Using point mutation and structural variant patterns in 133 ovarian cancer cases, researchers identified seven clusters to classify the disease and predict patient outcomes.
The consortium is collecting data from different omics streams for a cohort of individuals with autism spectrum disorders with the long-term goal of improving treatment.
In Nature this week: studies of prostate cancer aggressiveness, and more.
The method allows analysis of copy number at the individual cell level with greater coverage uniformity and more reliable detection than other approaches.
The researchers will use genomics to address challenges facing Canada's forestry, healthcare, agricultural, and aquacultural industries.
The Canadian company recently published results of a study demonstrating the utility of its pharmacogenomic testing and decision support platform.
Researchers demonstrated that Strand-seq directional single-cell sequencing can be used to assemble consensus chromosome haplotypes for an individual.
The research team linked a mutation in a protein-coding gene to inherited multiple sclerosis and genetic risk factors for developing the disease.
The researchers used whole-genome and single-cell sequencing to study cell migration patterns and clonal diversity, using new single-cell genotyping software.
Researchers diagnosed almost 70 percent of the neurometabolic cases they tackled, using exome sequence data for dozens of affected children and their families.
According to NPR, an antibody-based test could identify people who were exposed to SARS-CoV-2 and either didn't develop symptoms or were misdiagnosed.
A sequencing analysis of New York City rats indicates they have adapted to the urban environment there, according to a recent preprint.
Ars Technica reports that a multicellular eukaryotic parasite has lost its mitochondria.
In Science this week: perspective piece says AI can accelerate drug discovery by using genomic and chemical data, and more.