Thanks Asaf for your reply. The thing is I am currently working on a small dataset and I want to do this as an example for my next bigger dataset. So I don't really want to go through uploading big data files to Galaxy.
Hi every one,
I was wondering if somebody could tell me how to extract a number of genes from a number of fastafiles (all having the same set of genes) and CONCATENATE them altogether for each fasta file?
Having said that, I've got an excel sheet (or a text file) having the entities (the Start / End nucleotide positions) for every single gene.
I would like to do it using awk and grep in Unix.
Any help is appreciated.
Cheers,
Hossein
1 answer
so perl or python can give you the solution. In my opinion, if you don't master awk it's easier to learn perl or python and implement these small scripts than doing it in awk
Glad to hear that. I'll have start learning Perl or Python. So would you recommend me a webpage or textbook for learning Perl please? I appreciate your help. Regards. Hossein
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If I understand it correctly, think generating a bed file from your text file and after that bedtools getfasta associate with for loop may be a shot.