Regional missense constraint improves variant deleteriousness prediction
59:06
MPG Primer: Analysis of rare variants from sequencing studies (2016)
1:50:01
Finding Somatic Mutations in Cancer Genome Sequence Data
1:05:39
Overview of ACMG/AMP v4 Sequence Variant Guidelines
50:42
[TALK 18] Using Proteome Discoverer to Interrogate your Data – Cat Franco
37:03
Sanger Seminar - Functional genomic approaches to guide cancer drug discovery - Dr Mathew Garnett
52:59
Assessment of case control studies for the ClinGen Gene Disease Clinical Validity Framework
25:21
Identifying repeat expansions in short read sequencing: Compassion of tools
31:29