High-throughput Diagnostics and Sequencing at the Pandemic Response Lab NYC
Explore high-throughput diagnostics and sequencing for COVID-19 control, including testing methods, sample tracking, and variant monitoring at the Pandemic Response Lab NYC.
Overcoming Challenges in Semantic Alignment of Therapeutics Knowledge Using TheraPy
Explore semantic alignment challenges in therapeutics knowledge and learn how TheraPy can help overcome them in cancer genomics research.
Heterogeneity of Breast Cancer Genomes: Going Beyond Therapy to Risk Assessment and Prevention
Explore breast cancer genome heterogeneity, focusing on risk assessment and prevention strategies beyond therapy. Gain insights from expert Olufunmilayo Olopade at the CGC 2023 Annual Meeting.
Emerging Solutions for Non-Invasive Cancer Monitoring
Explore non-invasive cancer monitoring through liquid biopsy, focusing on Blocker Displacement Amplification technology for improved detection and longitudinal tracking of cancer biomarkers.
Exploring the Many Dimensions of Sex and Gender in the Genomics Era - Day 2, Part 3
Interdisciplinary symposium exploring complexities of sex, gender, and genomics. Experts discuss scientific, ethical, and historical contexts to aid understanding for scientists, policymakers, and the public.
Exploring the Many Dimensions of Sex and Gender in the Genomics Era - Day 1, Part 2
Interdisciplinary panel explores historical perspectives on sex categorization in biology and law, examining complexities and contradictions in scientific and legal definitions of sex.
Pathogen Evolution in the Context of Host and Environmental Adaptation
Explore pathogen evolution, host adaptation, and environmental factors shaping disease dynamics. Gain insights into emerging infectious diseases and their ecological impacts.
Tree-Free Phylodynamic Inference for Emerging Viral Pathogens and Lineages
Explore tree-free phylodynamic methods for analyzing emerging viral pathogens and lineages, focusing on innovative approaches to study viral evolution and spread.
Interpreting the Evolution of SARS-CoV-2 - Merigan Lecture
Explore the evolutionary journey of SARS-CoV-2 with expert insights from Prof. Jesse D. Bloom, delving into its mutations, adaptations, and implications for public health.
Pantheon DNA Data Storage CODEC: Experiences, Challenges, and Innovations
Dive into the groundbreaking world of DNA data storage through Pantheon CODEC, exploring synthesis technologies, error correction methods, and practical implementation challenges in cold-data storage systems.
WGS Variant Calling - Variant Filtering and Annotation - Part 2 - Detailed NGS Analysis Workflow
Detailed tutorial on filtering and annotating genetic variants using GATK tools. Covers hard filtering, genotype refinement, and Funcotator for comprehensive variant analysis in bioinformatics workflows.
Pseudo-Bulk Analysis for Single-Cell RNA-Seq Data - Detailed Workflow Tutorial
Comprehensive tutorial on pseudo-bulk analysis for single-cell RNA-Seq data, covering the what, why, and how. Includes data manipulation, aggregation, and differential expression analysis using R, Seurat, and DESeq2.
Find Markers and Cluster Identification in Single-Cell RNA-Seq Using Seurat - Workflow Tutorial
Comprehensive tutorial on identifying cell markers in single-cell RNA-Seq data using Seurat, covering various marker identification methods, data visualization, and cluster annotation techniques.
DESeq2 Basics Explained - Differential Gene Expression Analysis - Bioinformatics 101
Comprehensive guide to DESeq2 for differential gene expression analysis in RNA-seq data, covering statistical models, normalization methods, and key steps in the analysis pipeline.
How to Analyze Single-Cell RNA-Seq Data in R - Detailed Seurat Workflow Tutorial
Comprehensive tutorial on analyzing single-cell RNA-Seq data using Seurat in R, covering data processing, quality control, normalization, dimensionality reduction, and clustering for genomics research.
EdgeR and DESeq2, Part 2 - Independent Filtering
Explore edgeR and DESeq2's approaches to filtering low-count genes in RNA-seq analysis. Learn about false positives, FDR, CPM, and sequencing depth impacts on gene expression studies.
Bioinformatics and Computational Terminology for the Clinic - Webinar - Ambry Genetics
Demystifying bioinformatics concepts in genetic testing reports, focusing on key terminology and underlying details for NGS panel and exome-sequencing tests to enhance clinicians' understanding and interpretation.
Rigidity Theory for Gaussian Graphical Models - The Maximum Likelihood Threshold of a Graph
Explore rigidity theory's application to Gaussian graphical models, focusing on maximum likelihood thresholds and their implications for data analysis in genomics and other fields.
NGS Analysis Practical Using Galaxy Server - Section 1
Hands-on demonstration of NGS analysis using Galaxy server, covering step-by-step procedures and providing practical insights for bioinformatics researchers.
Low Rank Tensor Methods in High Dimensional Data Analysis
Explore low rank tensor methods for analyzing high-dimensional data in various fields. Learn about recent progress, challenges, and applications in extracting information from multilinear arrays.
Data-Driven Discovery: Revolutionizing Medical Research
Discover how big data and outsourced research are revolutionizing scientific inquiry, challenging traditional methods, and unlocking new possibilities in genomics and medicine.