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Discover Affordable Custom NGS Panels
Thursday, February 12, 2015
IDT webinar helps NGS researchers bring cost-savings to target capture panels.

A Gene That Shaped The Evolution Of Darwin's Finches
Thursday, February 12, 2015
Researchers from Princeton University and Uppsala University in Sweden have identified a gene in the Galápagos finches studied by English naturalist Charles Darwin that influences beak shape and that played a role in the birds' evolution from a common ancestor more than 1 million years ago.

DNA ‘Cage’ Could Improve Nanopore Technology
Wednesday, February 11, 2015
Scientists at Brown University have designed a nanoscale cage that can trap a single DNA strand and allow before-and-after sequencing of the same DNA strand in research trials.

York Scientists To Map Haematological Cancer DNA
Wednesday, February 11, 2015
UK researchers have launched an ambitious project to analyse samples from over 20,000 blood cancer patients to identify how differences in their cancer cell’s DNA can influence the success of treatment.

Roche Acquires Signature Diagnostics
Tuesday, February 10, 2015
Acquisition will advance translational research for NGS diagnostics. Roche will leverage Signature’s unique expertise in both biobanks and next generation sequencing (NGS) assays to develop novel diagnostics for cancer patients.

Bioo Scientific and Icahn School of Medicine Partner
Tuesday, February 10, 2015
Bioo Scientific partners with the Icahn School of Medicine at Mount Sinai to reduce ligation bias in next generation sequencing.

Epigenetic Signatures that Differentiate Triple-Negative Breast Cancers
Tuesday, February 03, 2015
Australian researchers have identified epigenetic ‘signatures’ that could help clinicians tell the difference between highly aggressive and more benign forms of triple-negative breast cancer.

President Obama’s Precision Medicine Initiative
Monday, February 02, 2015
Details of President Obama’s Precision Medicine Initiative are unveiled.

New Techniques Reveal “Extreme” Gene Copy Range
Monday, February 02, 2015
New findings give scientists the first precise way to study places in the genome where the number of copies of a sequence varies widely from person to person.

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