1.0.0
Pre-release
Pre-release
GRIDSS 1.0.0 is available and is now truly a software suite with each step now a separate, independent tool.
- Explicit support for (bowtie2-style) multi-mapping reads.
- New set of command-line tools in the gridss namespace:
- CallVariants (this replaces Idsv as the all-in-one wrapper tool)
- CollectGridssMetrics
- CollectCigarMetrics
- CollectIdsvMetrics
- CollectMapqMetrics
- ExtractSVReads
- ComputeSamTags
- SoftClipsToSplitReads
- IdentifyVariants
- AnnotateVariants
- AllocateEvidence
- AnnotateReferenceCoverage
- AnnotateInexactHomology
- Intermediate files now use the standard SAM tags and are much more useful for variant visualisation
- Improved parallelisation
- Parallelisation is no longer per chromosome and is now performed of arbitrarily sized genomic intervals (1Mb by default)
- Variant identifiers are now deterministic
- Split read handling is now symmetrical (no more RSR in the output file)
- Assemblies still track the breakend from from which the contig was assembled
- Indel-containing reads are now tracked separately to split reads
- Improved support for single-end sequencing
Be sure to check out the README file and the updated examples for the new command line syntax.