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In Nature this week: genome-editing to treat hearing loss in mice, juvenile myelomonocytic leukemia subgroups, and more.
Peking University researchers performed single-cell methylome sequencing on preimplantation cells to examine DNA methylation changes during early development.
The SBIR grant will support the development of the firm's single-cell analysis platform, Tapestri.
Research teams documented mosaic mutations during brain development, as well as rising somatic mutations in aging brains or brains affected by neurodegenerative disease.
Using RNA sequences for thousands of cells, researchers looked at head and neck squamous cell carcinomas and proposed streamlined expression subtypes.
Broad Institute researchers performed RNA-sequencing of 53,000 individual mouse gut epithelial cells to develop and examine expression signatures.
The NIH has awarded $169 million this year to support 110 new projects in the Brain Research through Advancing Innovative Neurotechnologies Initiative.
The funding is being awarded under the auspices of the NIH's BRAIN Initiative Cell Census Network, which aims to establish reference cell atlases of the brain.
The startup will use the funds to commercialize its single-cell analysis platform, which is based in part on droplet microfluidic technology licensed from UCSF.
In Science this week: ancient Neanderthal and human genomes, and more.
The Washington Post reports on researchers' efforts to determine the effect of an increasingly common SARS-CoV-2 mutation.
Florida Politics reports Florida's law barring life, long-term care, and disability insurers from using genetic information in coverage decisions went into effect at the beginning of July.
A new analysis finds a link between popular media coverage of a scientific study and how often that paper is cited.
In Nature this week: CRISPR approaches to editing plant genomes, way to speed up DNA-PAINT, and more.