I am having an assembled fasta file (~3.7 GB in size). I tried using the web based MISA v2.1, but it accepts fasta upto 2Mb only. Is there any other alternate software which can be used for a large size dataset for filtering SSRs?
If it is a fasta file and assembled, it can't be in GBs. There is something wrong. Check before your proceed.
Dear Nazima, You may consider GMATA tool. Article GMATA: An Integrated Software Package for Genome-Scale SSR M...
Thanks Anuj Kumar.. I tried using GMATA and was able to filter the SSR motifs... Moving on to the next step that is primer designing
Hi
You can also use the offline version of Misa. Click on "Download Sourcecode" in this page:
https://webblast.ipk-gatersleben.de/misa/
You should run it under perl. For example:
perl ./misa.pl
Regards
SciRoKo software, it also can extract flanking regions, and has an add on for creating primers
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