
+Nextera Transposase Sequence CTGTCTCTTATA
+PolyA AAAAAAAAAAAA
+PolyG GGGGGGGGGGGG
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/external/fastqc/Configuration/contaminant_list.txt b/SequenceAnalysis/resources/external/fastqc/Configuration/contaminant_list.txt
index eb4b70a83..1ae0bd980 100644
--- a/SequenceAnalysis/resources/external/fastqc/Configuration/contaminant_list.txt
+++ b/SequenceAnalysis/resources/external/fastqc/Configuration/contaminant_list.txt
@@ -43,7 +43,6 @@ Illumina NlaIII expression Sequencing Primer CCGACAGGTTCAGAGTTCTACAGTCCGACATG
Illumina Small RNA Adapter 1 GTTCAGAGTTCTACAGTCCGACGATC
Illumina Small RNA Adapter 2 TGGAATTCTCGGGTGCCAAGG
Illumina Small RNA RT Primer CAAGCAGAAGACGGCATACGA
-Illumina Small RNA PCR Primer 1 CAAGCAGAAGACGGCATACGA
Illumina Small RNA PCR Primer 2 AATGATACGGCGACCACCGACAGGTTCAGAGTTCTACAGTCCGA
Illumina Small RNA Sequencing Primer CGACAGGTTCAGAGTTCTACAGTCCGACGATC
@@ -84,14 +83,11 @@ Illumina NlaIII Gex PCR Primer 1 CAAGCAGAAGACGGCATACGA
Illumina NlaIII Gex PCR Primer 2 AATGATACGGCGACCACCGACAGGTTCAGAGTTCTACAGTCCGA
Illumina NlaIII Gex Sequencing Primer CCGACAGGTTCAGAGTTCTACAGTCCGACATG
-Illumina Small RNA RT Primer CAAGCAGAAGACGGCATACGA
Illumina 5p RNA Adapter GTTCAGAGTTCTACAGTCCGACGATC
Illumina RNA Adapter1 TGGAATTCTCGGGTGCCAAGG
Illumina Small RNA 3p Adapter 1 ATCTCGTATGCCGTCTTCTGCTTG
Illumina Small RNA PCR Primer 1 CAAGCAGAAGACGGCATACGA
-Illumina Small RNA PCR Primer 2 AATGATACGGCGACCACCGACAGGTTCAGAGTTCTACAGTCCGA
-Illumina Small RNA Sequencing Primer CGACAGGTTCAGAGTTCTACAGTCCGACGATC
TruSeq Universal Adapter AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT
TruSeq Adapter, Index 1 GATCGGAAGAGCACACGTCTGAACTCCAGTCACATCACGATCTCGTATGCCGTCTTCTGCTTG
@@ -115,7 +111,7 @@ TruSeq Adapter, Index 19 GATCGGAAGAGCACACGTCTGAACTCCAGTCACGTGAAACTCTCGTATGC
TruSeq Adapter, Index 20 GATCGGAAGAGCACACGTCTGAACTCCAGTCACGTGGCCTTCTCGTATGCCGTCTTCTGCTTG
TruSeq Adapter, Index 21 GATCGGAAGAGCACACGTCTGAACTCCAGTCACGTTTCGGTCTCGTATGCCGTCTTCTGCTTG
TruSeq Adapter, Index 22 GATCGGAAGAGCACACGTCTGAACTCCAGTCACCGTACGTTCTCGTATGCCGTCTTCTGCTTG
-TruSeq Adapter, Index 23 GATCGGAAGAGCACACGTCTGAACTCCAGTCACCGTACGTTCTCGTATGCCGTCTTCTGCTTG
+TruSeq Adapter, Index 23 GATCGGAAGAGCACACGTCTGAACTCCAGTCACCCACTCTTCTCGTATGCCGTCTTCTGCTTG
TruSeq Adapter, Index 25 GATCGGAAGAGCACACGTCTGAACTCCAGTCACACTGATATCTCGTATGCCGTCTTCTGCTTG
TruSeq Adapter, Index 27 GATCGGAAGAGCACACGTCTGAACTCCAGTCACATTCCTTTCTCGTATGCCGTCTTCTGCTTG
@@ -180,3 +176,11 @@ ABI Solid3 EF1 alpha Sense Primer CATGTGTGTTGAGAGCTTC
ABI Solid3 EF1 alpha Antisense Primer GAAAACCAAAGTGGTCCAC
ABI Solid3 GAPDH Forward Primer TTAGCACCCCTGGCCAAGG
ABI Solid3 GAPDH Reverse Primer CTTACTCCTTGGAGGCCATG
+
+
+
+Clontech Universal Primer Mix Short CTAATACGACTCACTATAGGGC
+Clontech Universal Primer Mix Long CTAATACGACTCACTATAGGGCAAGCAGTGGTATCAACGCAGAGT
+Clontech SMARTer II A Oligonucleotide AAGCAGTGGTATCAACGCAGAGTAC
+Clontech SMART CDS Primer II A AAGCAGTGGTATCAACGCAGAGTACT
+
diff --git a/SequenceAnalysis/resources/external/fastqc/Configuration/limits.txt b/SequenceAnalysis/resources/external/fastqc/Configuration/limits.txt
