Closed ckhithesh closed 4 years ago
Unfortunately you will have to specify the regions with -w
.
Dear Team, Any suggestion on parameters for SNP calling (multiple contigs). Regards Hithesh
It is hard to help without information about your sample and sequencing data so I suggest using the defaults.
Dear Simpson, My sample details are 6 samples. where a sample consists of 5 amplicons and I have to call variants of all 5 amplicon in a sample. As if I used -w it will work for specific region. How to retrieve variants for 5amplicons from a sample. Regards Hithesh
Hi,
You will have to run nanopolish 5 times, once for each region.
Jared
Dear Jared, Thank you for the reply! I have one more question regarding the variant call for the complete genome. I have a genome of around 500 scaffolds. So, please let me know how to do for this?
Regards Hithesh
Hi @ckhithesh,
We provide an example of running over many windows of a genome here:
https://github.com/jts/nanopolish#computing-a-new-consensus-sequence-for-a-draft-assembly
This is for consensus calling but you should be able to adapt it to call variants instead (remove the --consensus
flag, add any other options you need).
Jared
Hi team, I'm looking to call the variants from multiple amplicons in single sample. Clearly a sample contains 10genes to call variants using nanopolish variants. And I don't want to mention the regions (-w).
Thanks in advance Regards Hithesh