NAME

fromsam

USAGE

Usage: recs fromsam <args> [<files>]
   Each line of input (or lines of <files>) is parsed as a SAM (Sequence
   Alignment/Map) formatted record to produce a recs output record. To parse a
   BAM file, please pipe it from `samtools view file.bam` into this command.

   The output records will contain the following fields:

      qname flag rname pos mapq cigar rnext pnext tlen seq qual

   Additional optional SAM fields are parsed into the "tag" key, which is a hash
   keyed by the SAM field tag name. The values are also hashes containing a
   "type" and "value" field. For example, a read group tag will end up in your
   record like this:

      tags => {
        RG => {
          type  => "Z",
          value => "...",
        }
      }

   Refer to the SAM spec for field details: http://samtools.github.io/hts-
   specs/SAMv1.pdf

Arguments:
   --flags                      Decode flag bitstring into a "flags" hashref
   --quals                      Decode qual string into a "quals" array of
                                numeric values
   --filename-key|fk <keyspec>  Add a key with the source filename (if no
                                filename is applicable will put NONE)

  Help Options:
      --help  This help screen

Examples:
   Parse SAM and calculate average mapping quality:
      recs fromsam input.sam | recs collate -a avg,mapq
   Parse BAM:
      samtools view input.bam | recs fromsam
   Parse SAM pre-filtered by read group:
      samtools view -r SAMPLE-1234 input.sam | recs fromsam
   The same, but probably slower:
      recs fromsam input.sam | recs grep '{{tag/RG/value}} eq "SAMPLE-1234"'

SEE ALSO

App::RecordStream::Bio