index 742d172cc..ec4280c1a 100644
--- a/SequenceAnalysis/resources/external/fastqc/Configuration/limits.txt
+++ b/SequenceAnalysis/resources/external/fastqc/Configuration/limits.txt
@@ -2,7 +2,7 @@
# module at all by setting the value below to 1 for the
# modules you want to remove.
duplication ignore 0
-kmer ignore 0
+kmer ignore 1
n_content ignore 0
overrepresented ignore 0
quality_base ignore 0
diff --git a/SequenceAnalysis/resources/external/fastqc/INSTALL.txt b/SequenceAnalysis/resources/external/fastqc/INSTALL.txt
deleted file mode 100644
index f55db8b08..000000000
--- a/SequenceAnalysis/resources/external/fastqc/INSTALL.txt
+++ /dev/null
@@ -1,127 +0,0 @@
-Installing FastQC
--------------------
-FastQC is a java application. In order to run it needs your system to have a suitable
-Java Runtime Environment (JRE) installed. Before you try to run FastQC you should therefore
-ensure that you have a suitable JRE. There are a number of different JREs available
-however the one we have tested is the v1.6 JRE from Oracle. This is available
-for a number of different platforms from www.java.com (click the download now button at the
-top).
-
-If you're not sure whether you have java installed then you can test this from a command
-prompt. To get a command prompt try:
-
-Windows: Select Start > Run, and type 'cmd' (no quotes) in the box which appears, press OK
-
-MaxOSX: Run Applications > Utilities > Terminal
-
-Linux: From your applications menu look for an application called 'Terminal' or 'Konsole'.
-Either of these will give you a usable shell.
-
-At the command prompt type 'java -version' and press enter. You should see something like:
-
-java version "1.6.0_17"
-Java(TM) SE Runtime Environment (build 1.6.0_17-b04-248-10M3025)
-Java HotSpot(TM) Client VM (build 14.3-b01-101, mixed mode)
-
-If you get an error then you don't have java installed. If the version listed on the first
-line is less than 1.5 then you might have problems running FastQC.
-
-Actually installing FastQC is as simple as unzipping the zip file it comes in into a
-suitable location. That's it. Once unzipped it's ready to go.
-
-Running FastQC
---------------
-
-You can run FastQC in one of two modes, either as an interactive graphical application
-in which you can dynamically load FastQ files and view their results.
-
-Alternatively you can run FastQC in a non-interactive mode where you specify the files
-you want to process on the command line and FastQC will generate an HTML report for
-each file without launching a user interface. This would allow FastQC to be run as
-part of an analysis pipeline.
-
-
-Running FastQC Interactively
-----------------------------
-Windows: Simply double click on the run_fastqc bat file. If you want to make a pretty
-shortcut then we've included an icon file in the top level directory so you don't have
-to use the generic bat file icon.
-
-MacOSX: There is an application bundle for MacOSX which you can use to install and run
-FastQC. Just drag the application from the disk image to your Applications folder (or
-wherever you want to install the program).
-
-Linux: We have included a wrapper script, called 'fastqc' which is the easiest way to
-start the program. The wrapper is in the top level of the FastQC installation. You
-may need to make this file executable:
-
-chmod 755 fastqc
-
-..but once you have done that you can run it directly
-
-./fastqc
-
-..or place a link in /usr/local/bin to be able to run the program from any location:
-
-sudo ln -s /path/to/FastQC/fastqc /usr/local/bin/fastqc
-
-
-Running FastQC as part of a pipeline
-------------------------------------
-To run FastQC non-interactively you should use the fastqc wrapper script to launch
-the program. You will probably want to use the zipped install file on every platform
-(even OSX).
-
-To run non-interactively you simply have to specify a list of files to process
-on the commandline
-
-fastqc somefile.txt someotherfile.txt
-
-You can specify as many files to process in a single run as you like. If you don't
-specify any files to process the program will try to open the interactive application
-which may result in an error if you're running in a non-graphical environment.
-
-There are a few extra options you can specify when running non-interactively. Full
-details of these can be found by running
-
-fastqc --help
-
-By default, in non-interactive mode FastQC will create both a zipped copy of the
-QC report, and also extract this to create a folder which contains the report
-files ready to be viewed. If you only want to create the zipped file then you can
-add
-
---noextract
-
-To the launch command to suppress the unzipping.
-
-If you want to save your reports in a folder other than the folder which contained
-your original FastQ files then you can specify an alternative location by setting a
---outdir value:
-
---outdir=/some/other/dir/
-
-Customising the report output
------------------------------
-
-If you want to run FastQC as part of a sequencing pipeline you may wish to change the
-formatting of the report to add in your own branding or to include extra information.
-
-In the Templates directory you will find a file called 'header_template.html' which
-you can edit to change the look of the report. This file contains all of the header for
-the report file, including the CSS section and you can alter this however you see fit.
-
-If you want to add in your own logo or other image files to the reports then you can drop
-a png or jpg file into the Icons folder in the templates directory and this will be copied
-into the report folder for all reports generated by the program. You can refer to these
-icons using a relative URL (eg Icons/image.png) in the HTML template. Images placed
-outside the icons directory will not be copied.
-
-Whilst you can make whatever changes you like you should probably leave in place the
-
structure of the html template since later code will expect to close the main div
-which is left open at the end of the header. There is no facility to change the code in
-the main body of the report or the footer (although you can of course change the styling).
