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Wellcome Sanger Institute

The researchers used SC3 to uncover subclones within samples from patients with pre-malignant tumors.

Researchers found mutations thought to be associated with embryo development and used them to recreate early cellular life in the human body.

Using a new mathematical model, researchers uncovered mutational signatures related to homologous recombination deficiency in up to one-fifth of breast cancers.

A retrospective analysis of Enterococcus faecium isolates from a UK hospital provided clues to infection sources and antibiotic resistance patterns.

The new sequences also uncovered two new gene families likely involved in Plasmodium malariae's ability to invade host cells.

Investigators uncovered 33 hotspots of large tandem duplications among breast cancer cases that affected cancer susceptibility genes and super-enhancers.

The researchers said their one-step, inducible, multiplex gene knockdown and gene knockout platforms can be used in many differentiated cell types.

The Bridget Ogilvie Building will house sequencing facilities, and the Biodata Innovation Centre will host genomic startups.

Two new studies are exploring genomic features and population variation in the river blindness-causing parasite Onchocerca volvulus.

A sequencing study suggests multidrug-resistant Mycobacterium abscessus bacteria are often passed between people, not acquired from the environment.

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The US National Institutes of Health's All of Us project awarded $4.6 million to the company Color to develop a genetic counseling resource for the program.

The Times of India reports on a pilot study that used genomic testing to determine whether patients had drug-resistant tuberculosis.

New guidelines say that more women may benefit from genetic testing for hereditary breast or ovarian cancer, according to the Los Angeles Times.

In Cell this week: small proteins identified among human microbiome, role for tumor microbes in pancreatic cancer survival, and more.