diff --git a/docs/build/html/.doctrees/environment.pickle b/docs/build/html/.doctrees/environment.pickle
index 0615eff..33ad2a2 100644
Binary files a/docs/build/html/.doctrees/environment.pickle and b/docs/build/html/.doctrees/environment.pickle differ
diff --git a/docs/build/html/.doctrees/index.doctree b/docs/build/html/.doctrees/index.doctree
index 6600a1f..e2047f1 100644
Binary files a/docs/build/html/.doctrees/index.doctree and b/docs/build/html/.doctrees/index.doctree differ
diff --git a/docs/build/html/.doctrees/installation.doctree b/docs/build/html/.doctrees/installation.doctree
index 7a0aada..c3f1542 100644
Binary files a/docs/build/html/.doctrees/installation.doctree and b/docs/build/html/.doctrees/installation.doctree differ
diff --git a/docs/build/html/.doctrees/usage.doctree b/docs/build/html/.doctrees/usage.doctree
index ae5fe15..f91e526 100644
Binary files a/docs/build/html/.doctrees/usage.doctree and b/docs/build/html/.doctrees/usage.doctree differ
diff --git a/docs/build/html/_sources/index.rst.txt b/docs/build/html/_sources/index.rst.txt
index 06b4c04..a7d27a3 100644
--- a/docs/build/html/_sources/index.rst.txt
+++ b/docs/build/html/_sources/index.rst.txt
@@ -8,11 +8,11 @@ What is SSAM-lite?
SSAM-lite is a lightweight, browser-based implementation of the `SSAM framework `__.
It provides the functionality of SSAMs most popular and widely used features in a graphical user interface
-with a few functions added for convenience and ease of use.
-
-
-TODO what does SSAM do
+with a few functions added for convenience and ease of use. It neiteher requires specialised computational experts
+nor hardware to handle and process data and thus can be run on a modest laptop.
+The SSAM framework allows for cell segmentation-free identification of cell-types by integrating prior knowledge of
+cell type-specific gene signatures with data from a variety of spatial in situ transcriptomics techniques.
Citations
=================
@@ -60,6 +60,5 @@ SOFTWARE.
quickstart
installation
- tutorial
usage
solo_vs_server
diff --git a/docs/build/html/_sources/installation.rst.txt b/docs/build/html/_sources/installation.rst.txt
index c1c0179..f60d27a 100644
--- a/docs/build/html/_sources/installation.rst.txt
+++ b/docs/build/html/_sources/installation.rst.txt
@@ -14,7 +14,7 @@ Supported Browsers
==================
TODO
-We should add some stuff about requirments etc
+We should add some stuff about requirements etc
SSAM-lite-solo
@@ -27,6 +27,7 @@ The installation of SSAM-lite-solo could not be easier. You either clone the
git clone https://github.com/sebastiantiesmeyer/ssamLite
+
or download it as zip-file from GitHub and then extract it.
That is literally all, you are ready to go.
@@ -45,6 +46,7 @@ To install SSAM-lite-server you first need to clone the
git clone https://github.com/sebastiantiesmeyer/ssamLiteDev
+
How to handle signatures ????
Download singatures: https://www.dropbox.com/s/8qxkgg16zelg6ya/new_sheet.tar.xz?dl=0
Place signatures in data/genetics/ ???
@@ -56,23 +58,30 @@ Next we create a ``conda`` environment (TODO we should provide a yaml?) and acti
conda create -n flask
conda activate flask
+
.. note::
You can set the environment name to your preferences.
+
Now we need to install some dependencies. TODO should we provide versions of the packages?
.. code-block:: bash
conda install flask numpy pandas
+
And start the server.
+
+.. code-block:: bash
+
cd /ssamLiteDev/scripts/flask
export FLASK_APP=run.py
export FLASK_ENV=development
flask run
-Open browser at 127.0.0.1:5000
+
+Type in the address bar of your browser: 127.0.0.1:5000
This definitely needs to be explained.
However, somebody with a little bit expertise should do this,
diff --git a/docs/build/html/_sources/usage.rst.txt b/docs/build/html/_sources/usage.rst.txt
index d9e2918..e565068 100644
--- a/docs/build/html/_sources/usage.rst.txt
+++ b/docs/build/html/_sources/usage.rst.txt
@@ -12,15 +12,15 @@ read :ref:`supported-browsers`. Connecting to SSAM-lite depends on whether you w
SSAM-lite-solo
--------------
-SSAM-lite-solo runs locally on your computer. It is executed by your Browser
-and to open it you onyl need to navigate to the unzipped SSAM-lite directory
-and double-click the *index.html* to open it in your default Web Browser.