-
-The text tags @@FILENAME@@ and @@DATE@@ are placeholders which are filled in when the
-report it created. You can use these placeholders in other parts of the header if you
-wish.
diff --git a/SequenceAnalysis/resources/external/fastqc/LICENSE b/SequenceAnalysis/resources/external/fastqc/LICENSE
new file mode 100644
index 000000000..94a9ed024
--- /dev/null
+++ b/SequenceAnalysis/resources/external/fastqc/LICENSE
@@ -0,0 +1,674 @@
+ GNU GENERAL PUBLIC LICENSE
+ Version 3, 29 June 2007
+
+ Copyright (C) 2007 Free Software Foundation, Inc.
+ Everyone is permitted to copy and distribute verbatim copies
+ of this license document, but changing it is not allowed.
+
+ Preamble
+
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+software and other kinds of works.
+
+ The licenses for most software and other practical works are designed
+to take away your freedom to share and change the works. By contrast,
+the GNU General Public License is intended to guarantee your freedom to
+share and change all versions of a program--to make sure it remains free
+software for all its users. We, the Free Software Foundation, use the
+GNU General Public License for most of our software; it applies also to
+any other work released this way by its authors. You can apply it to
+your programs, too.
+
+ When we speak of free software, we are referring to freedom, not
+price. Our General Public Licenses are designed to make sure that you
+have the freedom to distribute copies of free software (and charge for
+them if you wish), that you receive source code or can get it if you
+want it, that you can change the software or use pieces of it in new
+free programs, and that you know you can do these things.
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+these rights or asking you to surrender the rights. Therefore, you have
+certain responsibilities if you distribute copies of the software, or if
+you modify it: responsibilities to respect the freedom of others.
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+.
diff --git a/SequenceAnalysis/resources/external/fastqc/Main.txt b/SequenceAnalysis/resources/external/fastqc/Main.txt
deleted file mode 100644
index aad1ee48a..000000000
--- a/SequenceAnalysis/resources/external/fastqc/Main.txt
+++ /dev/null
@@ -1 +0,0 @@
-Main-Class: uk.ac.bbsrc.babraham.FastQC.FastQCApplication
diff --git a/SequenceAnalysis/resources/external/fastqc/README.txt b/SequenceAnalysis/resources/external/fastqc/README.txt
deleted file mode 100644
index e08d5a2f0..000000000
--- a/SequenceAnalysis/resources/external/fastqc/README.txt
+++ /dev/null
@@ -1,42 +0,0 @@
-FastQC - A Quality Control application for FastQ files
-------------------------------------------------------
-
-Most high throughput sequencers generate output in FastQ format. This
-format combines the base calls for the sequence which was generated with
-an encoded quality value for each base which says how confident the
-sequencer was that the base call generated was correct.
-
-Before proceeding with the analysis of a sequence data set it is
-a good idea to do some basic quality control checks on the raw data
-to ensure that there are no hidden problems which might be more
-difficult to detect at a later stage.
-
-FastQC is an application which takes a FastQ file and runs a series
-of tests on it to generate a comprehensive QC report. This will
-tell you if there is anything unusual about your sequence. Each
-test is flagged as a pass, warning or fail depending on how far it
-departs from what you'd expect from a normal large dataset with no
-significant biases. It's important to stress that warnings or even
-failures do not necessarily mean that there is a problem with your
-data, only that it is unusual. It is possible that the biological
-nature of your sample means that you would expect this particular
-bias in your results.
-
-FastQC can be run either as an interactive graphical application
-which allows you to view results for multiple files in a single
-application. Alternatively you can run the program in a non
-interactive way (say as part of a pipeline) which will generate
-an HTML report for each file you process.
-
-FastQC is a cross-platform application, written in java. In theory it
-should run on any platform which has a suitable java runtime environment.
-Having said that we've only tested in on Windows, MacOSX 10.6 and Linux
-running the Sun v1.5 and 1.6 JREs. Please let us know what happened if
-you try running it on other platforms / JREs.
-
-If you have any comments about FastQC we would like to hear them. You
-can either enter them in our bug tracking system at:
-
-http://www.bioinformatics.bbsrc.ac.uk/bugzilla/
-
-..or send them directly to simon.andrews@bbsrc.ac.uk.
diff --git a/SequenceAnalysis/resources/external/fastqc/RELEASE_NOTES.txt b/SequenceAnalysis/resources/external/fastqc/RELEASE_NOTES.txt
deleted file mode 100644
index 1e41c2c81..000000000
--- a/SequenceAnalysis/resources/external/fastqc/RELEASE_NOTES.txt
+++ /dev/null
@@ -1,613 +0,0 @@
-RELEASE NOTES FOR FastQC V0.10.0
---------------------------------
-
-The major feature of FastQC v0.10.0 is the addition of support
-for fastq files generated directly by the latest version of the
-illumina pipeline (Casava v1.8). In this version the pipeline
-generates gzipped fastq files by default rather than using qseq
-files which can then be converted to fastq. However the fastq
-files generated by casava are unusual in two ways:
-
-1) A single sample produces a set of fastq files with a common
- name, but an incrementing number at the end.
-
-2) Casava FastQ files contain sequences from clusters which have
- failed the internal QC, and been flagged to be filtered.
-
-FastQC v0.10.0 introduces a Casava mode which will merge together
-fastq files from the same sample group and produce a single report.
-It will also exclude any flagged entries from the analysis. You
-would therefore run FastQC as normal but selecting all of the
-fastq files from Casava and using casava mode for your analysis.
-
-Casava mode is activated from the command line by adding the
---casava option to the launch command. From the interactive
-application you need to select 'Casava FastQ Files' from the drop
-down file selector filter options.
