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In Brief This Week: Quest Diagnostics; Rosetta Genomics; GeneNews

NEW YORK (GenomeWeb News) – Quest Diagnostics this week said that its Simplexa Flu A/B & RSV Direct test has received the CE Mark and has been launched in Europe. The molecular test, developed by the firm's Focus Diagnostics business, runs on the 3M Integrated Cycler. The test uses a proprietary technique to eliminate nucleic-acid sample extraction, leading to faster results reporting, said Quest.


Rosetta Genomics has raised $1.5 million of its planned $1.9 million target in a private placement, according to documents filed with the US Securities and Exchange Commission. Last month the firm said that it had reached definitive agreements to place the common stock and warrants with investors.


GeneNews this week said that its shareholders have approved the proposed consolidation of the firm's issued and outstanding shares on the basis of one post-consolidation common share for every six pre-consolidation common shares. The Canadian molecular diagnostics firm has not set a definitive date for the reverse split, but said that it would take place no later than Jan. 31, 2012.

"We believe that this proposed share consolidation will provide shareholders with the potential for a more attractive share price, reduced shareholder transaction costs, and improved trading liquidity as our partners prepare to launch ColonSentry in their respective markets," GeneNews President and COO Gailina Liew said in a statement.

The Scan

Response Too Slow, Cautious

A new report criticizes the global response to the threat of the COVID-19 pandemic, Nature News reports.

Pushed a Bit Later

Novavax has pushed back its timeline for filing for authorization for its SARS-CoV-2 vaccine, according to Bloomberg.

AMA Announces Anti-Racism Effort

The Associated Press reports that the American Medical Association has released a plan to address systemic racism in healthcare.

Nucleic Acids Research Papers on miRMaster 2.0, MutationTaster2021, LipidSuite

In Nucleic Acids Research this week: tool to examine small non-coding RNAs, approach to predict ramifications of DNA variants, and more.