NEW YORK (GenomeWeb News) – The National Human Genome Research Institute today launched the first version of a free, online toolkit of phenotypic data.

NHGRI said that the resource is aimed at standardizing measurements of research subjects' physical characteristics and environmental exposures. It said that the toolkit will provide researchers with more power to compare data across multiple studies, which will accelerate efforts to understand the complex genetic and environmental factors that cause cancer, heart disease, depression, and other common diseases.

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UCSF researchers find that having two X chromosomes may contribute to women's longer lifespans, according to Discover's D-brief blog.

In PNAS this week: immune cell profiling of wild baboons by social status, metabolomics profiling of esophageal tumors, and more.

A genomic analysis of modern and ancient maize reveals a complicated domestication history, according to Reuters.

In PLOS this week: MYRF variant linked to congenital diaphragmatic hernia, analysis of the "dragon's blood" red resin produced by traditional medicine plants, and more.

Jan
30
Sponsored by
Loop Genomics

This webinar will provide a comparison of several next-generation sequencing (NGS) approaches — including short-read 16S, whole-genome sequencing (WGS), and synthetic long-read sequencing technology — for use in microbiome research studies.

Jan
30
Sponsored by
Loop Genomics

This webinar will provide a comparison of several next-generation sequencing (NGS) approaches — including short-read 16S, whole-genome sequencing (WGS), and synthetic long-read sequencing technology — for use in microbiome research studies.