{% extends 'base.html' %} {% load static from staticfiles %} {% block extrahead %} {% endblock %} {% block content %}
Next Generation Sequencing (NGS) is a powerful diagnostic and research tool for Mendelian disease, but without proper tools, this data can be inaccessible to researchers. We are developing seqr as an open source web interface to make research productive, accessible, and user-friendly while leveraging resources and infrastructure at the Broad Institute.
Features:Developed at the Analytic and Translational Genetics Unit (ATGU) at Massachusetts General Hospital (MGH) in collaboration with the Broad Institute of Harvard and MIT, seqr is the analytic platform used by the Broad’s joint Center for Mendelian Genomics.