Entering edit mode
4.9 years ago
baurumon
▴
30
HI,
I am using multiple alignment of non coding sequence to select conserved block. All the sequence has different length and when i run command : Gblocks result.pir -t=d -e=-gb1 -b4=5 -d=y, it is not accepting my data and showing---
Sequences with different number of positions. Execution terminated.
Is there any way to process data in Gblock?
Thanks in advance.
Have you tried to use the web interface to make sure your data is in correct format?
i tried it but did not work.
I converted my .fasta file to .pir with EMBL sequence conversion tool. https://www.ebi.ac.uk/Tools/sfc/ . Sequences look like as below-
Thank you @genomax