+SSAM-lite-solo runs locally on your computer. It is executed by your browser
+and to open it you only need to navigate to the unzipped SSAM-lite directory
+and double-click the *index.html* and it will start in your default web browser.
SSAM-lite-server
----------------
-To connect to SSAM-lite-server, you will need to to open your favourite Web Browser (not IE)
-and enter the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000).
+To connect to SSAM-lite-server, you will need to to open your favourite web browser (not IE)
+and type the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000) into the address bar.
However, the IP and port depends on your local setup. Talk to your responsible SSAM-lite coordinator.
Navigation
@@ -36,76 +36,80 @@ by uploading your data.
Data
===========
-The Data will be uploaded in the **Data Center** section of the tool. By clicking the "Coordinates"
+The data will be uploaded in the **Data Center** section of the tool. By clicking the "Coordinates"
or "Signatures" button and selecting the correct files.
To be able to use SSAM-lite you need to prepare your data in csv format.
Two input files are required and must be structured as follows:
mRNA Coordinates
- This file needs to be of the form Gene, x-coordinate, y-coordinate.
+ This file needs to be of the form gene, x-coordinate, y-coordinate.
The name of the headers are irrelevant, however their order needs to be kept.
Negative coordinates are possible and the units do not matter. However, their magnitude
might have an influence on proper parameter values later on.
+----------+-----------+-----------+
- | Gene | x | y |
+ | gene, | x, | y |
+----------+-----------+-----------+
- | Gene A | 0.5 | 1.3 |
+ | gene A, | 0.5, | 1.3 |
+----------+-----------+-----------+
- | Gene A | 1.1 | 2.1 |
+ | gene A, | 1.1, | 2.1 |
+----------+-----------+-----------+
- | Gene B | 0.4 | 0.5 |
+ | gene B, | 0.4, | 0.5 |
+----------+-----------+-----------+
Gene Signatures
- This file should be a matrix of Cell types by Genes.
- The first column and row contains the names of Cell types and Genes, respectively. All the other cell values
+ This file should be a matrix of cell types by genes.
+ The first column and row contains the names of cell types and genes, respectively. All the other cell values
are gene scores ... TODO how to define this ...
This will later be used to assign each pixel to a cell type (or leave them unclassified)
- based on the Kernel Density Estimation.
+ based on the kernel density estimation.
+--------------+----------+-----------+-----------+
- | | Gene A | Gene B | Gene C |
+ | , | gene A, | gene B, | gene C |
+--------------+----------+-----------+-----------+
- | Celltype A | 0.5 | -0.5 | 1.3 |
+ | cell type A, | 0.5, | -0.5, | 1.3 |
+--------------+----------+-----------+-----------+
- | Celltype B | -0.2 | 1.1 | 2.1 |
+ | cell type B, | -0.2, | 1.1, | 2.1 |
+--------------+----------+-----------+-----------+
- | Celltype C | 0.3 | 0.4 | 0.5 |
+ | cell type C, | 0.3, | 0.4, | 0.5 |
+--------------+----------+-----------+-----------+
.. note::
- The name of the genes sre not relevant as there is no database used in the background.
+ The name of the genes need not be correct as there is no database used in the background.
But remember that the gene names from the coordinates and the signatures need to be the same
- (or at least the two sets of names must be at least partially overlapping).
+ (or more specifically the two sets of names must be partially overlapping).
Once both files are loaded you can proceed with setting the parameters for your analysis.
Parameters
===========
-For a deep understanding of the SSAM framework we would refer the user to the
+For a more detailed explanation of the SSAM framework we would refer the user to the
`SSAM publication `__,
however we will briefly describe the purpose and effect of the parameters
that can be set by the user to obtain optimal results.
Vector field width
The vector field width defines the horizontal pixel count of the output images.
- This is necessary as the KDE will be projected onto discrete locations (the pixels).
+ This is necessary as the kernel density estimation (KDE) will be projected onto
+ discrete locations (the pixels).
A higher value will result in higher resolution but also in increased processing time and memory
as well as size of the output images.
KDE kernel bandwidth (sigma)
- The kernel bandwidth TODO definition?
