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BioWorld - Tuesday, March 31, 2026
Home » Topics » Diagnostics, Medical technology

Diagnostics, Medical technology
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hologic-3Dquorum-11-13.png

Following solid quarterly results, Hologic gains FDA nod for 3Dquorum imaging tech

Nov. 13, 2019
By Liz Hollis
Marlborough, Mass.-based Hologic Inc. got good news from the U.S. FDA, which has given the green light for the 3Dquorum imaging technology, which employs Genius AI. The technology works along with Hologic's Clarity HD high-resolution imaging technology to reduce tomosynthesis image volume for radiologists by 66%, the company said.
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DNA

FDA clears first whole exome sequencing platform for overall tumor mutation burden

Nov. 13, 2019
By Meg Bryant
Nanthealth Inc. has received U.S. FDA clearance for a whole exome sequencing test to determine overall tumor mutational burden (TMB) in cancer tissue. Known as Omics Core, the first-of-its-kind in vitro diagnostic test is available now as part of Nanthealth's GPS Cancer molecular profiling suite.
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AASLD 2019

With NASH drugs on cusp of arrival, noninvasive diagnostics are the 'second pillar of need'

Nov. 12, 2019
By Anette Breindl
BOSTON – For diagnosing nonalcoholic steatohepatitis (NASH), liver biopsy is "the reference standard," Dean Hum, president of Genfit Corp., told BioWorld MedTech. "I'm not going to call it the gold standard."
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BioWorld MedTech's Diagnostics Extra

Nov. 8, 2019
Keeping you up to date on recent developments in diagnostics.
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AI the future of collapsed lung diagnosis, says Ontario lab

Nov. 8, 2019
By David Godkin
TORONTO – On average, radiology specialists diagnose fewer than 50% of cases of collapsed lung or pneumothorax using chest X-rays, said systems design engineer Hamid Tizhoosh. The Insignio system developed at Tizhoosh's Kitchener, Ontario-based Kimia Lab has gone further by identifying 75% of cases of collapsed lungs using artificial intelligence (AI) to search a database of 550,000 patients and compare 30,000 cases of pneumothorax there to X-rays of new patients with unknown conditions.
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DNA illustration

FDA authorizes first NGS test to detect critical HIV-1 drug resistance mutations

Nov. 7, 2019
By Meg Bryant
Singapore-based Vela Diagnostics Holding Pte. Ltd. has received U.S. FDA authorization via the de novo approval pathway for an in vitro diagnostic test to detect HIV-1 genomic drug resistance mutations (DRMs). The Sentosa SQ HIV-1 Genotyping Assay – the first HIV-1 genotyping next-generation sequencing (NGS) assay to win an FDA nod – uses plasma of patients infected with HIV-1 to detect HIV-1 Group M DRMs in the protease, reverse transcriptase and integrase regions of the pol gene in a single test.
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Genetic-Signature-product-line

Genetic Signatures ready to go global with AU$35M raise

Nov. 6, 2019
By Tamra Sami
PERTH, Australia – Sydney-based molecular diagnostics company Genetic Signatures Ltd. is poised to extend its global footprint to the U.S. and Europe following its AU$35 million (US$24 million) capital raise.
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Sulfide stress as new target?

Schizophrenia biomarker can be detected in human hair

Nov. 5, 2019
By John Fox
A subtype of schizophrenia is related to abnormally high brain levels of hydrogen sulfide (H2S), which has important implications for the development of new treatments, according to a study by researchers at the RIKEN Center for Brain Science (CBS) in Japan.
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BioWorld MedTech's Diagnostics Extra

Nov. 1, 2019
By Holland Johnson
Keeping you up to date on recent developments in diagnostics.
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Myriade launches optical instrument that visualizes viruses in real time

Nov. 1, 2019
By Bernard Banga
PARIS – Myriade SAS reported the commercial launch of its Videodrop technology at the second congress of the French Society of Extracellular Vesicles (FSEV) held in October in Nantes. This new nanoscale imaging technique captures all nanoparticles ranging from 30 nm to 10 μm in a droplet of solution (5-10μl volume), without initial data labeling.
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