Closed pclavell closed 1 month ago
Hi,
Well, yeh, those readIDs are simply not extracted from a fastq. There is honestly no good reason for that :-)
Are you using --fastq
or --fastq_rich
? Do you only need the tsv file? That is --raw
I assume?
Wouter
I am using --fastq. Yes I only use the tsv from --raw
Okay, then I don't have to change NanoPlot to help you. I have added a much trimmed-down version of the code to the scripts: https://github.com/wdecoster/NanoPlot/blob/master/scripts/fastq_to_tsv.py Does that work for you?
Currently, it is single-threaded, as I don't know if you have a ton of data to process, but perhaps this is fast enough.
Hey, yes it works, thanks a lot! Let's see how does it perform with 15M reads fastq (I have 45 of them)
Hello, I have been doing a couple of nanoplot tests as I want to add it as QC in a nanopore pipeline. When I run nanoplot on ubam, I get a file called {my_sample}-data.tsv.gz with readID quals length. However, when I run it with fastq, the readIDs are not reported. I need them because I appended extra information to the readID to be able to stratify qualities by other parameters such as if a read is a duplex or a simplex, and other custom stuff. Do you know what could be happening?
Thanks a lot