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NEW YORK (GenomeWeb) – NextCode Health and the Simons Foundation Autism Research Initiative (SFARI) said today they have formed a partnership to help speed sequencing-related autism research.

Under the partnership, the Simons Simplex Collection (SSC), sequence and phenotypic datasets from nearly 2,600 families, will be available on NextCode Exchange, a newly launched genomic data analysis and collaboration service.

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An international commission is to develop a report on how researchers, clinicians, and regulators should evaluate the clinical applications of human germline genome editing.

The American Prospect writes that the pilot program to test the DNA of migrants could lead to more family separations.

The US Department of Agriculture presents a new blueprint for animal genomic research.

In Genome Research this week: repetitive element deletion linked to altered methylation and more in form of muscular dystrophy; human contamination in draft bacterial and archaeal genomes; and more.

Jun
17
Sponsored by
Illumina

This webinar will provide an overview of polygenic risk scores, which aggregate dozens of genetic variants that have been linked to disease risk in genome-wide association studies (GWAS) into a single score.