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Watching CRISPR
The Los Angeles Times says CRISPR gene editing is a field to watch in the next year.
For the Owls and Larks
Researchers are developing blood tests to determine people's chronotypes, according to Scientific American.
New Mice for the Job
Researchers have developed a new Alzheimer's disease mouse model with greater genetic diversity.
Resolution Bioscience Holds Focus on Liquid Biopsy CDx, Kit Development as it Preps for Growth
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The firm is moving into a larger facility after its first full year of profitability and planning new hires to support its plans to bring liquid biopsy kits through the FDA.
Sequencing Historical, Modern Gorilla Genomes Uncovers Genetic Ramifications of Population Decline
Modern Grauer's gorillas have experienced a decline in genetic diversity, more so than mountain gorillas, even as both have experienced population decline.
Epigenomics Pushes New Promotion Efforts for ProColon Test as Other Assays in Pipeline Advance
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The firm has struggled in the past to convince payors of its test's clinical utility but remains dedicated to convincing the field that Epi proColon can help patients by closing CRC screening gaps.
Sink-Scrubbing Time
A sequencing-based analysis of sphingomonas infections at the National Institute of Health's Clinical Center traced them to patient sinks, Stat News reports.
Converso Ancestry Uncovered
A genetic analysis has uncovered what appears to be Converso ancestry among a large cohort of Latin American individuals, Forbes reports.
Search for Risk
A University College London team aims to examine genetic and other factors influencing eating disorder risk, according to the Guardian.
US District Court Sides With Roche, Ariosa in NIPT Patent Case Filed by Illumina
The court cited previous US Supreme Court rulings, including Mayo vs. Prometheus, in determining that certain claims of Illumina's patents were invalid.
The research highlighted particular challenges for gram-negative organisms among a population of higher-risk patients.
Foundation Medicine Cancer CDx Approved in Japan
Foundation Medicine's assay detects genomic alterations in 324 cancer genes and serves as a companion diagnostic for patients with certain types of tumors.
Diverse Chronic Kidney Disease Diagnoses Made With Exome Sequencing
A new analysis found kidney disease-related pathogenic or likely pathogenic variants in exomes for roughly 9 percent of individuals with chronic kidney disease.
Doing OK
The Guardian reports that biotech in the UK has been reaping investments despite the upcoming Brexit.
Closed, Again
The partial federal government shutdown in the US affects a number of science agencies, ScienceInsider reports.
Back for More Testing
The Associated Press reports California governor Jerry Brown has ordered new DNA tests in a 35-year-old quadruple murder case.
This Week in Genome Biology: Dec 26, 2018
In Genome Biology this week: catalog of curated human genes and transcripts; potential biomarkers for aging; and more.
GenMark Fungal Blood Culture Test Clears FDA
The test is the second of three panels intended to detect pathogens that cause the bloodstream infections that can lead to sepsis.
Novo Nordisk to Invest $150M in Danish National Genome Center
The funds will provide financial support to the genome center's data and information technology unit beginning next year.
Major EHR vendor Cerner would like to see the SMART on FHIR protocol take off as it seeks to make genomic data just another element of a patient's record.
Personalized Medicine 2018: More Drugs, Greater NGS Adoption, Growing Appreciation of Dx Value
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New drugs, tests, and policies suggest steady and continued future growth in the space, though public awareness of personalized medicine continues to lag.
Brad Wertz
Brad Wertz, chairman and founding investor of GenomOncology, will take over as CEO on Jan. 1, the Cleveland-based company announced. Manuel Glynias, GenomOncology's current CEO and founder, will remain president. Wertz has a history of scaling technology companies in various industries as they move from startup to growth phase, including bioinformatics software maker Acero.
Pediatric Genetic Disease Contributes Disproportionately to Healthcare Costs
The analysis found that charges for suspected genetic diseases account for between 11 percent and 46 percent of pediatric healthcare costs in the US.
Sequencing Could Screen for Mendelian Disorders, Aneuploidy in Preimplantation Genetic Testing
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Researchers tested the combined PGS and PGD assay in a pilot study and now aim to validate it on larger numbers of disorders and compare it to conventional testing.