This is a test version of Biostars. For the public version, visit https://www.biostars.org.
how to parse raw reads to unique reads with count for fast alignment

i want to parse raw reads to unique reads with count for fast alignment for use in mirdp. suggest some pipelines except mapper.pl

next-gen rna-seq

Hi manishbiotechie,

This question needs more information. Please elaborate on which data you have and what you aim to achieve.

Regards,
Wouter

1 answer

see FASTQ/A Collapser

Collapsing identical sequences in a FASTQ/A file into a single sequence (while maintaining reads counts)

Log in to answer this question.