+ SSAM-lite uses a Gaussian kernel and the kernel bandwidth defines the "range" of
+ integration of data points (mRNA spots) for the KDE.
A higher value will result in an increased smoothing of the mRNA density estimation.
Cell assignment threshold
This threshold is used to decide whether a pixel in the KDE projection belongs to
- a cell or not. It is visualised in the parameter preview to help find an
- optimal value.
+ a cell or not.
+
+ As help to pick an optimal value you can check the KDE estimate (middle plot in the parameter preview)
+ to find the intensity that should serve as cutoff point.
Each of the parameters can be set in their respective field and applied by hitting Enter.
@@ -129,7 +133,7 @@ Once it finished, the KDE estimates will be displayed in a plot (see example bel
This step is the computationally most expensive and might tak a few minutes.
.. note::
- If you are using SSAM-lite-solo your Browser might warn you that it is being slowed down by the current site.
+ If you are using SSAM-lite-solo your browser might warn you that it is being slowed down by the current site.
This is normal due to the heavy computation running in the background and can be ignored.
.. image:: ../res/imgs/KDE.png
@@ -144,7 +148,7 @@ The inferred cell types will be displayed in a new plot.
:width: 800
:alt: Cell types inferred from KDE using the provided gene signatures
-If you are not content with the results you can go back to the parameters section
+If you are not satisfied with the results you can go back to the parameters section
and refine those before rerunning the analysis.
@@ -153,4 +157,4 @@ Save results
All plots are produced with `Plotly `__ and can be downloaded
by hovering over the plot which triggers a legend to appear in the upper right corner,
-now click the Camera icon which lets you download the current plot as png file.
+now click the camera icon which lets you download the current plot as png file.
diff --git a/docs/build/html/genindex.html b/docs/build/html/genindex.html
index 657f330..9572026 100644
--- a/docs/build/html/genindex.html
+++ b/docs/build/html/genindex.html
@@ -38,7 +38,6 @@
SSAM-lite is a lightweight, browser-based implementation of the SSAM framework.
It provides the functionality of SSAMs most popular and widely used features in a graphical user interface
-with a few functions added for convenience and ease of use.
-
TODO what does SSAM do
+with a few functions added for convenience and ease of use. It neiteher requires specialised computational experts
+nor hardware to handle and process data and thus can be run on a modest laptop.
+
The SSAM framework allows for cell segmentation-free identification of cell-types by integrating prior knowledge of
+cell type-specific gene signatures with data from a variety of spatial in situ transcriptomics techniques.
SSAM-lite-server Previous
- Next
+ Next
diff --git a/docs/build/html/objects.inv b/docs/build/html/objects.inv
index c3248bb..aff2de0 100644
--- a/docs/build/html/objects.inv
+++ b/docs/build/html/objects.inv
@@ -2,6 +2,5 @@
# Project: SSAM-lite
# Version:
# The remainder of this file is compressed using zlib.
-xڅ1o w~RҪk:DV#bz9Ǒ6lHݎ=Dg7#=5e7=AQ,1m
-^t^6Vcq@á}~Q͝>EFfhةY.:}
-
˚"$ o5}0khӝΖ0۟>{Wa%JxKR7NMtG$Fcn>%5:1#9
Yˋߧ>]HW4
\ No newline at end of file
+xڅ1O0w`5R1Vn|J,\]
+uش=n,ٛzOC/GoiTkRBE7i^;M8jjdoz12%;y?,}S_k?c eUdz6(Fھ>L4ߙ'MA3?L'gCU$uTMOHACէ3&)o_|="r
\ No newline at end of file
diff --git a/docs/build/html/search.html b/docs/build/html/search.html
index 35610d0..01e05bf 100644
--- a/docs/build/html/search.html
+++ b/docs/build/html/search.html
@@ -41,7 +41,6 @@
SSAM-lite-solo runs locally on your computer. It is executed by your Browser
-and to open it you onyl need to navigate to the unzipped SSAM-lite directory
-and double-click the index.html to open it in your default Web Browser.
+
SSAM-lite-solo runs locally on your computer. It is executed by your browser
+and to open it you only need to navigate to the unzipped SSAM-lite directory
+and double-click the index.html and it will start in your default web browser.
To connect to SSAM-lite-server, you will need to to open your favourite Web Browser (not IE)
-and enter the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000).
+
To connect to SSAM-lite-server, you will need to to open your favourite web browser (not IE)
+and type the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000) into the address bar.