-
-If you want to analyse casava fastq files without these extra
-options then you can use treat them as normal fastq files with
-no problems.
-
-In addition to this change there have also been changes to allow
-the wrapper script to work properly under windows, and a bug was
-fixed which missed of the last possible Kmer from every sequence
-in a library.
-
-
-RELEASE NOTES FOR FastQC V0.9.6
--------------------------------
-
-FastQC v0.9.6 fixes a couple of bugs which aren't likely to have
-affected the majority of fastqc users:
-
-- Fixed a crash in the Kmer module when analysing a sequence where
- every sequence in a library contained a poly-N stretch at its
- 3' end.
-
-- Fixed the wrapper script so that OSX users launching fastqc
- through the script rather than the Mac application bundle get
- their classpath set correctly, and can therefore analyse bam/sam
- files.
-
-
-RELEASE NOTES FOR FastQC V0.9.5
--------------------------------
-
-FastQC v0.9.5 fixes some bugs in the programs text output and
-improves a few things in the graphical interface. Main changes
-are:
-
-- Progress calculations are now exact and not approximate
-
-- The UI now has a welcome screen so you're not just presented
- with a blank screen when the program starts
-
-- The wrapper script now sets the classpath correctly in windows
- as well as linux.
-
-- The text report for per-base sequence content now reports
- correct values for grouped bases
-
-- The HTML report uses a custom stylesheet for print output so
- graphs aren't cut off when reports are printed.
-
-- Fixed a bug in testing for a warning in the per-base sequence
- content module.
-
-- Alt text in HTML reports now matches the graphic it describes
-
-
-RELEASE NOTES FOR FastQC V0.9.4
--------------------------------
-
-FastQC v0.9.4 is a minor bugfix release which changes the offline
-version of the program so that if a file fails to be processed a
-full backtrace of the error is produced, rather than just a
-simple generic error message.
-
-RELEASE NOTES FOR FastQC V0.9.3
--------------------------------
-
-FastQC v0.9.3 adds support for fastq files compressed with
-bzip2 in addition to its existing support for gzip compressed
-files. It's worth noting that although bzip2 offers a reduction
-in the file size of the compressed files (about a 5-fold size
-reduction compared to raw fastq. Gzip is a 4-fold decrease),
-there is a significant penalty in terms of the speed of
-decompression of these files. In our tests gzipped files were
-actually processed slightly faster than raw FastQ files, presumably
-due to the lower amount of data transfer from disk required,
-however bzip2 compressed files took around 6X as long to
-process as gzipped files.
-
-The other big change in this release is an update to the default
-CSS layout such that viewing the HTML reports doesn't require
-lots of scrolling up and down the page. As before the CSS can
-be edited and customised by editing the templates shipped with
-the program. Many thanks to Phil Ewels who did much of the
-work on the new layout.
-
-
-
-RELEASE NOTES FOR FastQC V0.9.2
--------------------------------
-
-FastQC v0.9.2 fixes two bugs which were identified in the
-previous release.
-
-1) In the text output for the per-base quality module the
-correct base numbers weren't being included for files which
-used grouped base ranges.
-
-2) The Kmer analysis module could crash when analysing very
-small files, such that no position in the file had more than
-1000 instances of an enriched Kmer.
-
-Both of these issues should now be resolved.
-
-
-RELEASE NOTES FOR FastQC V0.9.1
--------------------------------
-
-FastQC v0.9.1 adds some new command line options and fixes a
-couple of usability issues.
-
-The new command line options are:
-
---quiet Will suppress all progress messages and ensure that only
-warnings or errors are written to stderr. This might be useful
-for people running fastqc as part of a pipeline.
-
---nogroup Will turn off the dynamic grouping of bases in the
-various per-base plots. This would allow you to see a result
-for each base of a 100bp run for example. This option should
-not be used for really long reads (454, PacBio etc) since it
-has the potential to crash the program or generate very wide
-output plots
-
-In addition to these the following changes have been made:
-
-The basic stats module now includes a line to say which type
-of quality encoding was found so this information isn't just
-present in the header of the per-base quality plot, and will
-appear in the text based output.
-
-We now distinguish between Illumina <1.3, 1.3 and 1.5 encodings
-rather than just <1.3 and >=1.3. The Sanger encoding is now
-labelled as Sanger / Illumina 1.9+ to allow for the change in
-encoding in the latest illumina pipeline.
-
-A bug was fixed which caused the program to crash when encountering
-a zero length colorspace file (which shouldn't happen anyway, but
-crashing wasn't the correct response).
-
-The interactive over-represented sequence table now allows you
-to copy out each cell individually which makes it easy to copy
-any unknown sequences into other programs.
-
-
-RELEASE NOTES FOR FastQC V0.9.0
--------------------------------
-
-FastQC v0.9.0 makes a number of changes primarily targetted at
-datasets containing longer reads. It allows all of the analyses
-within FastQC to be completed sensibly and without excessive
-resource usage on runs containing reads up to tens of kilobases
-in length.
-
-For long reads the program now converts many of its plots to
-variably sized bins so that, for example you see every base for
-the first 10 bases, then every 5 bases for the next 40 bases,
-then every 50, then 100 then 1kb per bin, until the end of the
-sequence is reached. For sequences below 75bp the reports will
-look exactly the same as before. For groups running slightly
-longer Illumina or ABI runs you'll see some compression at the
-end of your reads, and people using 454 or PacBio will get
-sensible results for all analyses for the first time.
