fls-bioinformatics-core / auto_process_ngs

Scripts and utilities for automatic processing & management of Illumina NGS sequencing data.
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Add options to trim reads in Fastq generation step #884

Closed pjbriggs closed 4 months ago

pjbriggs commented 10 months ago

Proposal to add options to the make_fastqs command to trim reads at the Fastq generation stage, as an alternative to explicitly setting the bases mask.

For example:

auto_process.py make_fastqs --read1=59 ...

would update the bases mask so that R1 would be trimmed to 59 bases (e.g. y59n...).