Thanks Mikhail for the answer. Could you please let me know whether its possible to assemble the entire genome only from the contigs. Actually, I am new to this area and I hope you will answer accordingly. What I have with me is only a file containing contigs and I don't know whether they are paired-end or not ? I don't even know whether paired end reads are required for further assembly or not ??
Hello,
I have a query regarding identifying genes from the transcriptome data of a fungi. I got a fasta file containing contigs from my lab member and I need to identify the genes of my interests from those contigs.
What I have done so far is that I have performed blastx of the all the contigs againts nr database. I got the match for the contigs but I am confused with the query frames, as sometimes they are negative? More over when I take a positive frame as per the hit, I get some translated protein sequence which matched to the hit but the match is never complete because I get stop codons in between. So I am confused whether I am doing it the right way or not?
Any help would be appreciated.
Regards BHARAT
1 answer
Check out Transdecoder and other downstream analysis options from Trinity pipeline.
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