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Clinical OMICs – Molecular Diagnostics in Precision Medicine
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Molecular Dx
EVE AI Model Predicts Genetic Variants That Cause Disease
Bone Marrow Cancer
Cancer Drug Screening Method Finds One That May Be an Effective…
Precision Medicine
Cancer Cells Can Switch Macrophages from Tumor-Fighting to Tumor-Supporting
Bioinformatics
$2.1M Gift to Moores Cancer Center Launches Comprehensive Breast Cancer Database
Precision Medicine
Vertex Taps Mammoth’s CRISPR Tech in Gene Therapy Deal Worth up…
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Molecular Dx
EVE AI Model Predicts Genetic Variants That Cause Disease
Bone Marrow Cancer
Cancer Drug Screening Method Finds One That May Be an Effective…
Precision Medicine
Cancer Cells Can Switch Macrophages from Tumor-Fighting to Tumor-Supporting
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Digital PCR Leverages Microfluidic Array Tech
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![NGS technology has enabled researchers to epidemiologically analyze DNA sequences by quickly deciphering mass quantities of genetic information in a short amount of time. [Heart illustration: iStock/SvetaP DNA double helix: iStock/Kagenmi]](https://www.clinicalomics.com/wp-content/uploads/2019/01/304-324x160.jpeg "Study Supports Link Between SORBS2 and Congenital Heart Disease")
![A new technique to cheaply and rapidly create sets of DNA fragments that include all possible genetic variants will help scientists distinguish between genetic variants linked to disease and those that are innocuous. [Michael Worful]](https://www.clinicalomics.com/wp-content/uploads/2019/01/820-324x160.jpeg "More than 500 Structural Variants Linked to Hereditary Cancer and Cardiovascular Disorders Identified")
