Illumina, University of Copenhagen to Study Genetic Evolution of Neuropsychiatric Disease

Mar 26, 2019

|

NEW YORK (GenomeWeb) – Illumina said today that it is working with the Lundbeck Foundation GeoGenetics Centre at the University of Copenhagen to study how infectious pathogens influenced the evolutionary history of certain mental and neurological disorders.

To read the full story....

...and receive Daily News bulletins.

Already have a GenomeWeb or 360Dx account?
Login Now.

Don't have a GenomeWeb or 360Dx account?
Register for Free.

Breaking News

The Scan

Viral Genomes Back in Time

Researchers uncovered the HIV virus within a tissue sample collected in 1966, the Atlantic reports.

To Give a Microbiome?

Nature News reports there are a handful of clinical trials underway to evaluate vaginal microbiome seeding of newborns born via caesarian section.

The End of the Cave Bears

The Washington Post writes that humans may have contributed to the extinction of cave bears some 20,000 years ago.

PLOS Papers Tackle Trypanosomiasis Susceptibility, Diabetes Modulators, More

In PLOS this week: gene variant may protect against trypanosomiasis, GLIS3 role in type 2 diabetes, and more.

Featured White Papers

A High-Performance Solution Combining CleanPlex OncoZoom Cancer Hotspot Panel and SOPHiA AI for Rapid Characterization of Somatic Mutations

Automated Genomic DNA Extraction from Large Volume Whole Blood

Automated Library Preparation for the MCI Advantage Cancer Panel Utilizing the Beckman Coulter Biomek i5 Span-8 NGS Workstation

Correlation Between Mutations Found in FFPE Tumor Tissue and Paired cfDNA Samples

Aug

22

Featured Webinar

Biobanks and the Rise of Precision Medicine: Lessons from the Estonian Biobank

This webinar will discuss how the Estonian Biobank, a cohort of more than 165,000 participants, is addressing industry challenges with data management and collaboration in the transition to precision medicine.

Aug

29

Featured Webinar

Biobanking at Scale to Support Precision Medicine

This webinar will outline how RUCDR Infinite Biologics, the world's largest university-based biorepository, has implemented workflows and processes to support precision medicine applications.

Sep

18

Featured Webinar

Highly Sensitive Structural Variant Detection for Medical Genetics: A Comparison to the Standard of Care

This webinar will outline how a team at Radboud University Medical Center is assessing ultra-long read optical mapping on the Bionano Saphyr system to replace classical cytogenetics approaches in routine testing and for the discovery of novel structural variants with potential scientific, prognostic, or therapeutic value that are missed by standard approaches.

Oct

23

Featured Webinar

Single-Cell Methylation Profiling of Pediatric Tumors via a Unique NGS-based Approach

This webinar will illustrate how single-cell methylation sequencing can be applied to gain significant insight into epigenetic heterogeneity in disease states, advancing cancer research discoveries.

Menu