translational genomics South Carolina Population Genomics Program Marks First Anniversary With Surge in Participation Premium The In Our DNA SC partnership between MUSC and Helix is still struggling to match the diversity of the South Carolina population, but outreach is expanding. AnFiSA Developers Ready Open-Source Analysis Software for Simultaneous Research, Clinical Use Premium The "fully open-source" variant curation application is meant to support translational multiomics and improve rare-disease diagnostics. Single-Nucleus Sequencing Holds High Risk, High Reward for Translational Transcriptomics Premium As researchers embrace single-nucleus analysis to probe previously intractable tissues, companies are trying to deliver more reliable sample preparation. Melbourne Genomics Health Alliance to Receive A$36M in New Government Funding The alliance of hospitals, research groups, and academic institutes is tasked with implementing clinical genomics programs in Australia's state of Victoria. Parents, Physicians View Genome Sequencing as Useful for Managing Care of Seriously Ill Infants NSIGHT2 researchers surveyed the parents and doctors of sick babies to see how useful they found positive and negative findings from genome sequencing tests. Aug 11, 2020 NanoString Launches NGS Readout for Spatial Transcriptomics, Partners With Illumina on Informatics Premium Feb 25, 2020 ReadCoor Launches Spatial Multiomics Platform at AGBT Premium Feb 25, 2020 10x Genomics Unveils 2020 New Product Pipeline at AGBT Premium Dec 4, 2019 Pilot GenomeAsia 100K Project Highlights Insights Gleaned From Diverse Dataset Dec 2, 2019 Columbia Study Finds Low Patient Engagement With Basic Genomic Education Videos Premium Dec 2, 2019 Fujitsu Laboratories, Aichi Cancer Center to Develop AI-Based Tech for Cancer Genome Data Analysis Nov 18, 2019 Mount Sinai Using $2M NIH Grant to Build New Supercomputer for Omics Research Nov 14, 2019 Gene Screen Leads to Potential Malaria Targets in Liver-Stage Plasmodium Parasites Nov 13, 2019 ACMG, ClinGen Publish Recommendations for Interpretation, Reporting of CNVs Nov 12, 2019 NorthBay Healthcare to Pilot GenomeSmart Genetic Test Recommendation Platform Nov 12, 2019 AMP Attendees Reflect on Uptake of Tumor Mutational Burden Amid Validation, Utility Questions Premium Nov 12, 2019 India's IndiGen Project to Sequence 20K Genomes, Support New Clinical Applications Premium Nov 11, 2019 Chatbots Could Help Human Genetic Counselors Focus on Patient Concerns Nov 7, 2019 Hitachi, French Cancer Center Partner on AI-Focused Research Nov 6, 2019 U of Vermont Health Network Launches DNA Risk Screening Pilot Program Nov 6, 2019 Jax, Microsoft Team to Mine Medical Literature for Curating Clinical Knowledgebase Premium Nov 5, 2019 CIViC Developers Enhancing Variant Database for Greater Use in Precision Oncology Premium Nov 4, 2019 Ovarian Cancer Omics Consortium Receives $500K DoD Grant for Early Detection Biomarker Discovery Nov 4, 2019 Early-Onset Alzheimer's Mutation May Be Mitigated by APOE Variant Oct 31, 2019 HER2 Amplification Confers Drug Sensitivity Across Tumor Types in New Study Premium Load More Breaking News New Products Posted to GenomeWeb: Qiagen, Thermo Fisher, Bionano Genomics, BillionToOne, More People in the News at Illumina Ventures, Element Biosciences, Epigenomics, Exagen, More Genomic Approaches Boost Rare Disease Diagnoses in Middle Eastern Patient Population GeneDx to Raise $150M in Public and Direct Stock Offerings In Brief This Week: T2 Biosystems, Novacyt, OpGen, Dante Genomics, Nautilus Biotechnology, More The Scan Self-Reported Hearing Loss in Older Adults Begins Very Early in Life, Study Says A JAMA Otolaryngology — Head & Neck Surgery study says polygenic risk scores associated with hearing loss in older adults is also associated with hearing decline in younger groups. Genome-Wide Analysis Sheds Light on Genetics of ADHD A genome-wide association study meta-analysis of attention-deficit hyperactivity disorder appearing in Nature Genetics links 76 genes to risk of having the disorder. MicroRNA Cotargeting Linked to Lupus A mouse-based study appearing in BMC Biology implicates two microRNAs with overlapping target sites in lupus. Enzyme Involved in Lipid Metabolism Linked to Mutational Signatures In Nature Genetics, a Wellcome Sanger Institute-led team found that APOBEC1 may contribute to the development of the SBS2 and SBS13 mutational signatures in the small intestine.