However, the IP and port depends on your local setup. Talk to your responsible SSAM-lite coordinator.
The Data will be uploaded in the Data Center section of the tool. By clicking the “Coordinates”
+
The data will be uploaded in the Data Center section of the tool. By clicking the “Coordinates”
or “Signatures” button and selecting the correct files.
To be able to use SSAM-lite you need to prepare your data in csv format.
Two input files are required and must be structured as follows:
-
mRNA Coordinates
This file needs to be of the form Gene, x-coordinate, y-coordinate.
+
mRNA Coordinates
This file needs to be of the form gene, x-coordinate, y-coordinate.
The name of the headers are irrelevant, however their order needs to be kept.
Negative coordinates are possible and the units do not matter. However, their magnitude
might have an influence on proper parameter values later on.
This file should be a matrix of Cell types by Genes.
-The first column and row contains the names of Cell types and Genes, respectively. All the other cell values
+
Gene Signatures
This file should be a matrix of cell types by genes.
+The first column and row contains the names of cell types and genes, respectively. All the other cell values
are gene scores … TODO how to define this …
This will later be used to assign each pixel to a cell type (or leave them unclassified)
-based on the Kernel Density Estimation.
For a deep understanding of the SSAM framework we would refer the user to the
+
For a more detailed explanation of the SSAM framework we would refer the user to the
SSAM publication,
however we will briefly describe the purpose and effect of the parameters
that can be set by the user to obtain optimal results.
Vector field width
The vector field width defines the horizontal pixel count of the output images.
-This is necessary as the KDE will be projected onto discrete locations (the pixels).
+This is necessary as the kernel density estimation (KDE) will be projected onto
+discrete locations (the pixels).
A higher value will result in higher resolution but also in increased processing time and memory
as well as size of the output images.
-
KDE kernel bandwidth (sigma)
The kernel bandwidth TODO definition?
+
KDE kernel bandwidth (sigma)
SSAM-lite uses a Gaussian kernel and the kernel bandwidth defines the “range” of
+integration of data points (mRNA spots) for the KDE.
A higher value will result in an increased smoothing of the mRNA density estimation.
Cell assignment threshold
This threshold is used to decide whether a pixel in the KDE projection belongs to
-a cell or not. It is visualised in the parameter preview to help find an
-optimal value.
+a cell or not.
+
As help to pick an optimal value you can check the KDE estimate (middle plot in the parameter preview)
+to find the intensity that should serve as cutoff point.
Each of the parameters can be set in their respective field and applied by hitting Enter.
@@ -226,7 +228,7 @@
All plots are produced with Plotly and can be downloaded
by hovering over the plot which triggers a legend to appear in the upper right corner,
-now click the Camera icon which lets you download the current plot as png file.
+now click the camera icon which lets you download the current plot as png file.
@@ -249,7 +251,7 @@
Save results
- Previous
+ PreviousNext
diff --git a/docs/source/index.rst b/docs/source/index.rst
index 06b4c04..a7d27a3 100644
--- a/docs/source/index.rst
+++ b/docs/source/index.rst
@@ -8,11 +8,11 @@ What is SSAM-lite?
SSAM-lite is a lightweight, browser-based implementation of the `SSAM framework `__.
It provides the functionality of SSAMs most popular and widely used features in a graphical user interface
-with a few functions added for convenience and ease of use.
-
-
-TODO what does SSAM do
+with a few functions added for convenience and ease of use. It neiteher requires specialised computational experts
+nor hardware to handle and process data and thus can be run on a modest laptop.
+The SSAM framework allows for cell segmentation-free identification of cell-types by integrating prior knowledge of
+cell type-specific gene signatures with data from a variety of spatial in situ transcriptomics techniques.
Citations
=================
@@ -60,6 +60,5 @@ SOFTWARE.
quickstart
installation
- tutorial
usage
solo_vs_server
diff --git a/docs/source/installation.rst b/docs/source/installation.rst
index c1c0179..f60d27a 100644
--- a/docs/source/installation.rst
+++ b/docs/source/installation.rst
@@ -14,7 +14,7 @@ Supported Browsers
==================
TODO
-We should add some stuff about requirments etc
+We should add some stuff about requirements etc
SSAM-lite-solo
@@ -27,6 +27,7 @@ The installation of SSAM-lite-solo could not be easier. You either clone the
git clone https://github.com/sebastiantiesmeyer/ssamLite
+
or download it as zip-file from GitHub and then extract it.
