Hello Sir,
I am doing reanalysis of your metatranscriptomics data. In raw metatranscriptomics files which were passed through quality control pipeline using #infrastructure-and-utilities:kneaddata Kneaddata, The output is concatenated and I want to seperate forward read (#0/1)and reverse read(#0/2). I could not understand how to identify some reads as they only had #0 at the end of the read ID.
Also please tell me if my consideration of forward read and reverse read ID is correct or not
Thank you
Yes, you are right about the forward read and reverse read ID. Can you point me out (link) to the raw metatranscriptomics files which have #0 at the end?
Hi @PRATIK_SHINDE and @sagunmaharjann,
I also downloaded these data from idbmdb. I understand the fastq files are interleaved paired end. Did you managed to understand what are the #0 reads?
Additionally, I’m wondering which preprocessing steps the reads were subjected to.
Thanks
Hello @Ish ,
You can check the respective sample files log file, available at ibdmdb for detailed preprocessing and for commands detail check kneadata manual
Apologies for the delay. I compared and tested a couple of MTX samples that you pointed out and the #0 are the forward reads “#0/1”. The old version of Kneaddata was somehow removing the “/1” from the forward reads during the merge.