nanofilt | Filtering and trimming of long read sequencing data | Genomics library
kandi X-RAY | nanofilt Summary
kandi X-RAY | nanofilt Summary
Filtering and trimming of long read sequencing data. Filtering on quality and/or read length, and optional trimming after passing filters. Reads from stdin, writes to stdout. Optionally reads directly from an uncompressed file specified on the command line.
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Top functions reviewed by kandi - BETA
- Filter fastq files based on summary
- Calculate the average quality of a sequence
- Argument parser
- Filter fastq files based on command line options
- Return True iff the time range is less than tto
nanofilt Key Features
nanofilt Examples and Code Snippets
Community Discussions
Trending Discussions on nanofilt
QUESTION
I would like to mix shell command in environment conda with any Python scripts, so the use of the 'run' section isn't possible ...
I tried :
...ANSWER
Answered 2020-Sep-17 at 15:44Snakemake shell doesn't support bash syntax for loops. I see two possible solutions.
First, you may wrap this code into a .sh file and run that from the shell
section:
QUESTION
I have a series of rule leading into using vsearch, with the barebones shown here:
...ANSWER
Answered 2020-Jul-17 at 08:40I would move seqkit fq2fa
to its own rule producing the temp
file nedded by vsearch
. Like (not tested):
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