NEW YORK (GenomeWeb News) – Investigators in the UK and the Netherlands have partnered to use genome sequencing to uncover genomic and biochemical characteristics of four human cancers and to screen drug combinations aimed at creating personalized treatments.

The researchers at the Wellcome Trust Sanger Institute and the Netherlands Cancer Institute, or NKI, have been awarded a £14.5 million ($18.9 million) Synergy grant from the European Research Council to fund the effort, which is part of the ERC's CombatCancer initiative, the European Commission said yesterday.

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In Nature this week: method to detect single-nucleotide and copy-number alterations in single cells from archival tissue, and more.

China has announced new rules governing the use of stem cell treatments, Nature News reports.

Wired's Sarah Zhang expresses frustration as a microbiome study of homes uncovers expected bacteria.

A database containing genome sequences from strains of foodborne pathogens may enable regulators and companies to quickly identify outbreak sources, Reuters reports.

Sep
17
Sponsored by
Omicia

This online seminar will provide examples of how commercial and hospital-affiliated clinical labs are successfully developing and deploying high-throughput next-generation sequencing-based testing services for genetic diseases. 

Oct
15
Sponsored by
Parabase

This webinar will discuss the benefits of a rapid targeted next-generation sequencing (TNGS) panel, using dried blood spots, for second-tier newborn metabolic and hearing loss screening and its immediate utility for high-risk diagnostic testing in the neonatal intensive care unit. 

Oct
29
Sponsored by
Lucigen

This webinar will focus on a range of research and clinical applications enabled by improvements in mate pair technology for whole genome sequencing.