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Mergepair vsearch

Yoann Dufresne edited this page Dec 13, 2018 · 3 revisions

This module give you the possibility to get the assembly of the forward and reverse reads.
For space efficiency, the reads are dereplicated after the merging process. A size value is added in each read header to keep the abundance.

Module interactions

Main inputs

  • Forward reads: The FASTQ file containing the forward reads.
  • Reverse reads: The FASTQ file containing the reverse reads.
  • Output file: The FASTA file within the assembled reads will be outputted.

Options

  • Quality extremum: The limit quality thresholds. If a nucleotide is over the max or under the min the sequence will be rejected.
  • Merged read size extremum: Minimum and maximum length for assembled read.
  • Read maximum differences: Maximum mismatches in the forward/reverse overlap.
  • Read minimum overlap: Minimum length of the forward/reverse overlap.

References

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