Version changelog

  • 4.1.0
    • Update minimap2 to version 2.26
    • SMRT Link v13.0 release
  • 4.0.0
    • Rename isoseq3 to isoseq
    • Add new tool isoseq cluster2
    • Update --max-5p-diff default value for isoseq collapse
    • Add X design option to isoseq tag to remove TSO sequences
  • 3.8.2
    • Update groupdedup to output consistent molecular IDs across runs
    • Bug fix updating rc and gp tags to passing for subset of correct reads
  • 3.8.1
    • Real-cell --method and --percentile options added to correct
  • 3.8.0
    • collapse allows isoforms with 5p degradation to collapse by default
    • --do-not-collapse-extra-5exons added to collapse
    • collapse max 5p and 3p distances can be set in CLI using --max-5p-diff and --max-3p-diff
    • Real-cell annotation in correct using rc tag
    • Real-cell filtering in groupdedup, dedup, and collapse
  • 3.7.0
    • Adding bcstats, correct, and groupdedup to CLI
    • bcstats emits frequency statistics for 10x barcodes
    • correct uses a truth-set to correct sequencing errors in cell barcodes
    • groupdedup provides substantial performance improvements over dedup
    • Support SEGMENT read type
  • 3.6.0
    • Adding tag and dedup to CLI
  • 3.5.0
    • SMRT Link release 11.0
    • Remove support for CLR data and disable polish step
    • Enable cluster --use-qvs as always on
  • 3.4.0
    • SMRT Link release 10.0.0
    • Add support for UMI and cell barcode handling, by adding tag and dedup
    • Add refine --min-rq to support RQ filtering for unfiltered <movie>.reads.bam input
  • 3.3.0
    • SMRT Link release 9.0.0
  • 3.2.2
    • Fix polish not generating fasta/q output. This bug was introduced in v3.2.0
  • 3.2.1
    • Fix a gff index 1-off bug in collapse
    • We have removed implicit dependencies from the bioconda recipe. Please install pbccs, lima, and pbcoretools as needed
  • 3.2.0
    • polish dropped support for RS II datasets!
    • Add collapse step for aligned transcript BAM input
    • Enable CCS-only workflow cluster --use-qvs
    • Add refine --min-polya-length
    • Add cluster --singletons to output unclustered FLNCs; potential sample prep artifacts!
    • Fix minimap2 bugs. Outputs might change slightly
  • 3.1.2
    • Reduce polish memory footprint
  • 3.1.1
    • Edge case fix where polish would not finish and stale
    • Improve polish run time for large scale datasets (> 1M CCS)
    • Improve polish result quality
  • 3.1.0
    • We outsourced the poly(A) tail removal and concatemer detection into a new tool called refine. Your custom primers.fasta is used in this step to detect concatemers

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