That is literally all, you are ready to go.
@@ -45,6 +46,7 @@ To install SSAM-lite-server you first need to clone the
git clone https://github.com/sebastiantiesmeyer/ssamLiteDev
+
How to handle signatures ????
Download singatures: https://www.dropbox.com/s/8qxkgg16zelg6ya/new_sheet.tar.xz?dl=0
Place signatures in data/genetics/ ???
@@ -56,23 +58,30 @@ Next we create a ``conda`` environment (TODO we should provide a yaml?) and acti
conda create -n flask
conda activate flask
+
.. note::
You can set the environment name to your preferences.
+
Now we need to install some dependencies. TODO should we provide versions of the packages?
.. code-block:: bash
conda install flask numpy pandas
+
And start the server.
+
+.. code-block:: bash
+
cd /ssamLiteDev/scripts/flask
export FLASK_APP=run.py
export FLASK_ENV=development
flask run
-Open browser at 127.0.0.1:5000
+
+Type in the address bar of your browser: 127.0.0.1:5000
This definitely needs to be explained.
However, somebody with a little bit expertise should do this,
diff --git a/docs/source/quickstart.rst b/docs/source/quickstart.rst
index 876f199..8668928 100644
--- a/docs/source/quickstart.rst
+++ b/docs/source/quickstart.rst
@@ -20,7 +20,12 @@ to download SSAM-lite-solo as zip, and extract it.
Test data
=========
-Download the test data from ..... TODO
+Download the test data from Zenodo via
+
+.. code-block:: bash
+
+ wget https://zenodo.org/record/ .... TODO
+
My first analysis
diff --git a/docs/source/tutorial.rst b/docs/source/tutorial.rst
deleted file mode 100644
index fa61da1..0000000
--- a/docs/source/tutorial.rst
+++ /dev/null
@@ -1,10 +0,0 @@
-########
-Tutorial
-########
-
-
-TODO do we need a tutorial? there is not a lot of room between the quickstart and the usage anyway?
-
-After installation of SSAM-lite, this tutorial will help you get to
-know the basic workflow of
-
diff --git a/docs/source/usage.rst b/docs/source/usage.rst
index d9e2918..f919c77 100644
--- a/docs/source/usage.rst
+++ b/docs/source/usage.rst
@@ -2,6 +2,9 @@
Usage
####################
+If you want to follow our usage guide along with some sample data you can download a sample data set from
+Zenodo (https://zenodo.org/doi????).
+
Open SSAM-lite
==============
@@ -12,15 +15,15 @@ read :ref:`supported-browsers`. Connecting to SSAM-lite depends on whether you w
SSAM-lite-solo
--------------
-SSAM-lite-solo runs locally on your computer. It is executed by your Browser
-and to open it you onyl need to navigate to the unzipped SSAM-lite directory
-and double-click the *index.html* to open it in your default Web Browser.
+SSAM-lite-solo runs locally on your computer. It is executed by your browser
+and to open it you only need to navigate to the unzipped SSAM-lite directory
+and double-click the *index.html* and it will start in your default web browser.
SSAM-lite-server
----------------
-To connect to SSAM-lite-server, you will need to to open your favourite Web Browser (not IE)
-and enter the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000).
+To connect to SSAM-lite-server, you will need to to open your favourite web browser (not IE)
+and type the correct IP address and port in the form {ip}:{port} (e.g. 127.0.0.1:5000) into the address bar.
However, the IP and port depends on your local setup. Talk to your responsible SSAM-lite coordinator.
Navigation
@@ -36,76 +39,80 @@ by uploading your data.
Data
===========
-The Data will be uploaded in the **Data Center** section of the tool. By clicking the "Coordinates"
+The data will be uploaded in the **Data Center** section of the tool. By clicking the "Coordinates"
or "Signatures" button and selecting the correct files.
To be able to use SSAM-lite you need to prepare your data in csv format.
Two input files are required and must be structured as follows:
mRNA Coordinates
- This file needs to be of the form Gene, x-coordinate, y-coordinate.
+ This file needs to be of the form gene, x-coordinate, y-coordinate.
The name of the headers are irrelevant, however their order needs to be kept.
Negative coordinates are possible and the units do not matter. However, their magnitude
might have an influence on proper parameter values later on.
