Healthcare providers need a clinical genomic sequencing partner that is easy to work with and consistently delivers quality results, on time.
The Broad’s clinical sequencing service includes a provider portal with API support for easy order entry, access to reports and raw data, and contact with customer support. Our streamlined process ensures that you receive actionable data within a guaranteed 28-day timeframe.
Our clinical sequencing platform supports two accredited workflows: whole genome sequencing (WGS) and whole exome sequencing (WES). All data is shared with the submitting institution to enhance clinical interpretation.
Let’s discuss how we can streamline access to genomic data to support patient care.
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As part of our commitment to providing unsurpassed excellence in sequencing, the Broad Institute now offers services utilizing the improved capabilities of the Illumina® NovaSeq X platform.