-
-One additional change which will impact anyone using reads over
-75bp is that the duplicate sequence and overrepresented sequence
-plots now only use the first 50bp of each read if the total read
-length is over 75bp. This is because these plots work on the
-basis of an exact sequence match, and longer reads tend to show
-more errors at the end which makes them look like different
-sequences when they're actually the same. 50bp should be enough
-that you won't see exact matches by chance.
-
-
-
-RELEASE NOTES FOR FastQC V0.8.0
--------------------------------
-
-FastQC v0.8.0 adds some new options for parsing BAM/SAM files and
-makes the graphs in the report easier to interpret.
-
-All graphs in v0.8.0 now have marker lines going across them to make
-it easier to relate the data in the graph to the y-axis. The per
-base quality boxplots have shading behind the graph to indicate ranges
-of good, medium and bad quality sequence.
-
-For BAM/SAM files you can now specify that you wish to analyse only
-the mapped sequences in the file. This is particularly of use to
-people working on colorspace data where the mapped data should
-produce reliable sequence, whereas the current raw conversion to
-base space may overrepresent any errors which are present. The
-option to use only mapped data is set by using the
-
--f bam_mapped or -f sam_mapped
-
-option on the command line, or by specifying Mapped BAM/SAM files
-from the drop down file filter in the file chooser in the interactive
-version of the program.
-
-For FastQ files the parser has been updated to not treat blank lines
-between entries or at the end of the file as a format violation since
-many sequences in the public repositories can have this problem.
-
-From the command line we now offer the option to process multiple
-files in parallel by setting the -t/--threads option. Please note that
-using more than 1 thread will increase the amount of allocated memory
-(250MB per thread), so you need to be sure you have enough memory (and
-disk bandwidth) to be able to process more than one file. The
-interactive application still defaults to a single processing thread
-but you could theoretically change this by passing the correct java
-properties in the startup command.
-
-
-RELEASE NOTES FOR FastQC V0.7.2
--------------------------------
-
-FastQC v0.7.2 fixes a bug in libraries where no unique sequences
-were observed. It also improves the collection of duplicate
-statistics on libraries with very low diversity.
-
-A new command line option has been added to allow the user to
-manually specify a contaminant's file rather than using the sitewide
-default. This would be useful if you have different sets of
-contaminants to screen against for different libraries, or if you
-wanted to make a custom set of contaminants, but didn't have
-sufficient privileges to modify the sitewide contaminants file.
-
-
-RELEASE NOTES FOR FastQC V0.7.1
--------------------------------
-
-FastQC v0.7.1 makes some significant enhancements to the fastqc
-wrapper script which make it easier to use as part of a pipeline.
-
-You can now use normal unix options to create your fastqc
-command rather than having to pass java system properties. The
-old options will continue to work though, so the updated
-wrapper is still compatible with any previous commands you may
-have in place. Full details of the new options can be found
-by running
-
-fastqc --help
-
-One new option is the --format option which allows you to manually
-specify the input format of a file, rather than having FastQC
-guess the format from the file name. This would allow you to have
-a BAM file called test.dat and process it using:
-
-fastqc --format bam test.dat
-
-
-
-
-RELEASE NOTES FOR FastQC V0.7.0
--------------------------------
-
-FastQC v0.7.0 introduces a new analysis module which looks at the
-enrichment of short sequences within the library. It is possible
-to get enrichment of unaligned subsequences to quite a high degree
-without this being apparent in any of the existing modules. This
-new module should find problems such as read through into the
-adapters at the other end of libraries, which other analyses would
-miss.
-
-Other changes in this release include:
-
-* Altering the fastqc wrapper script so it can identify when it's
- being used on the source distribution of the software so it can
- issue an appropriate warning.
-
-* Tidied up all of the y-axes on the graphs so that scaling should
- now always be perfect in all graphs.
-
-
-RELEASE NOTES FOR FastQC V0.6.1
--------------------------------
-
-FastQC v0.6.1 is a bugfix release which fixes a problem with sequences
-from BAM/SAM files which map to the reverse strand of the reference.
-
-In these cases the sequence contained in the BAM/SAM file is reverse
-complemented and the qualities are reversed relative to the original
-sequence which came off the sequencer. In the previous release this
-meant that the plots were incorrectly showing a mix of forward and
-reversed sequences.
-
-In v0.6.1 any sequences mapping to the reverse strand of the reference
-are converted back to their original state before being analysed which
-should give a clearer view of the overall qualities and sequence biases
-within the run.
-
-
-RELEASE NOTES FOR FastQC V0.6.0
--------------------------------
-
-FastQC v0.6 adds support for reading SAM/BAM files as well as still
-supporting fastq files. File type detection is based on the filename
-so SAM/BAM files need to be named .sam or .bam. Any other form of
-filename is assumed to be a fastq file.
-
-SAM/BAM reading was added through the use of the picard libraries, which
-means that the launcher for FastQC has had to be modified to include
-the picard libraries into the classpath. If you use the bat file launcher,
-the wrapper script or the Mac application bundle then you won't need to
-do anything to get the new version to work, but if you've created your
-own launcher then you will need to modify your classpath statement to
-include the sam-1.32.jar file into the classpath.
-
-The only other change in this release is that the line graphs have been
-improved to use smoother lines for the graphs.
-
-
-
-RELEASE NOTES FOR FastQC V0.5.1
--------------------------------
-
-Release 0.5.1 fixes a couple of bugs and makes some improvements to
-existing functions.
