Researchers narrowed in on a HMGA2 gene haplotype that became more common in small-beaked medium ground finches competing for food during a drought.
A University of Pittsburgh research team used a novel computational approach to uncover the protein interactions, which may be potential treatment targets.
The FDA, journals, and even payors are encouraging labs to deposit variant data in public databases, but collaboration is needed to resolve interpretation discrepancies.
Sanger Institute researchers analyzed the genomes and mutational signatures of 560 breast cancer tumors, identifying new ways to classify the disease.
Questions remain about how the €6.7 billion ($7.6 billion) pledged for the implementation of the European Open Science Cloud over the next four years will be spent.
The certification enables the company's lab in Grenoble to receive patient specimens from the US for testing with its ImmuneTracker Dx cancer immunotherapy assay.
DeCode Genetics' Kari Stefansson and his colleagues uncovered a dozen genetic variants that influence blood lipids, and explored links to coronary artery disease.
Partnering with Biodist Group, the South Korean molecular diagnostics firm is looking to move into non-human applications such as food safety testing.
In PLOS this week: founder mutation linked to some leukoencephalopathy cases, transcript and protein profiles of the kissing bug, and more.
BGI CEO Ye Yin says that mapping variation within the human genome will bring a "big data revolution" to healthcare, Wired UK writes.
All the images that investigators produce through their research present a challenge to share, Nature News reports.
The House of Representatives science committee has approved a measure that includes new rules for large National Science Foundation projects, ScienceInsider reports.
This webinar highlights important features and demonstrates the practical aspects of using the NCBI BLAST service.
This on-demand webinar demonstrates how automated liquid handling workstations can reduce bottlenecks in library preparation for next-generation sequencing, enabling scientific advances in genomics research that were not possible five years ago.
This online seminar demonstrates how RNA-seq analysis in a model organism can provide insights into human disease.