|
|
|
|
|
by adenadel
3885 days ago
|
|
With particular hardware and software you can. Edico Dragen claims speeds for bcl -> vcf of 20 minutes [1]. With Microsoft Research's snap aligner and 450GB of memory you can get whole genome alignment in ~30 minutes and then variant calling can be done in a couple hours. 1. http://www.edicogenome.com/dragen/dragen-gp/ |
|