41:03

Introduction to Metagenomics for Researchers

1:25:18

Interpreting Genomes for Rare Disease: Variant Interpretation - Steven Harrison, PhD

31:11

Introduction to RNA-Seq for Researchers

18:25

Use of Population Data in ACMG/AMP Sequence Variant Interpretation Criteria

31:26

Next Generation Sequencing 1: Overview - Eric Chow (UCSF)

43:12

Presentation - Use of the Genome Aggregation Database (gnomAD) (Anne O'Donnell-Luria)

51:48

Illumina Sequencing Overview: Library Prep to Data Analysis | Webinar | Ambry Genetics

59:10

Genetic Variant formats, and the Human Genome Variation Society (HGVS) nomenclature of variants