Closed methylnick closed 6 years ago
@methylnick sorry taking it a while to get back to you. RNAsik
should handle this fine. I might have made some improvements in the last couple of month, so best to grab latest version.
Use these options when running RNAsik
-pairIds "_1,_2" -extn "fq.gz"
Let me know how it goes
Cheers
@methylnick going to close this issue as I think it should all work and not actual bug/problem with the code. Feel free to reopen if needed.
Cheers
It appears with BGI, they have their own result output structure. Which has some implications with RNASik and how it handles such files.
please see this path:
/mnt/cephfs/scratch/nick.wong/alison.anderson/cdts-wh.genomics.cn/F18FTSAPHT0121_HUMxcaE/Clean
Differences are, each sample is a folder. Within each folder is the fastq file name which is a different structure than normal Illumina data.
CL100059708_L2_WHHUMxcaEAABRAAPEI-543_1.fq.gz
_1 is the read id 543 is the sample number the preceding characters are the machine and flowcell it would seem.