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Introducing Broad Genomics Blog
The Broad Institute has >25 years of experience in executing large-scale genomics projects to accelerate discovery in biomedical research. From the first human genome project to annually sequencing...
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Announcing Broad Clinical Labs
Introducing Broad Clinical Labs!The Broad Institute’s Clinical Research Sequencing Platform is now Broad Clinical Labs (BCL)! BCL aims to accelerate the understanding, diagnosis, and treatment of...
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Seeking Truth: Solving CNV Evaluation Challenges with T2T Genome Assembly
By: Yueyao Gao and Mark FlehartyCopy Number Variations (CNVs) are pivotal in shaping human genetic diversity and influencing disease susceptibility. These segments, either deleted (DEL) or duplicated...
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Single-Cell Isoform Sequencing of Fluent Libraries with MAS-seq
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Making the Most of Genome Sequencing: The Need for Detection of Sequence...
Author: Marina DiStefano Genome sequencing has opened opportunities for detecting multiple variant types across the genome with a single technology. Previously, BCL has tackled evaluating copy number...
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