-
-* A bug was fixed which caused the headers of the overrepresented
- sequences results to not be separated in the text output.
-
-* A bug was fixed which caused spikes to appear in the %GC profile
- when using read lengths >100bp
-
-* The fitting of the theoretical distribution to the %GC profile
- was improved
-
-* Some new entries were added to the contaminants file to cover
- Illumina oligos for multiplexing, tag expression and small RNA
- protocols (thanks to Aaron Statham for providing these)
-
-
-RELEASE NOTES FOR FastQC V0.5.0
--------------------------------
-
-FastQC v0.4.4 makes a number of changes to the previous
-release which hopefully improve the relevance of the output.
-
-* The fitting of the normal curve to the %GC distribution has
- been improved for shorter sequences
-
-* Each section of the HTML report output now has a pass/warn/fail
- icon next to it, rather than just having them at the top
-
-* The duplicate level analysis now estimates the total percentage
- of sequences which are not unique, reports this on the graph and
- uses this as the basis for the pass/warn/fail filtering
-
-* The structure of the HTML output folder has been changed so that
- icons and images are put into subfolders so the only files at
- the top level are ones which the user is intended to open directly.
-
-
-RELEASE NOTES FOR FastQC V0.4.3
--------------------------------
-
-FastQC v0.4.3 is a bugfix release which fixes a bug and adds
-an extra check to the interactive program.
-
-In versions of the program since v0.2 the total sequence count
-in the Basic Stats module may have been incorrect by a few percent
-(either high or low). This is because instead of using the real
-sequence count the module was using an estimated count which should
-only be used for updating the progress indicators. The module
-has now been fixed to report the actual sequence count.
-
-In the interactive application there was no warning given if you
-chose to save a report and opted to overwrite an existing report. You
-will now be warned in this case an offered the chance to use a
-different filename. This change won't affect the non-interactive
-mode of the program where report files will be overwritten if the
-program is run more than once on the same set of data.
-
-RELEASE NOTES FOR FastQC V0.4.2
--------------------------------
-
-FastQC v0.4.2 is a minor release which fixes some bugs and improves
-the warnings on some of the analysis modules.
-
-Bugs which were fixed were:
-
-* The per-base quality plot showed an incorrect scale on the
- y-axis. This was usually off by about 2, but could be more
- depending on the data. The relative relationships shown
- were correct, it was just the scale bar which was wrong.
-
-* The sequence parser incorrectly identified some base called
- files as colorspace files where they contained dots in place
- of N base calls. This has now been improved but will still
- fail for the base where a base called file starts with an
- entry which is a single called base followed by all dots
- since this is indistinguishable from a colorspace fastq file.
-
-* Some JREs (notably OpenJDK) can't cope with a headless environment
- being set from within the program. I've therefore added code
- to the fastqc wrapper script to externally set the headless
- environment up to bypass this problem.
-
-Other improvements which have been made are:
-
-* When writing out graphs for the HTML report we now scale some
- graphs by the length of the sequences analysed so we don't get
- really squashed graphs. The interactive application will still
- scale the graphs to the size of the window
-
-* More checks have been added to the parsing of FastQ files to
- ensure we're looking at the correct file format. A better reporting
- mechanism has been added to allow the program to cope better with
- problems during parsing.
-
-* The per-sequence GC plot has been modified to add in a modelled
- normal distribtion over the observed distribution so you can see
- how well the two fit.
-
-* All modules (apart from the general stats) now have valid checks
- in place, and all can now produce warnings and failures. Some of
- the checks in the existing modules have been changed to better cope
- with libraries with very low or high GC content.
-
-
-RELEASE NOTES FOR FastQC V0.4.1
--------------------------------
-
-FastQC v0.4.1 is a bugfix release which changes the operation
-of the duplicate sequence and overrepresented sequence modules.
-
-Both of these modules now only track sequences which appear in
-the first 200,000 sequences of a file. This change was made
-because people using longer read lengths found that tracking
-the first million sequences led to the program exhausting its
-allocated memory.
-
-The other change is that the duplicate sequence module now
-tracks sequence counts to the end of the file rather than
-stopping after a million sequences. This means the final
-duplication counts seen are much more realistic and should
-match with what you would see in a genome browser. Because
-of this change the cutoffs to flag a file with a warning or
-an error have been increased. You now get a warning when
-the sum of duplicated sequences is more than 20% of the
-unique sequences. You get an error when there are more
-duplicated sequences than unique sequences.
-
-
-RELEASE NOTES FOR FastQC V0.4
------------------------------
-
-FastQC v0.4 introduces a new analysis module, and easier way
-to launch the program from the command line and a new output
-file, as well as fixing a few minor bugs.
-
-The new analysis module is the sequence duplication level
-module. This is a complement to the existing overrepresented
-sequences module in that it looks at sequences which occur
-more than once in your data. The new module takes a more
-global view and says what proportion of all of your sequences
-occur once, twice, three times etc. In a diverse library most
-sequences should occur only once. A highly enriched library
-may have some duplication, but higher levels of duplication
-may indicate a problem, such as a PCR overamplification.
-
-In response to several requests we've also now introduced a
-new output file into the report. This is a text based, tab
-delimited file which includes all of the data show in the
-graphs in the graphical report. This would allow people
-running pipelines to store the data generated by fastQC and
-analyse it systematically rather than just taking the
-pass/fail/warn summary, or reviewing the reports manually.
