Transform Sequencing Data into Actionable Genetic Insights
Transform Sequencing Data into Actionable Genetic Insights
Transform Sequencing Data into Actionable Genetic Insights
The Computational Genome Analysis Platform (CGAP) is an intuitive, open-source analysis tool designed to support complex research & clinical genomics workflows.
The Computational Genome Analysis Platform (CGAP) is an intuitive, open-source analysis tool designed to support complex research & clinical genomics workflows.
The Computational Genome Analysis Platform (CGAP) is an intuitive, open-source analysis tool designed to support complex research & clinical genomics workflows.
A unified workflow for clinical & research use-cases
A unified workflow for clinical & research use-cases
A unified workflow for clinical & research use-cases
We are implementing powerful variant discovery & diagnostic tools for individual samples and cohorts with clinical accuracy and reporting capabilities in one platform.
We are implementing powerful variant discovery & diagnostic tools for individual samples and cohorts with clinical accuracy and reporting capabilities in one platform.
We are implementing powerful variant discovery & diagnostic tools for individual samples and cohorts with clinical accuracy and reporting capabilities in one platform.
GENOMIC MEDICINE
GENOMIC MEDICINE
Interactive Family Collection and Phenotyping ACMG Guideline-Based Intepretation & Reporting CLIA-Compatible Workflow
Interactive Family Collection & Phenotyping ACMG Guideline-Based Intepretation & Reporting CLIA-Compatible Workflow
Interactive Family Collection & Phenotyping ACMG Guideline-Based Intepretation & Reporting CLIA-Compatible Workflow
GENE DISCOVERY RESEARCH
GENE DISCOVERY RESEARCH
Robust Knowledgebase of Genomic Variants Flexible Filtering and Interpretation Tools Easy Data-Sharing and Collaboration
Robust Knowledgebase of Genomic Variants Flexible Filtering and Interpretation Tools Easy Data-Sharing and Collaboration
How does CGAP Work?
How does CGAP Work?
How does CGAP Work?
CGAP is a complete End-to-End Solution for Case & Cohort Analyses
CGAP is a complete End-to-End Solution for Case & Cohort Analyses
CGAP is Empowering Innovative Research & Clinical Care Collaborations
CGAP is Empowering Innovative Research & Clinical Care Collaborations
CGAP is Empowering Innovative Research & Clinical Care Collaborations
Undiagnosed Disease Network (UDN)
The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples and facilitate discovery across the UDN Cohort.
Multiple System Atrophy (MSA) Coalition
The MSA Coalition leverages CGAP’s case and cohort analysis workflows to uncover the genetic causes of MSA.
Undiagnosed Disease Network (UDN)
The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples.
Multiple System Atrophy (MSA) Coalition
The MSA Coalition leverages CGAP’s case and cohort analysis workflows to uncover the genetic causes of MSA.
Brigham Genomic Medicine (BGM)
BGM is identifying novel gene-disease associations in patients and families with unsolved rare genetic diseases.
People Powered Medicine (PPM)
PPM used CGAP to identify the genetic variants associated with exceptional response to cancer treatments.
PROACTIVE Research Clinical Study
PROACTIVE has successfully identified all actionable germ-line variants across clinical cancer cases.
Undiagnosed Disease Network (UDN)
The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples.
Multiple System Atrophy (MSA) Coalition
The MSA Coalition leverages CGAP’s case and cohort analysis workflows to uncover the genetic causes of MSA.
Brigham Genomic Medicine (BGM)
BGM is identifying novel gene-disease associations in patients and families with unsolved rare genetic diseases.
People Powered Medicine (PPM)
PPM used CGAP to identify the genetic variants associated with exceptional response to cancer treatments.
PROACTIVE Research Clinical Study
PROACTIVE has successfully identified all actionable germ-line variants across clinical cancer cases.
Built in Partnership with Experts in Informatics & Genomics
Built in Partnership with Experts in Informatics & Genomics
Built in Partnership with Experts in Informatics & Genomics

Copyright 2022 President and Fellows of Harvard College. All Rights Reserved.

Copyright 2022 President and Fellows of Harvard College. All Rights Reserved.

Copyright 2022 President and Fellows of Harvard College.

All Rights Reserved.