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Discover how to leverage large biobanks for genetic studies of human traits and diseases with Wei Zhou from Broad Institute, MGH, and Harvard Medical School in this informative primer session.
Explore tissue-specific transcriptomes for drug target prioritization and disease risk prediction. Learn about TWAS, co-localization, polygenic risk scores, and phenome-wide scans in genetics research.
Explore how engineering approaches yield new perspectives on biological systems, enabling innovative measurements and insights into cellular and tissue function.
Discover how agricultural biotechnology innovations move from public domain to practical field applications, exploring adaptation and adoption strategies for enhanced farming practices.
Discover cutting-edge single-cell multiome technology and analysis methods for medical and population genetics research, focusing on complex trait genetics and human population studies.
Dive into advanced techniques for long-read whole genome sequencing analysis, covering data processing methods and analytical approaches for medical and population genetics research.
Discover cutting-edge single-cell multiome technology and analysis methods for medical and population genetics research, focusing on complex trait genetics, human variation, and disease studies.
Explore the Genomics2Proteins portal to visualize genetic variations, protein features, and functional data on protein structures for genomic research.
Discover seqr, Broad Institute's open source platform for rare disease genomic analysis, covering data loading, variant search, and clinical interpretation tools.
Master CellProfiler's free, open-source software for quantitative biological image analysis through hands-on tutorials covering pipelines, machine learning, and morphological profiling.
Dive into Illumina Genome Analyzer chemistry, workflows, sample prep, cluster generation, sequencing protocols, and data analysis through hands-on labs and expert guidance.
Discover Silvia Restrepo's inspiring journey studying plant pathology in Colombia and her path to leading the Boyce Thompson Institute in this LatinX@Broad speaker series.
Discover genetic subtypes of obesity and their functional implications in this scientific symposium presentation by Ruth Loos from the University of Copenhagen.
Discover how disentangled representations of single nucleus epigenomes advance variant interpretation in genomic medicine through computational biology approaches.
Discover how to engineer bespoke genome editing therapies and translate genetic associations into actionable therapeutic targets for personalized healthcare applications.
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