Releases: IARCbioinfo/needlestack
Releases · IARCbioinfo/needlestack
v1.1
Implemented enhancements:
- add needlestack logo in log.info #182
- add INFO field containing allelic frequency #174
- Add an option to only plot somatic mutations #149
- Make the main 3 processes pipe-friendly to avoid intermediate outputs #147
- Re-write pileup2baseindel.pl in C++ #146
- Flag possible cross-sample contamination of normal DNA in tumor samples #138
- Put ./. genotype when there is no power to identify a variant #137
- Implement Tumor-Normal pair somatic variant calling #133
- Add alignment plot in the PDF #73
- Make a script that would run needlestack without nextflow #72
Fixed bugs:
- max_dp default value in readme is wrong #176
- --help should exit 0 #161
- Manage bed specification for both bed and region #157
- Using renamed symlinks as input BAM files doesn't work with --use_file_name option #152
Closed issues:
v1.0
Implemented enhancements:
- Manage the three possible genotypes in vcf #130
- The graph showing AF vs log10(qval) should show phred-scaled qvalues #121
- Flag possible cross-sample contamination of normal DNA in tumor samples #138
- Put ./. genotype when there is no power to identify a variant #137
- Implement Tumor-Normal pair somatic variant calling #133
Fixed bugs:
- Contours seem to be incorrect #128
- correct file name extraction for sample name #126
- Let min_qval be equal to 0 #119
- plot improved error rate confidence interval #117
Closed issues:
v0.3
Implemented enhancements:
- Change the number of entry in the INFO and FORMAT VCF fields #108
- Add contour lines for a set of qvalues in the plot #100
- color points by qvalues in regression plot #85
- Add an option to choose output VCF file name (--out_vcf?) #81
- Add an option to directly input a region for calling in the command line #71
- Change the way we publish new version #69
- Make the stable docker file more stable #68
- Add more tests in CircleCI #55
- Remove unnecessary intermediate outputs #51
- Improve the bed split method #47
- In the absence of a bed file the pipeline should run on the full reference genome #39
- Add version numbers in VCF output #20
Fixed bugs:
- VCF files have to be sorted #110
- Sometimes large number in VCF files are written in scientific notations #109
- error when coverage is null for every bam file #99
- Calling doesn't work when a region contains only T in the reference #96
- Check that BAM folder contains bam files #66
- Check if the gzi is present if the ref is gz #65
- Verify the user inputs are correct #42
v0.2
New features
- Added
--no_indel
option (#56) - Added
--out_folder
option - The software is now called
needlestack
(#31) - Added program usage when launched with
--help
(#40) - Added information about the pipeline in the log (#41)
- We now verify the user inputs are correct (#42)
Improvements
- Added a zoomed regression plot (#21)
- Added contigs in VCF header (#25 and #34)
- Moved to IARCbioinfo organisation repo (#22)
- Corrected typos in readme, help and log (#53)
Changes
- Option
all_sites
is now a flag calledall_SNVs
and no longer needs to be set to TRUE or FALSE (#33) - Option
do_plots
is now a flag called--no_plots
and no longer needs to be set to TRUE or FALSE - Option
sample_names
is now a flag called--use_file_name
and no longer needs to be set to BAM or FILE
Bug fixes
- QVAL was wrongly called GQ for indels (#36)
- The pipeline no longer crashes if PDF files are not copied correctly (#49)