Comments (7)
I just found the same bug today, and I've applied a quick fix. you may try it: https://github.com/hliang/seqtk
.
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@hliang tried the version in your repository, but didn't work. The pair information was still missing:
$ git clone https://github.com/hliang/seqtk
$ ./seqtk
Version: 1.0-r32
$ seqtk sample -s100 read1.fastq.gz 10000 > test.fastq
$ head test.fastq
@H108:305:C0HA1ACXX:1:1107:13912:126962
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Could you include a section of the original FASTQ file for my testing? It worked on a trivial test case on my end.
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Please try the latest version.
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@vsbuffalo Sorry. Overlooked your pull request which does the same thing.
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@aleimba oh, sorry, I mean the same issue in subseq
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@vsbuffalo @lh3 everything works in the seqtk-master branch now. Thanks a lot for your fast response guys!
P.S.: I'm very new to github, didn't know a pull request can be equivalent to a fix, sorry.
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Related Issues (20)
- make warning HOT 4
- seqtk subseq in.fq name.lst > out.fq didn't work HOT 4
- Merging multiple fastq.gz files HOT 2
- Seqtk trimfq used on files in .gz format returns much larger files but still .gz HOT 1
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- cutN penalty to identify all Ns?
- feature request: ability to pass through all reads by specifying sample '1.0'
- subseq empty output
- seqtk sample: with out without replacement? HOT 1
- `seqtk seq` segfaults on 10G scaffolds HOT 4
- seqtk sample not working as expected HOT 2
- seqtk sample can't properly output fastq.gz HOT 1
- ERROR: the 2nd file has fewer records HOT 1
- The output file size of seqtk subseq is zero HOT 1
- Question: DNA string compressing HOT 1
- seqtk produces different number of reads for paired end files HOT 1
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- output file contains only one amino acid HOT 1
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