Entering edit mode
5.7 years ago
O.rka
▴
740
I have some Otus that I suspect are contaminants from faulty primers. How can I blasted them against the nt database and the results look like this (w/ outfmt=6):
Otu000056 gi|1163074592|gb|CP020116.1| 99.52 209 1 0 4 212 4182852 4183060 4e-102 381
Otu000056 gi|1163034213|gb|CP020058.1| 99.52 209 1 0 4 212 2494582 2494790 4e-102 381
Otu000056 gi|1163027546|gb|CP020055.1| 99.52 209 1 0 4 212 2523673 2523465 4e-102 381
Otu000056 gi|1163005269|gb|CP020048.1| 99.52 209 1 0 4 212 2155734 2155942 4e-102 381
Otu000056 gi|1162933287|gb|CP020107.1| 99.52 209 1 0 4 212 559506 559298 4e-102 381
Otu000056 gi|1162922101|gb|CP020106.1| 99.52 209 1 0 4 212 5006373 5006581 4e-102 381
Otu000056 gi|1162894325|gb|CP020092.1| 99.52 209 1 0 4 212 4746448 4746656 4e-102 381
I have thousands of these hits. How can I go from gi|1163074592|gb|CP020116.1|
to Escherichia coli strain AR_0104, complete genome
for example w/ the actual annotated hit? Preferably a command line tool that I can just feed my blast6 output into if possible.