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v0.2.0

  • add duphold annotations. (requires duphold v0.0.4)

v0.1.11

  • flip start and end for small percent of cases where that's a problem
  • expose min sample weight to allow adjusting required support for each variant

v0.1.10

  • fix type in annotate (s/Number/Integer/)

v0.1.9

  • better error message in merge.
  • use set -e in process calls so we don't exit with 0 even on failure

v0.1.8

  • don't use --sum in merge step. this reduces the size of CI when using smoove merge

v0.1.7

  • add a SHQ: smoove het-quality score to the FORMAT field and a MSHQ:mean smoove het-quality score to the INFO. Variants with a het-quality of 4 are quite good.

v0.1.6

  • sensitivity improvement by dropping reads with > 5 mismatches.

v0.1.5

  • sensitivity increases for variants without split reads.
  • use a fixed length of 4 in merge (gives much better merging)
  • add new annotate command which takes a gff and annotates with gene names
  • increase max_reads argument to svtyper to reduce false negatives
  • remove QCFail and duplicate reads from split and disc.bams. This is now part of smoove but also fixed in lumpy_filter upstream.

v0.1.4

  • fix bug when using -x/--removepr with --genotype (thanks @brad for test-case)

v0.1.3

  • update command to match latest mosdepth

v0.1.2

  • bcftools and gsort are now required.
  • output never goes to STDOUT
  • output contigs to header
  • add svtools to docker
  • add option to remove PRPOS and PREND