+----------+-----------+-----------+
- | Gene | x | y |
+ | gene, | x, | y |
+----------+-----------+-----------+
- | Gene A | 0.5 | 1.3 |
+ | gene A, | 0.5, | 1.3 |
+----------+-----------+-----------+
- | Gene A | 1.1 | 2.1 |
+ | gene A, | 1.1, | 2.1 |
+----------+-----------+-----------+
- | Gene B | 0.4 | 0.5 |
+ | gene B, | 0.4, | 0.5 |
+----------+-----------+-----------+
Gene Signatures
- This file should be a matrix of Cell types by Genes.
- The first column and row contains the names of Cell types and Genes, respectively. All the other cell values
+ This file should be a matrix of cell types by genes.
+ The first column and row contains the names of cell types and genes, respectively. All the other cell values
are gene scores ... TODO how to define this ...
This will later be used to assign each pixel to a cell type (or leave them unclassified)
- based on the Kernel Density Estimation.
+ based on the kernel density estimation.
+--------------+----------+-----------+-----------+
- | | Gene A | Gene B | Gene C |
+ | , | gene A, | gene B, | gene C |
+--------------+----------+-----------+-----------+
- | Celltype A | 0.5 | -0.5 | 1.3 |
+ | cell type A, | 0.5, | -0.5, | 1.3 |
+--------------+----------+-----------+-----------+
- | Celltype B | -0.2 | 1.1 | 2.1 |
+ | cell type B, | -0.2, | 1.1, | 2.1 |
+--------------+----------+-----------+-----------+
- | Celltype C | 0.3 | 0.4 | 0.5 |
+ | cell type C, | 0.3, | 0.4, | 0.5 |
+--------------+----------+-----------+-----------+
.. note::
- The name of the genes sre not relevant as there is no database used in the background.
+ The name of the genes need not be correct as there is no database used in the background.
But remember that the gene names from the coordinates and the signatures need to be the same
- (or at least the two sets of names must be at least partially overlapping).
+ (or more specifically the two sets of names must be partially overlapping).
Once both files are loaded you can proceed with setting the parameters for your analysis.
Parameters
===========
-For a deep understanding of the SSAM framework we would refer the user to the
+For a more detailed explanation of the SSAM framework we would refer the user to the
`SSAM publication `__,
however we will briefly describe the purpose and effect of the parameters
that can be set by the user to obtain optimal results.
Vector field width
The vector field width defines the horizontal pixel count of the output images.
- This is necessary as the KDE will be projected onto discrete locations (the pixels).
+ This is necessary as the kernel density estimation (KDE) will be projected onto
+ discrete locations (the pixels).
A higher value will result in higher resolution but also in increased processing time and memory
as well as size of the output images.
KDE kernel bandwidth (sigma)
- The kernel bandwidth TODO definition?
+ SSAM-lite uses a Gaussian kernel and the kernel bandwidth defines the "range" of
+ integration of data points (mRNA spots) for the KDE.
A higher value will result in an increased smoothing of the mRNA density estimation.
Cell assignment threshold
This threshold is used to decide whether a pixel in the KDE projection belongs to
- a cell or not. It is visualised in the parameter preview to help find an
- optimal value.
+ a cell or not.
+
+ As help to pick an optimal value you can check the KDE estimate (middle plot in the parameter preview)
+ to find the intensity that should serve as cutoff point.
Each of the parameters can be set in their respective field and applied by hitting Enter.
@@ -129,7 +136,7 @@ Once it finished, the KDE estimates will be displayed in a plot (see example bel
This step is the computationally most expensive and might tak a few minutes.
.. note::
- If you are using SSAM-lite-solo your Browser might warn you that it is being slowed down by the current site.
+ If you are using SSAM-lite-solo your browser might warn you that it is being slowed down by the current site.
This is normal due to the heavy computation running in the background and can be ignored.
.. image:: ../res/imgs/KDE.png
@@ -144,7 +151,7 @@ The inferred cell types will be displayed in a new plot.
:width: 800
:alt: Cell types inferred from KDE using the provided gene signatures
-If you are not content with the results you can go back to the parameters section
+If you are not satisfied with the results you can go back to the parameters section
and refine those before rerunning the analysis.
@@ -153,4 +160,4 @@ Save results
All plots are produced with `Plotly `__ and can be downloaded
by hovering over the plot which triggers a legend to appear in the upper right corner,
-now click the Camera icon which lets you download the current plot as png file.
+now click the camera icon which lets you download the current plot as png file.