- For speedup in large number of samples, base counts are done on a per read group level, then merged into counts on larger partitions (samples, libraries, etc) + passed all integration tests before next item - Added additional summary item, a coverage threshold. Set by (possibly multiple) -ct flags, the summary outputs will have columns for "%_bases_covered_to_X"; both per sample, and per sample per interval summary files are effected (thus md5s changed for these) NOTE: This is the last revision that will include the per-gene summary files. Once DesignFileGenerator is sufficiently general, and has integration tests, it will be moved to core and the per-gene summary from Depth of Coverage will be retired. git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3437 348d0f76-0448-11de-a6fe-93d51630548a |
||
|---|---|---|
| .. | ||
| annotator | ||
| concordance | ||
| coverage | ||
| fasta | ||
| filters | ||
| genotyper | ||
| indels | ||
| qc | ||
| recalibration | ||
| sequenom | ||
| varianteval | ||
| PileupWalkerIntegrationTest.java | ||
| PrintReadsWalkerUnitTest.java | ||
| VariantsToVCFIntegrationTest.java | ||