Spatial and Single Cell Diversity of Cells and Humans
Explore spatial and single-cell diversity in humans, examining how our surroundings influence cellular and individual variations through cutting-edge genomic research.
MPG Primer: Sequencing and Analysis of Long-Read Whole Genome Data - 2024
Explore long-read whole genome sequencing and analysis techniques, focusing on advanced methods for medical and population genetics research.
Deep Learning Models for Genomes and Beyond
Explore deep learning models for genomic analysis and their applications beyond, presented by Olga Troyanskaya in this Broad Institute colloquium on AI in biomedicine.
Decoding Cell Fates through Single Cell Genomics, Imaging, and Machine Learning
Explore decoding cell fates using single-cell genomics, imaging, and machine learning techniques in this cutting-edge symposium presentation by Dr. Jian Shu.
Human Brain Chimeroids as Avatars to Study Interindividual Variation in Response to Disease Risk
Explore human brain chimeroids as avatars for studying interindividual variation in disease risk response, presented by Harvard's Paola Arlotta.
Alpha Missense: Proteome-Wide Missense Variant Effect Prediction
Explore Alpha Missense, an AI model predicting missense variant pathogenicity. Learn how it combines structural context and evolutionary conservation to achieve state-of-the-art results in genetic benchmarks.
Defining Disease Variant Function with Single Cell Multimodal Sequencing and Gene Editing
Explore disease variant function through single cell multimodal sequencing and gene editing techniques in this cutting-edge symposium presentation.
The Future of Human Genetics - Discussion and Opening Remarks
Explore the future of human genetics through expert discussions and insights from leading researchers at the Broad Institute's Variant to Function Symposium.
Variant-to-Function in Obesity Research: Challenges and Opportunities
Explore challenges and opportunities in obesity research through variant-to-function approaches with insights from a leading expert in genomic mechanisms of metabolic disease.
Neuronal Modeling and Therapeutic Profiling of Alterations to Genome Structure and Function
Explore neuronal modeling and therapeutic profiling of genomic alterations with insights from Michael Talkowski's research at the Broad Institute.
Genomic Interpretation, seqr and Matchmaker Exchange - MPG Primer 2024
Explore genomic interpretation techniques, seqr software, and Matchmaker Exchange for advancing genetic research and diagnosis. Learn key tools for analyzing complex genetic data.
Linking Structure to Function in Metabolic and Blood Disorders Using Region Capture Micro-C
Explore linking structure to function in metabolic and blood disorders using Region Capture Micro-C, presented by PhD student Viraat Goel at the Broad Institute symposium.
Genetics of CAD and Its Vaccine Potential
Explore genetic factors of coronary artery disease, including DNA risk variants, HDL-C's role, and potential for risk stratification and primary prevention strategies.
Foundation Application to Link Spatial Transcriptomics to Clinical Images - Research Day
Explore a foundation application linking spatial transcriptomics to clinical images in cardiovascular research, enhancing understanding of molecular mechanisms in heart disease.
Redefining Precision in Precision Medicine - Learning from Gene Therapy Trials
Explore gene therapy trials and their impact on precision medicine, gaining insights into cutting-edge advancements in personalized treatment approaches.
Genetics of Atrial Fibrillation - DeBakey CV Grand Rounds
Explore the genetic factors underlying atrial fibrillation with Dr. Patrick Ellinor. Gain insights into cutting-edge research and its implications for cardiovascular medicine and patient care.
Cross-cohort Analysis via Cloud Genomics - MPG Primer
Dive into cross-cohort analysis using cloud genomics, exploring trusted research environments, methodologies, and tools for efficient genetic data processing and interpretation.
Stochasticity in Transcription - MPG Primer 2023
Dive into stochasticity in transcription, exploring single-cell data, dynamic regulatory elements, and transcriptional bursting in autoimmune diseases. Gain insights into modeling techniques and gene regulatory programs.
Base Editing and Prime Editing: Precise Genome Modification Without DNA Breaks
Explore groundbreaking gene editing technologies: base editing and prime editing. Discover their therapeutic applications and advancements in precision DNA modification without double-strand breaks.
Germline Variation and CRISPR Screens - MPG Primer 2023
Explore germline variation and CRISPR screens in this comprehensive primer. Gain insights into complex trait genetics, human genetic variation, and cutting-edge DNA sequencing methods.
MPG Primer: Intro to Terra - Hands on with Jupyter Notebooks in Terra - Part 2 of 3
Dive into hands-on Jupyter Notebooks in Terra with experts from the Broad Institute. Gain practical skills in medical and population genetics data analysis through interactive demonstrations and discussions.