-
-Finally, if you're running fastqc from the command line we've
-now included a 'fastqc' wrapper script which you can launch
-directly rather than having to construct a java launch
-command. You can still pass -Dxxx options through to the
-program, but for simple analyses you can now simply run:
-
-fastqc [some files]
-
-..once you have included the FastQC install directory into your
-path. More details are in the install document.
-
-Other minor changes:
-
-- The over-represented sequences module now scans the first
-million sequences to decide which sequences to track to the
-end of the file.
-
-- The labeling on the per-base N content graph is now correct
-
-
-
-RELEASE NOTES FOR FastQC V0.3.1
--------------------------------
-
-V0.3.1 is a bugfix release which fixes a few minor problems.
-
-1) The template system now correctly checks that it only imports
-graphics files from the templates directory into the report
-files and doesn't break when it encounters unexpected files.
-
-2) The offline mode now correctly reports the progress of all
-processed files rather than just the first one.
-
-3) The documentation has been updated to include information on
-the blue mean line in the per base quality plot.
-
-
-RELEASE NOTES FOR FastQC V0.3
------------------------------
-
-Major new additions to v0.3 are listed below:
-
-1) Support for gzip compressed fastq files. You can now
-load gzip compressed fastq files into FastQC in the same
-way as uncompressed files. The files will be decompressed
-interactively and can be viewed in the same way as for
-uncompressed files.
-
-2) Contaminant identification. If your library is found to
-have overrepresented sequences in it these are now scanned
-against a database of common contaminants (primers, adapters etc)
-to see if the source of the contamination can be identified.
-The database is stored in a new Contaminants folder in the
-main installation directory, and can be updated with your
-own protocol specific sequences.
-
-3) When in non-interactive mode you can now pass a
-preference -Dfastqc.output_dir to provide an alternative location
-to save reports to, rather than having them in the same
-directory as the source fastq files.
-
-Some improvements have also been made to the colorspace support
-so this version should support a wider range of colorspace
-fastq files.
-
-
-RELEASE NOTES FOR FastQC V0.2
------------------------------
-
-There are a few new additions in v0.2 of FastQC
-
-1) Colorspace support: We now have rudimentary support for the
-analysis of fastq files in colorspace. The analysis is done by
-converting the colorspace calls to basecalls, which isn't ideal
-but is hopefully more useful than nothing.
-
-2) Option to unzip reports. The default action in non-interactive
-mode is now to both create a zip file containing the FastQC report
-and to unzip this into a folder of the same name. If you just want
-to generate the zip files you can add -Dfastqc.unzip=false to the
-command line to suppress this new behaviour
-
-3) It is now possible to customise the HTML report for your site.
-There is an HTML template which can be edited to add your own
-branding to the reports you generate.
-
-4) In addition to the human readable HTML report we now also
-generate a tab delimited summary file which should make it
-easier to integrate FastQC into an automated reporting system
-which spots any potential problems with the data.
-
-
-RELEASE NOTES FOR FastQC V0.1.1
--------------------------------
-
-This point release fixes a problem when running FastQC in a
-non-interactive mode on a system without a graphical display.
-The program should now operate correctly on headless systems
-as long as the filename(s) to process are specified on the
-command line.
-
-
-RELEASE NOTES FOR FastQC V0.1
--------------------------------
-
-FastQC v0.1 is a beta release it should work in its present state but
-we are keen to get feedback on the program. In particular we are
-interested to hear if anyone has:
-
-1) Suggestions for other checks we could be performing.
-
-2) Comments about the criteria we set for issuing warnings or errors and
-suggestions for how these could be improved.
-
-You can report feedback either though our bug reporting tool at:
-
-www.bioinformatics.bbsrc.ac.uk/bugzilla/
-
-...or directly to simon.andrews@bbsrc.ac.uk
diff --git a/SequenceAnalysis/resources/external/fastqc/Templates/header_template.html b/SequenceAnalysis/resources/external/fastqc/Templates/header_template.html
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@@ -1,4 +1,3 @@
-
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@@ -7,10 +6,11 @@
-
-
+
+
-
+
+
\ No newline at end of file
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diff --git a/SequenceAnalysis/resources/external/jbzip2-0.9.jar b/SequenceAnalysis/resources/external/jbzip2-0.9.jar
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diff --git a/SequenceAnalysis/resources/external/qscript/IndelRealignerRunner.scala b/SequenceAnalysis/resources/external/qscript/IndelRealignerRunner.scala
deleted file mode 100644
index badb29148..000000000
--- a/SequenceAnalysis/resources/external/qscript/IndelRealignerRunner.scala
+++ /dev/null
@@ -1,35 +0,0 @@
-import org.broadinstitute.gatk.queue.QScript
-import org.broadinstitute.gatk.queue.extensions.gatk._
-
-class IndelRealignerRunner extends QScript {
-
- qscript =>
-
- // Required arguments. All initialized to empty values.
