Releases: genome/cle-myeloseqhd
Releases · genome/cle-myeloseqhd
dragen v4.2.4
Replace RIS local docker registry images and fix a bug of filtering variants
- Replace all RIS local docker registry images
- Fix a bug of filtering variants that exist in prior cases but get ALT read count lower than threshold
- Remove unneeded remove_rundir task and several redundant variables in workflow, set GenotypeVcf in analysis sub workflow
- Update launcher.pl with new sample naming and X_Plus info_string
Fix a multiallelic site bug and change QC coverage threshold
- Add "-m none" to bcftools merge command line to fix multlallelic variants
- Lower average target alignment coverage from 4000 to 2500, Change metrics target bases > 2000x to > 1250x
- Update launcher script and script paths in workflow.
Use dragen 4.0.3, demux setting change, remove strand bias filter, and other updates
- Use dragen version 4.0.3
- Change dragen demux setting to trim 1 base from 5' and 2 bases from 3'
- Remove StrandBias filter
- Add "--qc-coverage-ignore-overlaps true" to dragen align command
- Add "-F x" to the bcftools merge command of MyeloseqHDAnalysis.wdl to preserves 'PASS' filter if one of the merged files has 'PASS'
- Several updates for filterHaloplex.py (refer to https://jira.wustl.edu/browse/CI-934)
- application.conf and WDL workflow updates to be compatible for dragen-3 and dragen-4
Update Coverage Bed and launcher.pl
- Update coverage bed with different BRAF ensembl transcript ID and exon_15
- Update launcher.pl to better handle exception columns and positive control samples.
Improve UMI collapsing, Add QC review status and others
- Update dragen align command to correctly handle UMI collapse
- Add QC review status, change several QC metrics thresholds and report these metrics accordingly
- Check small demux_fastq size as sign of potential wrong index and stop the workflow
- Make launcher.pl to use Illumina run folder and align input files on storage1 as dragen demux/align command inputs
- Make launcher.pl to handle special cases of RESEQ, RESEARCH, NOTRANSFER properly
- Remove unneeded output files from data_transfer
Drop freebayes, Update variant filtering, Include prior MRNs for DB querying
- Remove freebayes from variant calling
- Update filterHaloplex.py for better variant filtering
- Include prior MRNs for query_DB task
Refer to https://jira.wustl.edu/browse/CI-779
Initial Release
This is the initial release of MyeloseqHD analysis wdl workflow.