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CRISPR and single-cell sequencing pinpoint causal genetic variants for traits and diseases: STING-seq provides roadmap to identify variants and genes, enabling deeper understanding of the noncoding genome and targets for therapies

CRISPR and single-cell sequencing pinpoint causal genetic variants for traits and diseases: STING-seq provides roadmap to identify variants and genes, enabling deeper understanding of the noncoding genome and targets for therapies
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CRISPR and single-cell sequencing pinpoint ca

A major challenge in human genetics is understanding which parts of the genome drive specific traits or contribute to disease risk. This challenge is even greater for genetic variants found in the 98% of the genome that does not encode proteins. A new approach developed by researchers at New York University and the New York Genome Center combines genetic association studies, gene editing, and single-cell sequencing to address these challenges and discover causal variants and genetic mechanisms for blood cell traits.

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Clarapath Acquires Crosscope

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Clarapath Acquires Crosscope and Combines Tissue Processing Robotics with AI Powered Digital Pathology for Building the Lab of the Future

/PRNewswire/ Clarapath, a robotics company aimed at catalyzing change in the way pathology laboratories process human and animal tissue, today announced the.

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The New York Genome Center Launches the MacMillan Center for the Study of the Non-Coding Cancer Genome

/PRNewswire/ The New York Genome Center (NYGC) announced the launch of the MacMillan Center for the Study of the Non-Coding Cancer Genome (MCSNCG) today, a.

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