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2.6 years ago
Human
•
0
I am searching for a smart way to reconstruct a sequence next to a gene of interest to set primers. For this I want to use the sequence of a gene from NCBI, search for it in my raw fasta files, and in case of a perfect match, get a part of the neighboring sequences as well.
So far I'm using this one liner:
perl -lane ' if ($_ =~ "sequence xy") {@array=split("right part of sequence xy"); print $array[1]}
But like this I don't know when the gene actually ends and also I don't know how to go "to the left side".
Maybe there is a smarter solution to do it with one command only.
Thanks in advance!
If you have some sequencing reads, why don't you assemble them first into contigs and then check if your gene sequence can be aligned to the assembly?
Basically I need a code to check if a sequence (a sex specific gene) is present in a huge pool seq fasta file, and see a portion of the neighboring sequences as well (left and right next to the sequence I searched for). What would you recommend?