Presentation - Use of the Genome Aggregation Database (gnomAD) (Anne O'Donnell-Luria) Published 2021-02-24 Download video MP4 360p Download video MP4 720p Recommendations 10:34 Q&A - Use of the Genome Aggregation Database (gnomAD) (Anne O'Donnell-Luria) 43:44 Presentation - Intro to Genome Analysis (Christina Austin-Tse) 37:23 Presentation - Variant Classification using ACMG/AMP Guidelines (Steven Harrison) 1:05:39 Overview of ACMG/AMP v4 Sequence Variant Guidelines 12:41 Curing Disease With Genetics And AI 31:26 Next Generation Sequencing 1: Overview - Eric Chow (UCSF) 40:16 MPG Primer: gnomAD v4: Behind the scenes (2023) 15:54 ACMG AMP guidelines overview and optimization 41:03 Introduction to Metagenomics for Researchers 1:03:50 Expression vectors: how to choose, or customize, vectors for gene & protein expression 59:17 HGVS nomenclature basics and legacy variants 39:30 Howard Chang (Stanford, HHMI) 1: Epigenomic Technologies 54:20 The New Approach to Co-segregation for Variant Classification 3:09:11 Power BI Dataflows Tutorial and Best Practices [Full Course] 📊 1:01:46 Genome vs Exome sequencing; everything you should know 57:33 Presentation - Hands on Variant Curation Interface Training (Steven Harrison & Matt Wright) 12:49 Introduction to Variants and Nomenclature 1:08:40 Methods in genomic variant calling 50:32 Review of the ACMG/AMP variant interpretation guidelines 3:54:38 Optogenetics: Illuminating the Path toward Causal Neuroscience Similar videos 43:12 H3Africa: Presentation - Use of the Genome Aggregation Database (gnomAD) (Anne O'Donnell-Luria) 47:03 ExAC and gnomAD 57:55 Annotation Data and its Uses - Anne O’Donnell-Luria, MD, PhD 44:30 MPG Primer: Using gnomAD - Tips and Tricks (2020) 54:21 MPG Primer: gnomAD: Using large genomic data sets to interpret human genetic variation (2019) 50:51 Updates to the gnomAD resource - STRs, variant co-occurrence and other tips. 52:28 MPG Primer: ExAC & gnomAD: Using large genomic data sets to interpret human genetic variation (2017) 09:36 H3Africa Hands-On Workshop 2022 - GREGoR Collaborations (Anne O'Donnell Luria) 44:56 Constraint scores 1:02:23 MPG Primer: Clinical interpretation of genes and variants for disease causality (2022) 23:42 "Data sharing in rare disease genomics" Anne O´Donnell-Luria, 27.10.2021 39:46 Presentation - Use of and Submission to ClinVar (Melissa Landrum) 49:45 MPG Primer: Modeling rare variation and calculating genetic constraint (2023) 05:02 Genetic Variant Databases 09:09 Q&A - Copy Number Variant Interpretation/Dosage Sensitivity Curation (Erica Andersen) 59:01 Science for All Seasons: What will it take to make clinical genomics part of everyday medicine? More results