Closed cmkobel closed 4 years ago
It sounds like you are using a NextSeq 500 or similar which spreads all libraries over 4 lanes? We also use that. It's very annoying, so we changed the bcl2fastq
command to automatically create a single R1 file instead of 4 files L001 to L004.
Concatenating, which is as simole as cat blah*.fq.gz > blah.fq.gz
(no need to uncompress) is the easy solution but wastes disk space, at least temporarily.
Unfortunately, all the tools the nullarbor use will not support multiple lanes, they need a single R1 and R2. So i could add support to Nullarbor, but i would just be forced to make cat
copies. I think that is better done by you, s you may want to replace your 8 files with 1 permanently.
OK. I think I will write a wrapper that converts a custom-samples.tab with multiple lanes to a nullarbor-samples.tab, automatically merging the lanes and putting them in an adjacent folder.
Hello.
We often illumina-sequence in multiple lanes. This means that I have up to 8 paired end pairs which are independent but very relevant to combine, since a higher coverage is obtained through combination.
The format of the
samples.tab
-file seems to only support a single pair.Is there a straightforward way to supply multiple lanes of PE reads to nullarbor, or should I manually concatenate the lanes?