data-management software Geneial Proposes Marketplace Approach to Rare Disease Data Sharing Premium Geneial's cofounders want to create a platform where drug developers, CROs, and others studying rare genetic diseases can buy biomedical data. LatchBio Touts 'No-Code' App Development in Multiomic Analysis Premium Started by three UC Berkeley dropouts and fresh off a $28 million Series A, LatchBio seeks to bridge the gap between biologists and bioinformaticians with its software ecosystem. Lifebit to Build 'Trusted Research Environment' for Danish National Genome Center The UK-based biotech firm signed a four-year contract to deploy its CloudOS software in support of the Danish program to sequence 60,000 genomes by 2024. Lifebit, Boehringer Ingelheim Collaborate on Data, Analytics for Drug Discovery Lifebit Biotech will help Boehringer Ingelheim build a scaleable clinicogenomics data platform in the cloud. Lifebit Counting on New UK Partnerships to Develop, Validate Federated Data Model Premium Lifebit is helping the Cambridge Biomedical Research Centre build a "trusted research environment" that could serve as a global model for genomic data sharing. Feb 1, 2022 Zetta Genomics Raises £2.5M in Seed Funding Oct 22, 2021 Pfizer Centralizes RNA-seq Data on Seven Bridges Under Integrative Biology Program Premium Oct 20, 2021 Amazon Genomics CLI Seeks to Improve Integration of Bioinformatics With AWS Cloud Premium Sep 29, 2021 Lifebit Biotech Closes $60M Series B Funding Round Sep 7, 2021 Seqera Labs Raises $5.5M in Seed Funding Jun 14, 2021 Celemics, Strand Life Sciences Partner on Integrated Platform for NGS Analysis Apr 23, 2021 WANdisco Moves Into Genomics With Korean Data Deal Premium Apr 20, 2021 GenomSys Gets CE Mark for MPEG-G Codec Genomic Data Processing Software Suite Apr 15, 2021 Rosalind Partners with Geninus, Helixrus to Bring Single-Cell Software to Asian Markets Mar 25, 2021 Sophia Genetics, Hitachi Partner on Data-Driven Precision Medicine Mar 22, 2021 Insightful Science to Acquire Dotmatics Feb 2, 2021 Congenica, Gabriel Precision Oncology Partner on Clinical Interpretation for Somatic Cancer Testing Feb 2, 2021 Syapse Raises $68M in Equity Financing Jan 14, 2021 GeneInfoSec Wants Genetic Data Security to Start at Molecular Level Premium Jan 4, 2021 Enpicom Sees Personalized Medicine Coming Into Focus After Busy 2020 Premium Dec 15, 2020 Life Sciences Software Company Nference Completes $60M Series C Funding Round Dec 15, 2020 Enpicom, MiLaboratories Partner on Immune Repertoire Sequencing Software Integration Oct 27, 2020 OmniTier Introduces Appliance for Tertiary Next-Generation Sequencing Analysis Premium Sep 25, 2020 M2Gen Expands Partnership With Discovery Life Sciences Sep 21, 2020 Nebula Genomics, Oasis Labs Partner to Offer Secure Personal Genomic Data Load More Breaking News Simple HealthKit Raises $8M in Series A Round Top Five Articles on GenomeWeb Last Week: Quantum-Si Layoffs, UBS Coverage Initiations, More LumiraDx Secures FDA Emergency Use Authorization, UK Approval for COVID-19, Flu Test Rarity Bioscience Raises Additional €500,000 Cancer Prognoses Informed by Module-Based Approach, Study Finds The Scan UK Team Presents Genetic, Epigenetic Sequencing Method Using enzymatic DNA preparation steps, researchers in Nature Biotechnology develop a strategy for sequencing DNA, along with 5-methylcytosine and 5-hydroxymethylcytosine, on existing sequencers. DNA Biobank Developed for French Kidney Donors, Recipients The KiT-GENIE biobank described in the European Journal of Human Genetics contains DNA samples, genotyping profiles, immune patterns, and clinical features for thousands of kidney donors or transplant recipients in Nantes, France. Cardiometabolic Disease May Have Distinct Associations With Microbial Metabolites in Blood, Gut By analyzing gut microbes in combination with related metabolites in feces and blood, researchers in Nature Communications found distinct cardiometabolic disease relationships at each site. Study Reveals New Details About Genetics of Major Cause of Female Infertility Researchers in Nature Medicine conducted a whole-exome sequencing study of mote than a thousand patients with premature ovarian insufficiency.