The Human Genetics Amplifier (HuGeAMP) is a software platform and infrastructure that aggregates, integrates, and analyzes human genetic and genomic data to spark insights into complex diseases.

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The Knowledge Portal Network (KPN) is an ecosystem of interconnected web portals that facilitate innovative and intuitive analysis and visualization of biomedical data.
BYOR.SCIENCE

The Bring Your Own Results (BYOR) service is an open-access platform that allows researchers to upload, visualize, analyze, and share their results.  Visit BYOR.SCIENCE

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Front page 2022

Knowledge Portal Network

Aging Knowledge Portal
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Association to Function Knowledge Portal
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Vision Genomics Portal
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Kidney Disease Knowledge Portal
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Autoimmune Disease Knowledge Portal
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Ocular Knowledge Portal
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Reproductive System Knowledge Portal
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Sleep Disorder Knowledge Portal
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Type 1 Diabetes Knowledge Portal
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Type 2 Diabetes Knowledge Portal
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Cardiovascular Disease Knowledge Portal
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Cerebrovascular Disease Knowledge Portal
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Common Metabolic Diseases Knowledge Portal
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Lipid Droplet Knowledge Portal
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Lung Disease Knowledge Portal
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Musculoskeletal Knowledge Portal
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Neurodegenerative Disease Knowledge Portal
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Non-Additive Genetic Effects Knowledge Portal
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Collaborate on methods
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Collaborate to create a new Knowledge Portal
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BYOR Data Pages and Portals

Rare variants with large endophenotype-derived effect sizes
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Vision Genomics Portal
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The APOL1 Portal
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Catalog of vQTLs and GxEs for cardiometabolic biomarkers
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Genetic Loci Clustering
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Curated T2D effector gene predictions
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Broad CVDI Human Disease Portal
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Effector index predictions
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Integrated Classifier T2D effector predictions
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Contribute results
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Create your own Research Page or Research Portal
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What's new

You can now export variant counts for multiple genes in one easy step! While each Gene page has a Download CSV option for downloading the variant table, sometimes you may want to do this for several genes at once. This functionality is now available via Multiple Gene Download (listed under Tools), where you can generate a filtered variant table for more than one gene and then download it. Additionally, read traces have been added to the Variant pages!

As you are aware, musculoskeletal diseases are widespread and disabling, yet there’s no centralized platform for musculoskeletal omics data and no curative treatments. We're building a knowledge base to fill this gap, The Musculoskeletal Knowledge Portal (MSKKP; mskkp.org), which focuses on advancing discovery, uncovering disease mechanisms, and helping identify therapeutic targets. The MSKKP has been funded for an additional four years via the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS). 

Headed to ISMB? Check out our platform talk as part of the NIH Track on GenAI, Cyberinfrastructure, Digital Twins, and Quantum Computing!
Unlock the future of fat: join our Focus Group on July 10th, 2025 to review two cutting-edge open access portals in Adipose Tissue Biology.