- @Input(doc="The reference file for the bam files.", shortName="R")
- var referenceFile: File = _ // _ is scala shorthand for null
-
- @Input(doc="One or more bam files.", shortName="I")
- var bamFiles: List[File] = Nil
-
- @Output(fullName = "output", shortName = "o", doc = "the output file")
- var output: File = _
-
- @Output(fullName = "targetIntervals", shortName = "targetIntervals", doc = "the intervals file output from RealignerTargetCreator")
- var targetIntervals: File = _
-
- @Argument(fullName="scatterCount", shortName="scatterCount", doc="the number of concurrent jobs", required=false)
- var scatterCount: Int = 1
-
- def script(){
- val realigner = new IndelRealigner
- realigner.R = this.referenceFile
- realigner.I = this.bamFiles
- realigner.out = this.output
- realigner.bam_compression = 9
- realigner.targetIntervals = this.targetIntervals
- realigner.scatterCount = this.scatterCount
-
- add(realigner)
- }
-}
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/external/sam-1.96.jar b/SequenceAnalysis/resources/external/sam-1.96.jar
deleted file mode 100644
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diff --git a/SequenceAnalysis/resources/external/tableToGraph.r b/SequenceAnalysis/resources/external/tableToGraph.r
deleted file mode 100644
index c16f6a40c..000000000
--- a/SequenceAnalysis/resources/external/tableToGraph.r
+++ /dev/null
@@ -1,53 +0,0 @@
-library(reshape)
-library(lattice)
-library(plyr)
-library(ggplot2)
-library(grid)
-library(perm)
-library(gridExtra)
-library(naturalsort)
-
-library(getopt);
-library(Matrix);
-
-spec <- matrix(c(
- 'inputFile', 'i', 1, "character",
- 'outputFile', 'o', 1, "character",
- 'plotTitle', 't', 2, "character",
- 'xLabel', NA, 2, "character",
- 'yLabel', NA, 2, "character",
- 'xColIdx', NA, 1, "integer",
- 'yColIdx', NA, 1, "integer",
- 'hasHeaders', 'h', 2, "logical"
-), ncol=4, byrow=TRUE);
-opts = getopt(spec, commandArgs(trailingOnly = TRUE));
-
-if ( is.null(opts$yLabel ) ) { opts$yLabel = "" }
-if ( is.null(opts$xLabel ) ) { opts$xLabel = "" }
-if ( is.null(opts$plotTitle ) ) { opts$plotTitle = "" }
-if ( is.null(opts$hasHeaders ) ) { opts$hasHeaders = TRUE }
-
-df <- read.table(opts$inputFile, quote="\"", header = opts$hasHeaders);
-
-xColName <-names(df)[opts$xColIdx];
-yColName <- names(df)[opts$yColIdx];
-#str(df)
-
-P<-ggplot(df,aes_string(x=xColName,y=yColName)) +
- ggtitle(opts$plotTitle) +
- #scale_y_continuous(limits=c(0,2),labels=c("0.0","0.5","1.0","1.5","2.0")) +
- geom_point(stat='identity') +
- theme(
- #axis.text.x = element_blank(),
- plot.margin = unit(c(0.3,0.3,0.3,0.3),"in"),
- plot.title = element_text(size=14,vjust=2),
- axis.title.x = element_text(size=14,vjust=-1),
- axis.title.y = element_text(size=14,vjust=2),
- strip.text.x = element_text(size = 12,face="bold")) +
- xlab(opts$xLabel) +
- ylab(opts$yLabel)
-
-
-png(opts$outputFile,width=880, height=680)
-print(P);
-dev.off();
\ No newline at end of file
diff --git a/SequenceAnalysis/resources/web/SequenceAnalysis/panel/VariantProcessingPanel.js b/SequenceAnalysis/resources/web/SequenceAnalysis/panel/VariantProcessingPanel.js
index 8f21bacc2..96436e527 100644
--- a/SequenceAnalysis/resources/web/SequenceAnalysis/panel/VariantProcessingPanel.js
+++ b/SequenceAnalysis/resources/web/SequenceAnalysis/panel/VariantProcessingPanel.js
@@ -249,7 +249,7 @@ Ext4.define('SequenceAnalysis.panel.VariantProcessingPanel', {
name: 'maxSamplesPerWorkspace',
label: 'Max Samples Per Workspace',
description: 'If multiple input gVCFs are provided, the pipeline will batch samples into workspaces with at most this many samples',
- defaultValue: 3000
+ defaultValue: 4000
},{
fieldXtype: 'ldk-integerfield',
name: 'batchSize',
diff --git a/SequenceAnalysis/src/org/labkey/sequenceanalysis/SequencePipelineServiceImpl.java b/SequenceAnalysis/src/org/labkey/sequenceanalysis/SequencePipelineServiceImpl.java
index f42aa99db..a8cb96339 100644
--- a/SequenceAnalysis/src/org/labkey/sequenceanalysis/SequencePipelineServiceImpl.java
+++ b/SequenceAnalysis/src/org/labkey/sequenceanalysis/SequencePipelineServiceImpl.java
@@ -523,6 +523,7 @@ public void registerResourceSettings(JobResourceSettings settings)
_resourceSettings.add(settings);
}
+ @Override
public Set getResourceSettings()
{
return _resourceSettings;
diff --git a/SequenceAnalysis/src/org/labkey/sequenceanalysis/run/util/FastqcRunner.java b/SequenceAnalysis/src/org/labkey/sequenceanalysis/run/util/FastqcRunner.java
index 8b11dea00..aadef9827 100644
--- a/SequenceAnalysis/src/org/labkey/sequenceanalysis/run/util/FastqcRunner.java
+++ b/SequenceAnalysis/src/org/labkey/sequenceanalysis/run/util/FastqcRunner.java
@@ -220,8 +220,8 @@ private String processOutput(List inputFiles, Set filesCreated, @Nul
return "";
}
- String output = "";
- String header = "
File Summary:
";
+ StringBuilder output = new StringBuilder();
+ StringBuilder header = new StringBuilder("