Comments (6)
Is the -c command the same as the -r for read removal in Nanolyse?
Yes that is correct.
Can it generate a log file of how many reads were removed due to low quality, length, and host contamination?
I agree that would be useful. Easiest to implement would be a total number of reads that were removed, less straightforward would be to identify for which reason a read got removed. I will put it on my to-do list.
Cheers,
Wouter
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From version v0.4.0 the tool will write to stderr how many reads were kept from the total number of reads. You can redirect this to a file as below:
zcat reads.fastq.gz | chopper -q 12 2> chopper.log | gzip > filtered.fastq.gz
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Oof, I identified a bug, and I will push a fix later tonight. Thanks for reporting!
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I created v0.5.0, for which you can download a binary from the releases, but it will take a few hours before that makes its way into bioconda.
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Related Issues (20)
- sequencing_summary.txt feature HOT 1
- error: Found argument 'file.fastq' which wasn't expected, or isn't valid in this context HOT 8
- /lib64/libc.so.6 issue HOT 5
- Filter out reads marked as contaminants? HOT 1
- Cannot Download Chopper HOT 4
- Nanopore barcode/adapter detection HOT 2
- Give minimap more threads when available. HOT 4
- missing ".with_cigar()" in Aligner? HOT 7
- Recommended defaults? HOT 5
- Issue in Installation HOT 7
- Not running on aarch64 HOT 11
- Not working on M2 Mac HOT 6
- Help with --contam parameter HOT 1
- chopper with bam files HOT 1
- Instatlation issue HOT 2
- confuse problem HOT 10
- minimap2 preset for `--contam` HOT 9
- chopper v0.8.0 GLIBC_2.XX not found HOT 2
- Cannot use either wget, conda, or mamba to install chopper HOT 7
- --contam :Filter contaminants against a fasta
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