gatk-3.8/java/src/org/broadinstitute/sting
asivache 3208eaabcc A standalone picard-level tool for breaking individual reads into "pairs" of first/last N bases. Supports:
* splitting off only start or end of the read, or both; the output will contain 
     chopped sequences AND corresponding base qualities
   * splitting arbitrary number of bases off each end (different numbers
     for left and right segments can be specified; segments can overlap)
   * splitting only unmapped reads, ignoring mapped ones
   * writing splitted ends into separate sam/bam files, or into a single output file
   * decorating original read names with user-specified suffixes for each end
     (e.g. _1 and _2 for left and right parts of the read); default: no decoration, 
     original read names are used
   *  when mapped reads are split, the alignment cigars are chopped appropriately
     and the alignment start positions are adjusted (for the right end) to correctly 
    specify the alignment of the selected part of the read


git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@1402 348d0f76-0448-11de-a6fe-93d51630548a
2009-08-10 20:42:49 +00:00
..
gatk warn user when dbSNP rod looks suspicious 2009-08-10 20:20:20 +00:00
playground A standalone picard-level tool for breaking individual reads into "pairs" of first/last N bases. Supports: 2009-08-10 20:42:49 +00:00
secondarybase Cleanup...deprecate FastaSequenceFile2 in favor of IndexedFastaSequenceFile or ReferenceSequenceFile from Picard, depending on the application. 2009-07-08 18:49:08 +00:00
utils Continuing cleanup of SSG. GenotypeLikelihoods now have extensive testing routines. DiploidGenotype supports het, homref, etc calculations. SSG has been cleaned up to remove old garbage functionality. Also now supports output to standard output by simply omitting varout 2009-08-05 22:25:30 +00:00