CNV arrays Study Finds Copy Number Variant Ties to Complex Human Traits Data for 331,522 UK Biobank participants helped link CNVs to dozens of complex human traits and uncover pleiotropic, heterogeneous, and polygenic CNV effects. Oxford Gene Technology Expands NGS Offering Into Constitutional Cytogenetics Premium The company believes cytogeneticists will adopt its panel to get high-quality SNV and CNV data in a single assay. Non-Small Cell Lung Cancer Mutations, Tumor Microenvironment Profiled in China Researchers identified characteristic alterations, immune features, and interactions in hundreds of adenocarcinoma and squamous cell carcinomas from China. Novel CNVs Uncovered Affecting Genes Involved in Drug Metabolism An international team of researchers examined the scope and population specificity of copy-number variants affecting genes linked to drug metabolism. New Schizophrenia-Associated CNVs Unearthed in Large Psychiatric Genomics Consortium Study Using CNV profiles for more than 40,000 individuals with or without schizophrenia, researchers got a refined look at gains and losses linked to the condition. Sep 14, 2016 New Congenital Heart Disease CNVs Reported in Chinese Population Nov 9, 2015 Sézary Syndrome Studies Describe Recurrent Mutations in Leukemic Condition Aug 15, 2012 Copy Number Analyses ID Gene Tied to Treatment Resistance in Ovarian Cancer Oct 19, 2011 BGI Collaborates with Autism Group to Sequence 10K Genomes with Eye Toward Diagnosis, New Treatments Premium Apr 6, 2010 Research Teams Catalog and Characterize CNVs Mar 31, 2010 WTCCC Data Suggests Common CNVs Not Key Common Disease Culprits Oct 7, 2009 International Team Characterizes Common Human CNVs Breaking News Ceres Nanosciences Wins $1.4M in NIH RADx Funding for Additional Wastewater Epidemiology Centers Study Unearths Features Found in Long-Term Survivors of Advanced Ovarian Cancer GenomeWeb Top 40 up 8 Percent in November, Outpacing Broader Market Oxford Nanopore Technologies, Bio-Techne Partner to Develop Carrier Screening Assay ERS Genomics Licenses CRISPR-Cas9 IP to Cosmo Bio The Scan New Study Investigates Genomics of Fanconi Anemia Repair Pathway in Cancer A Rockefeller University team reports in Nature that FA repair deficiency leads to structural variants that can contribute to genomic instability. Study Reveals Potential Sex-Specific Role for Noncoding RNA in Depression A long, noncoding RNA called FEDORA appears to be a sex-specific regulator of major depressive disorder, affecting more women, researchers report in Science Advances. New mRNA Vaccines Offer Hope for Fighting Malaria A George Washington University-led team has developed mRNA vaccines for malaria that appear to provide protection in mice, as they report in NPJ Vaccines. Unique Germline Variants Found Among Black Prostate Cancer Patients Through an exome sequencing study appearing in JCO Precision Oncology, researchers have found unique pathogenic or likely pathogenic variants within a cohort of Black prostate cancer patients.