Comments (1)
implemented
from fastp.
Related Issues (20)
- I obtained different 'insert size peaks' when I used different options for the same paired-end sequencing sample.
- Insert size estimation and report interpretation HOT 2
- fastp in my pip package
- aborted core dumped
- Can fastp draw PNG format?
- Very short fragments
- No mouse ouver in kmer matrix
- Can fastq remove read sequences with duplicate IDs?
- Feature request: add option to set lower limit of unqualified quality
- Missing most reads after given r2 adapter HOT 1
- Interpretation help file?
- Store duplicate reads
- Split interleaved output
- interleaved output is not reproducible with multiple threads HOT 1
- Not able to install on Mac book M1 HOT 4
- Keep occurred error message from the beginning < igzip: invalid gzip header found >
- Nanopore data filtering using fastp
- No adapter detected for read and Q20 bases: 4747174600(99.9999%)
- fastp not removing all Illumina universal adapter sequences as indicated by FastQC HOT 2
- few options throw 'undefined error' -reg
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from fastp.