Hi Everyone,
We are looking at 'loss of function' variants in the human genome. I am using a program called 'ALoFT' to identify LoF variants....
4 results in 0.0021 seconds.
-
Has anyone here used ALoFT with GRCh38 ?
-
align reads generated with Nextera exome kit (designed on GRCh37) to GRCh38?
Dear all,
in my lab we are using the Nextera Rapid Capture Exome kit to do whole exome sequencing. Until now I have used GRCh37 as a reference... -
running Grch37 to grch38 liftover tool locally
Hi all,
I am trying to run the UCSC ligtover tool on my local machine (linux version), but am running into some difficulties.
... -
Not a Big Deal, GRCh38: A Semi-Casual Comparison of the New Human Reference Genome
Over christmas GRCh38, the newest human reference genome assembly, was released.Internally we have been using chromosome 20 of human reference builds...
