NEW YORK (GenomeWeb News) – GenoSpace, PathGroup, and Thomson Reuters' IP & Science business today announced an initiative aimed at personalized medicine in oncology.

The partners will combine their resources, technologies, and expertise to integrate PathGroup's SmartGenomics next generation DNA sequencing and cytogenomic array with traditional pathology assays, enabling genetic profiling that may lead to greater insights into disease and patient treatment options, they said.

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In PLOS this week: gene fusion in premature ovarian failure, population patterns in the Franciscana dolphin, and more.

A National Science Foundation-funded project aims to give researchers access to a network many times faster than the Internet.

Bioethicists weigh the idea of charging patients to take part in clinical research, coming down against the approach.

Cornell's Christopher Mason and his colleagues correct their New York City microbiome study to emphasize "the difference between matching fragments of DNA from a species and a pathogen."

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.