Releases: cancerit/alleleCount
Releases · cancerit/alleleCount
v4.2.1: htslib 1.11+libdeflate
- Correct htslib install for container
- add libdeflate via base container
- standardise install methods
v4.0.0 - fragment based counting
- alleleCounter now counts per-fragment rather than per-read when overlaps occur.
- When members of a pair overlap and calls match the depth and allele seen are only counted once.
- When mate reads disagree on the call, the depth is counted as 2 and both allele counts incremented.
- Reworked perl to wrap C alleleCounter and just handle the extra format changes.
- Removed dependency on Bio::DB::HTS.
- Update to HTSlib 1.7
- Merged #43, providing 10X processing mode.
v3.3.1
v3.2.2
Update htslib version to bring CGP stack in line
v3.1.1 - Dependancy correction
Fixes a missing dependancy only seen for those installing alleleCount without other elements of the cancerit stack.
v3.1.0 - Release gender integration
Minor release adding some functionality migrated from other projects into this more appropriate package.
v3.0.1 - htslib upgrade / legacy removal
- Removes dependancy on legacy versions of samtools in perl code.
- Upgrades to more recent version of htslib not requiring patch.
v2.2.0 - Added command line argument to filter on contig
- Added a contig filter commandline argument
V2.1.1 - bugfix release
Corrects failure to capture -q
option in alleleCounter.pl - please note the C version (alleleCounter
) is equivalent but much more efficient.
v2.1.0 Added htslib cram support with patch to htslib-1.2
Corrected bug in bam_access.c malloc where region wasn't allocated properly
Added patch to htslib-1.2 for full cram support (Resolves #9 )
Added version option to allelCounter c code commandline args