Microarrays & Multiplexing

News on microarrays, multiplexing, genotyping, cytogenetics, gene expression profiling in genetics, genomics, and molecular diagnostics.

NanoView Inks Japanese Distribution Deal for Exosome Characterization System

The recently launched system can measure the concentration and size of extracellular vesicles as small as 50 nanometers and requires no sample preparation.

Cell Microsystems Awarded $1.6M NIH Grant for Single Cell Analysis

The firm will work with investigators from the University of North Carolina at Chapel Hill and the University of Virginia to validate its AIR system in CRISPR workflows.

Prescient Medicine Acquires AutoGenomics

Prescient will further the development and commercialization of the Infiniti Neural Response Panel to identify patients who may be at risk for opioid use disorder.

WINTHER Trial Highlights Challenges, Potential of Transcriptomics for Precision Oncology

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While the study didn't meet its primary endpoint, it showed the potential of transcriptomics to match cancer patients to beneficial treatments.

Enzo, Hologic, Grifols Settle Patent Dispute

Under the terms of the settlement, Enzo Life Sciences will receive $14 million in exchange for granting global licenses to Hologic and Grifols.

Apr 15, 2019

GenMark Diagnostics Obtains FDA Clearance for Gram-Negative Sepsis Panel

Apr 11, 2019

Hirschsprung's Disease Genetic Analysis Reveals Mix of Common, Rare Risk Variants

Apr 01, 2019

First Epigenetic Signature Test for Inherited Disorders to Launch in the US, Europe

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Mar 28, 2019

MiR Scientific Prepares to Launch Tests for Prostate, Bladder Cancer

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Mar 28, 2019

NanoString, Bio-Techne to Codevelop, Market Integrated RNA Spatial Profiling Workflow

Mar 25, 2019

Leukemia Relapse After Stem Cell Transplant Linked to Transcriptional Signature

Mar 22, 2019

Cannabis Testing Labs Adopt Molecular Methods as Throughput, Sample Diversity Skyrocket

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Mar 15, 2019

Opioid Dependence Linked to Decreased Methylation in Several Genes

Mar 11, 2019

Researchers Identify Potential Causal Variants Linked to Blood Cell Traits

Mar 08, 2019

Frontal Fibrosing Alopecia GWAS Implicates Risk Loci with Links to Immune System

Mar 05, 2019

Carpal Tunnel GWAS Highlights Growth-Related Loci, Genetic Ties to Height

Mar 05, 2019

Canker Sore Risk Influenced by Nearly 100 Genetic Variants, GWAS Reports

Feb 28, 2019

Alzheimer's Disease Meta-Analysis Identifies Five New Risk Genes

Feb 26, 2019

New IBD Adverse Drug Response Risk Gene Identified

Feb 26, 2019

COPD Genome-Wide Association Study Reveals Numerous Risk Variants

Feb 25, 2019

Insomnia Studies Reveal New Risk Loci, Related Conditions

Feb 25, 2019

Autism Spectrum Disorder GWAS Highlights Common Risk Variants, Overlap With Other Conditions

Feb 22, 2019

Asthma-Linked Loci Uncovered in Genome-Wide Analysis of Individuals of African Ancestry

Feb 13, 2019

Diabetes Genetic Risk Assay Shows Improvement, Investigators Plan IVD Kits

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Feb 08, 2019

Genetic Genealogy Firms Reassure Clients About Data Privacy After FTDNA Divulges FBI Partnership

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The Scan

Bill to Ease Post-Conviction DNA Testing Access

The Oregon state Senate unanimously passed a bill that would make it easier for people convicted of crimes to initiate DNA testing of evidence, according to the Associated Press.

Ah, Feel Full Now

People reports that researchers have uncovered genetic variants that lead people to always feel full.

Life Insurers, Too, in Florida?

Florida state senators are to weigh a bill prohibiting life insurance companies from using genetic information in coverage decisions, according to Florida Politics.

This Week in Genome Research

In Genome Research this week: metagenomic sequencing assay that detects pathogens in cerebrospinal fluid, single-tube long fragment read approach, and more.

Featured White Papers

Controlling Ribonuclease (RNase) with High Irradiance UV LED Light Engines

Optimized NGS Library Preparation with Acoustic Liquid Handling

May

15

Featured Webinar

Discovery of Exon-Level CNVs in Daily Practice for Constitutional Genome Testing

This webinar will discuss how Radboud University Medical Center’s Department of Human Genetics is using exon-level copy number variant (CNV) detection by microarray to assist its efforts in constitutional genome testing.

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