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Releases: BLinkseq/djinn
Releases · BLinkseq/djinn
Release list
2.5
2.4
2.3
New
- add
fastq count - add
sam count
Both of which write barcode<tab>count to stdout
2.2.1
Fix
fastq standardizewas not outputting barcodes when--stylewasn't provided-- it does now!!
2.2
2.1.1
2.1
New
- migrate
assign-mifrom harpy todjinn sam- assigns
MIandBXtags for unique molecules based on an alignment distance threshold
- assigns
- migrate
concatfrom harpy todjinn sam- concatenate SAM/BAM files while preserving within-sample molecule uniqueness
djinn samcommands have a-S/--samoption to output SAM format instead of BAM- specify where interleaved files wont work
Fixes
- fixed
sam standardizeincorrectly outputting only the first occurrence of a new barcode when-sstyle was invoked
Full Changelog: 2.0...2.1
2.0
Changes
- commands now need to prefixed with
samorfastqdepending on the type of input file fastqcommands accept one single-end or two paired-end filesfastqcommands have--threadsoption to using systempigz(if available) to speed up writing- better fastq singleton filtering that accounts for the source of a barcode being one single-end or two paired-end reads
downsamplerenamedsample
Full Changelog: 1.1...2.0
1.1
New
filter-singletonsto remove reads with singleton barcodesfilter-invalidto remove invalid barcodes- fastq file writing has been replaced with a fancy new internal cache object that can be configured with the hidden option
--cache-sizeto help control gzip output speed- this also means no more writing uncompressed fastq and compressing after-- all fastq output is gzipped-on-write
1.0.1
Bugs fixed
- [hic-spoof] ignore invalid reads (they are moved as-is into output, no spoofing is done with them)
- [hic-spoof] fix first read in barcode pool not being added to said pool