Hi,
I have a FASTQ file downloaded from SRA of paired 454 reads:
Each paired read is a single FASTQ record, including the linker sequence somewhere in the middle. What software can identify the linker and split the read into two FASTQ records? I've used sff_extract for SFF files, but the author has confirmed that it cannot handle FASTQ files.
Thanks,
Shaun
I have a FASTQ file downloaded from SRA of paired 454 reads:
Each paired read is a single FASTQ record, including the linker sequence somewhere in the middle. What software can identify the linker and split the read into two FASTQ records? I've used sff_extract for SFF files, but the author has confirmed that it cannot handle FASTQ files.
Thanks,
Shaun
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