Fix vcf header bug: T/N SAMPLE lines are back - needed for import to SolveBio add strandedness: auto for -l A option in salmon report 10x more peaks in CHIP/ATAC-seq - use 0.05 qvalue fix misleading RNA-seq duplicated reads statistics: thanks @sib-bcf reorganize conda environments snpEff 5.0 strandedness: auto document WGBS pipeline steps make --local an option, not default in bismark alignment - too slow bcbioRNASeq update to 0.3.44 pureCN update to 2.0.1 octopus update to 0.7.
Import shared dependency functions from bcbioBase instead of basejump. Added method support for sele...
Fixed a bug in the vcf2hdf5_parallel script (#58 - @travc). Fixed a bug relating to the is_snp field...
[3.7] - 2022-05-03 :warning: Major enhancements Updated default STAR version to latest available (2...
1.2.4 (21 September 2020) Remove deprecated --genomicsdb-use-vcf-codec option as this is now the de...
1.2.5 (01 January 2021) Joint calling for RNA-seq variant calling requires setting jointcaller to b...
Set ENCODE library complexity flags properly for ChIP-seq. Thanks to @mistrm82. Fix greylisted peaks...
Fix for get VEP cache. Support Picard's new syntax for ReorderSam (REFERENCE -> SEQUENCE_DICTIONARY)...
Fix for bismark not being a supported aligner. Run ataqv (https://github.com/ParkerLab/ataqv) to cal...
Update ChIP and ATAC bowtie2 runs to use --very-sensitive. Properly pad TSS BED file for ataqv TSS e...
RNASeq: Add gene body coverage plots to multiqc report. Restore ability to opt out of contamination...
[3.10] - 2022-12-21 Enhancements & fixes Bump minimum Nextflow version from 21.10.3 -> 22.10.1 Upda...
RNASeq: Fail more gracefully if SummarizedExperiment object cannot be created. Fixes to handle DRAGE...
general changes work around a bug in ntcard (fixes #43) bypass non-ACGTU characters in input reads ...
[3.1] - 2021-05-13 :warning: Major enhancements Samplesheet format has changed from group,replicate...
Provide initial support for nanopore RNA-seq data (cDNA/direct RNA). See README for example usage fo...
Import shared dependency functions from bcbioBase instead of basejump. Added method support for sele...
Fixed a bug in the vcf2hdf5_parallel script (#58 - @travc). Fixed a bug relating to the is_snp field...
[3.7] - 2022-05-03 :warning: Major enhancements Updated default STAR version to latest available (2...
1.2.4 (21 September 2020) Remove deprecated --genomicsdb-use-vcf-codec option as this is now the de...
1.2.5 (01 January 2021) Joint calling for RNA-seq variant calling requires setting jointcaller to b...
Set ENCODE library complexity flags properly for ChIP-seq. Thanks to @mistrm82. Fix greylisted peaks...
Fix for get VEP cache. Support Picard's new syntax for ReorderSam (REFERENCE -> SEQUENCE_DICTIONARY)...
Fix for bismark not being a supported aligner. Run ataqv (https://github.com/ParkerLab/ataqv) to cal...
Update ChIP and ATAC bowtie2 runs to use --very-sensitive. Properly pad TSS BED file for ataqv TSS e...
RNASeq: Add gene body coverage plots to multiqc report. Restore ability to opt out of contamination...
[3.10] - 2022-12-21 Enhancements & fixes Bump minimum Nextflow version from 21.10.3 -> 22.10.1 Upda...
RNASeq: Fail more gracefully if SummarizedExperiment object cannot be created. Fixes to handle DRAGE...
general changes work around a bug in ntcard (fixes #43) bypass non-ACGTU characters in input reads ...
[3.1] - 2021-05-13 :warning: Major enhancements Samplesheet format has changed from group,replicate...
Provide initial support for nanopore RNA-seq data (cDNA/direct RNA). See README for example usage fo...
Import shared dependency functions from bcbioBase instead of basejump. Added method support for sele...
Fixed a bug in the vcf2hdf5_parallel script (#58 - @travc). Fixed a bug relating to the is_snp field...
[3.7] - 2022-05-03 :warning: Major enhancements Updated default STAR version to latest available (2...