Tools for working with genomic and high throughput sequencing data.
Group: FASTQ
Trims reads in one or more line-matched fastq files to a specific read length. The
individual fastq files are expected to have the same set of reads, as would be the
case with an r1.fastq
and r2.fastq
file for the same sample.
Optionally supports dropping of reads across all files when one or more reads is already shorter than the desired trim length.
Input and output fastq files may be gzipped.
Name | Flag | Type | Description | Required? | Max # of Values | Default Value(s) |
---|---|---|---|---|---|---|
input | i | PathToFastq | One or more input fastq files. | Required | Unlimited | |
output | o | PathToFastq | A matching number of output fastq files. | Required | Unlimited | |
length | l | Int | Length to trim reads to (either one per input fastq file, or one for all). | Required | Unlimited | |
exclude | x | Boolean | Exclude reads below the trim length. | Optional | 1 | false |