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NEW YORK ─ Luminex said on Monday that it has received a warning letter from the US Food and Drug Administration related to operations in its Austin, Texas, and Northbrook, Illinois, facilities and its Verigene Processor SP System.

In a document filed with the US Securities and Exchange Commission, the firm said that the warning letter results from inspections held at the facilities from Feb. 10, 2020 to Feb. 14, 2020, and that it pertains to FDA requirements for the Verigene SP instrument and its hybridization heater.

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Science reports that a new White House Office of Management and Budget memo rescinds previous ones that helped research institutions deal with pandemic-related closures.

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In Genome Research this week: Y chromosome gene expression analysis, de novo mutations rise with paternal age in rhesus macaques, and more.

Jul
14
Sponsored by
Agilent

This webinar will describe a rapid metagenomics assay under development for human pathogens, including the SARS-CoV-2 coronavirus.

Jul
16
Sponsored by
NanoString

Join this webinar to learn how spatial resolution of gene expression in tumor tissue reveals new insights in biomarker discovery and therapeutic response. 

Aug
13
Sponsored by
10x Genomics

This webinar will discuss a study that combined single-cell gene expression and spatial gene expression to understand the evolution of sepsis in the kidney at the cellular and molecular level.