A UCSD research team looked at whole-genome sequencing data for breast cancer patients to better understand kataegis and cancer prognosis.
TheSTARPlatform includes tools for analyzing genomic data from raw sequence through to variants calls as well as for compressing and storing data.
The laboratory will employ dedicated computational biologists and bioinformaticians to analyze genomic datasets for ALSF-funded researchers and other scientists.
Consortium researchers will use the STARPlatform to manage whole exome and genome sequence from patients with three diffuse glioma subtypes.
The portal offers access to genotype, phenotype, and clinical data related to type 2 diabetes as well as computational tools for querying the information.
The supercomputer was used to identify genomic variants in some 300 deeply sequenced human samples for use in a planned bead-array-based genotyping chip.
Two research teams found potentially useful PGx variants in more than 1,000 participants in the NIH Undiagnosed Diseases Program, as well as in a handful of ClinSeq participants.
The web-based gene analysis software is now implemented on IU's NCGAS resources and will soon be running on hardware at other XSEDE network sites.
The company said its new genetic variation analysis and visualization system will help provide clinicians with a more efficient way to make decisions about patient care.
The companies plan to combine Macrogen's sequencing capabilities with Systems Imagination's analysis tools.
NPR reports that the patient who underwent a CRISPR-based treatment for sickle cell disease is doing well.
Resistance to ash dieback disease among some UK ash trees appears polygenic, the Independent reports.
In Nucleic Acids Research this week: sequencing strategy for flash-frozen brain tissue bank samples, new version of ChlamDB, and more.
A UK woman is suing three National Health Service Trusts for not telling her about her father's Huntington's disease diagnosis, the BBC reports.