You can upload your data and perform various analyses using a “drag and drop” user interface. Keep it private or share with collaborators. Bioinformatics tools and computational infrastructure are available for researchers who may not have programming expertise, or the time to pursue technical programming and/or scripting.
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All of your documents and content are private within a project unless you choose to share with others. It’s easy to add colleagues to your projects, change access privileges, and communicate with one another.
ClinGen
One of the main goals of the Clinical Genome Resource project is to enable curators and researchers to understand the clinical significance of genes, variants and genetic disorders. We contribute to this effort by developing several software products, web services and user interfaces to facilitate curation of genes and variants.
Learn more about our software products developed for ClinGen

The Human Epigenome Atlas contains human reference epigenomes and the results of integrative and comparative analyses. Atlas data provides detailed insights into locus-specific epigenomic states, including histone marks and DNA methylation across tissues, cell types, developmental stages, physiological conditions, genotypes, and disease states.
Image: National Institutes of Health
The goal of the ERCP is to better understand the fundamental biological mechanisms of extracellular RNA (exRNA) generation, secretion, and transport, to create a public dataset of where exRNAs exist in normal human body fluids, and to explore their potential as therapeutics and biomarkers.
Image: National Institutes of Health
One of the components of the Clinical Genome Resource project is ClinGenDB infrastructure to enable the development of a knowledge base about genetic variants of clinical significance. ClinGenDB infrastructure consists of databases and web services implemented using Genboree KnowledgeBase (GenboreeKB).
Image: National Institutes of Health
The goal of this consortium is to map DNA methylation, histone modifications, chromatin accessibility, and small RNA transcripts in tissues and organs frequently involved in human disease.
The Bioinformatics Research Laboratory (BRL) has developed Genboree and is comprised of bioinformaticians, software engineers, biologists, research scientists, graduate students, and interns. Projects span a variety of areas, including epigenomics, clinical genomics, cancer biology, metagenomics, algorithm development, and semantic web technology.
The Genboree Network is comprised of Genboree servers containing tools and services across the web that connect Genboree Workbench installations in different geographical locations via HTTP-based Application Programming Interfaces (APIs). The Genboree Network provides an innovative solution to problems hampering basic and translational applications of massively parallel sequencing: availability of bioinformatic tools for non-programmers, data access, access to cloud computing resources, web-based collaborative and data management resources.