Joe Diano asked 7 years ago
Hi
Just wondering as I am new tothe NGS world. What would be a good online resource for answering this type question:
“Understand the processing of MPS data including the demultiplexing of samples, alignment of sequence data, variant calling data annotation (minor allele frequency, mutational consequence using in silico prediction tools), using variant web-based databases to determine the presence of the variant in control and disease populations etc”
Any help is much welcomed
and thank you in advance
Cheers
Joe