Rosetta acquired PersonalizeDx and its range of molecular diagnostic offerings in early 2015 for $2 million in cash plus stock.
The test, miRpredX 31-3p, is a positive theranostic test that quantifies the expression of miR-31-3p in FFPE using RT-qPCR technology.
The grants include awards for projects using genetics to identify differences in how ASD affects boys versus girls, and how to improve treatments.
A new genome sequence study suggests sequence conservation is more common in HPV16 isolates from individuals with cancer or pre-cancerous conditions.
The bill, which was approved by a Senate subcommittee yesterday, would increase the National Institutes of Health's fiscal 2018 budget to $36.1 billion.
Variants in and around inflammation-related gene CD53 were linked to TB in older Thai individuals infected with certain Mycobacterium tuberculosis lineages.
The two projects aim to use genomics to prevent the spread of drug-resistant bacteria and expand the use of genomic testing in cancer, respectively.
The firm reported an 88 percent increase in product sales, but this was offset by a 79 percent drop in collaboration revenues.
Illumina has filed a new lawsuit against Premaitha, claiming it infringes on an Illumina patent related to noninvasive prenatal testing.
A new genome-wide association study involving data from thousands of 23andMe customers implicated six loci in gestational duration or preterm birth risk.
The firm plans to launch its first test from the lab, a mRNA-based noninvasive confirmatory lung diagnostic, by the end of this year.
With the cash, WuXi NextCode will build out its AI and deep learning, seek partnerships in precision medicine and diagnostics, and commercialize genomic tests.
The firm said it intends to use net proceeds from the issuance of the notes for general corporate purposes.
More than a dozen Yersinia pestis sub-populations turned up in a genome sequence and genotype analysis of strains collected across the country over 18 years.
The bill would increase the NIH's fiscal 2018 budget to $36.1 billion — $2 billion more than the agency was allocated in the prior fiscal year.
FDNA's technology uses facial analysis, deep learning, and artificial intelligence to evaluate symptoms of patients with rare genetic diseases.
British genomics interpretation software vendor Congenica inked a deal with a Portuguese hospital to analyze whole-exome sequencing data for the In2Genome project.
Sanbio, a Netherlands-based distributor that serves the Belgium, the Netherlands, and Luxembourg, will distribute Canon's Novallele assays and controls.
Researchers from MSKCC reported today in JAMA that of 1,040 cancer patients referred for germline mutation testing, 18 percent had actionable variants.
The researchers believe that the discovery of the genetic loci linked to T2D and CHD will lead to therapeutic opportunities to lower the risk of both diseases.
The companies will validate and commercialize the assay as a companion diagnostic to identify best responders to Morphotek's investigational ovarian cancer treatment.
The company said it will use the proceeds from the offering for working capital and general corporate purposes, among other things.
Medcis Pathlabs and its associates and attendees will buy Co-Diagnostics' tests for hepatitis B, hepatitis C, HIV, and human papillomavirus.
The company said that more than 95 percent of eligible early-stage breast cancer patients can now have the test paid by insurance.
The panel, developed by collaborator Janssen, is expected to improve detection of influenza and respiratory syncytial virus.
Two researchers have found that behavioral genetic defenses in criminal cases don't tend to affect outcomes, according to Popular Science.
Researchers report that while host genetics influence the oral microbiome, they don't appear to affect cavity-causing microbes, the Economist says.
Pandas' gut microbiomes change as what they eat changes with the seasons, writes Discover's Inkfish blog.
In PLOS this week: comparative genomic study of malaria-linked macaque parasite, search for apple root reference genes, and more.