Releases
0.3.0
New features
freebayes variant calling
naibr variant calling
bam filename/RG tag validations
unit testing (not relevant for end-user)
--vcf-samples
options for impute
and phase
file/vcf sample validations
STITCH parameter file validations
genome assembly bgzipping validation/handling
much more flexible regex for fastq filenames
STITCH param file column order no longer matters and is not case-sensitive
new demultiplex
module for Generation I (Meier et al., 2022) haplotag beads
Breaking changes
snp and sv variant calling now split into separate submodules under variants
variants --method
is now variants snp --method
and variants sv --method
STITCH param file has extra column bxlimit
the validations listed above will force Harpy to terminate if errors are detected
folder structure for output of align
slightly different
Non-breaking changes
added Snakemake --nolock
and --rerun-incomplete
flags to all workflows
all workflows now provide appropriate exit codes
snp variant calling now occurs by genomic interval rather than by contig (a lot more parallel, a lot faster)
EMA aligns all preproc files at once into single alignment file, rather than aligning each individually and merging after
samtools stats/flagstat reports combined into single report
phase
reports reworked/rewritten
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