0.4.0 - Soft-clipping, YAML and more
-
SNPsplit now supports soft-clipping of reads (
CIGAR
operationS
). -
SNPsplit now writes important statistics out in YAML format to enable easier integration into
MultiQC
. Iftag2sort
is called viaSNPsplit
itself, the...sort.yaml
file will be integrated into the main...SNPsplit_report.yaml
file (and deleted afterwards) -
Added option
--skip_tag2sort
to allow the separation of the allele-tagging and allele-sorting (tag2sort
) processes. This might be desired to add a de-duplication step such asmarkduplicates
ordeduplicate_bismark
for Nextflow pipelines -
For genomes that consist of chromosomes for which SNPs are recorded, and scaffolds for which there are no SNPs, now all chromosomes and scaffolds are printed to both the N-masked and full sequence genomes (see here).
-
Added auto-detection of single-end or paired-end files. This avoids accidentally processing paired-end files in single-end mode see here.
-
Now making use of variable genome_build instead of using GRCm38 invariably