Thanks westerman -- we modified for the new blast+ as below --
1) makeblastdb -in Trinity.fasta -dbtype nucl -parse_seqids -out TrinityBlast -title "All contigs"
2) blastn -query myfile.fa -db TrinityBlast -out myfile.out
3) same
4) blastdbcmd -db TrinityBlast -entry myid > found.fa
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Local db. Using the older version of blast (although blast+ is similar):
1) formatdb -i Trinity.fasta -p F -o T
2) blastall -p blastn -d Trinity.fasta -i myfile.fa -o output.blastn
3) manually look at output.blastn to figure out the id of the matching contig
4) fastacmd -d Trinity.fasta -s myid > found.fa
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Hey, Westerman in Purdue, thank you for you replying.Originally posted by westerman View PostBlast of your Trinity contigs against the partial sequence? Should be fast enough and sensitive enough to pick up the contig(s). Or am I missing something obvious here?
Are you talking about build a local db or www-blast something like that?
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Blast of your Trinity contigs against the partial sequence? Should be fast enough and sensitive enough to pick up the contig(s). Or am I missing something obvious here?
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How to dig out single particular gene from assembled contigs
Sorry if this question has been asked before. I just did a RNA-seq of a plant parasitic nematode species, and assembled 50,000 contigs by Trinity.
I would like to dig out a full-length sequence of endoglucanase gene, and do some protein structure prediction like that. Partial sequence of this gene was available through previous degenerate PCR. Does anybody know a easy and simple way to do it?
Thanks a lot.Tags: None
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