Sequencing, Variant Calling, and Cancer Genomics Published 2021-06-17 Download video MP4 360p Download video MP4 720p Recommendations 52:46 "Circulating tumour DNA: An increasingly powerful diagnostic tool for oncology" - Nitzan Rosenfeld 55:42 Transitioning to GRCh38: Considerations and Challenges 35:36 BroadE: GATK - Intro to Somatic Variant Discovery 31:26 Next Generation Sequencing 1: Overview - Eric Chow (UCSF) 48:26 Jennifer Doudna: CRISPR Basics 55:29 Interpreting Genomic Variants for Inherited Cancer Risk and ELSI Considerations 51:02 25. Cancer 1 58:52 ctDNA and MRD | 2023 Best of GI Cancer Conference 05:50 Variants of Uncertain Significance 56:34 Cell‐Free DNA Sequencing for Early Cancer Detection 1:29:05 Concepts of Next Generation Sequencing 43:44 Presentation - Intro to Genome Analysis (Christina Austin-Tse) 53:04 Using BLAST for Genomic Sequence Annotation | Jeremy Buhler | GEP Training Workshop 2019 10:53 Investigating structural variations and complex cancer genomes using Oxford Nanopore sequencing 51:48 Illumina Sequencing Overview: Library Prep to Data Analysis | Webinar | Ambry Genetics 57:52 "Mitochondrial DNA variation in Human Origins and Disease" 43:26 Introduction to ACMG Genetic Variant Classification 48:03 WGS Variant Calling: Variant calling with GATK - Part 1 | Detailed NGS Analysis Workflow 1:13:46 Next-Generation Sequencing Technologies (2016) - Elaine Mardis 53:39 Basics of Exome Sequencing | Genetics 101 | Ambry Genetics Similar videos 03:49 Whole genome sequencing: From sample to report 17:25 Overcoming Challenges of Somatic RNA Variant Calling in Solid Tumors 01:58 Genomic Data Analysis: Breast Cancer : Oncogene Variant Calling 1:02:18 How to Read a Cancer Genome | Part 1: The basics of cancer genomics 19:03 Genomics England long-read cancer whole-genome sequencing pilot 31:06 Whole-Exome Sequencing to Identify Somatic Variants in Cancer - Yardena Samuels 01:01 The Role of Cancer Genomics & Whole Genome Sequencing in Diagnosis, Treatment & Prevention of Cancer 53:26 Sequencing analysis of cancer tissue samples: FFPE vs.Fresh Frozen 24:37 Bionano Genome Imaging 1:08:40 Methods in genomic variant calling 47:14 Somatic variant calling and interpretation in the Pan-Cancer... - Lincoln Stein - VarI - ISMB 2020 33:54 The Current State of Mutation Detection and Prospects for Long Read Sequencing 38:16 Large-Scale Cancer Genomics Data Analysis - David Haussler 36:56 Structural Variant Calling 01:15 How is genomics used in cancer care? 59:00 Revealing the Hidden Landscape of Structural Variants in Cancer Genomes 08:46 SAVANA: a computational method to characterise SVs in human cancer genomes using nanopore sequencing More results