Elsevier NIH Awards $9M in Funding to Support Data Commons Pilot Phase Participants in the pilot will begin developing the capabilities required for the planned data commons, including making data transparent and interoperable. SolveBio, Elsevier Ink Product Integration Pact The companies will integrate Elsevier's database of biological molecular interactions and curated pathways with the SolveBio operation system for molecular information. SoftGenetics, Elsevier Sign Software Integration Deal The integrated products will provide a seamless workflow for interpreting next-generation sequence data from alignment through pathway analysis. Elsevier Continues Focus on Pharmacovigilance, Updates Sequence Analysis Software Premium The company is working on a bespoke pharmacovigilance product that will leverage its biomedical content, and has added an NGS module to Pathway Studio. Elsevier, Maverix Ink Software Integration Agreement Under the terms of the agreement, the companies will combine software products and data to improve NGS analysis and interpretation Jun 27, 2014 Downloads and Upgrades: GenomeQuest IP Management Module, Blast on AWS, and More Premium May 30, 2014 Elsevier Combines Resources to Improve Drug Adverse Event Monitoring for Pharma Premium Apr 18, 2014 Downloads and Upgrades: Elsevier's Reaxys, GenBank 201.0, MacVector 13, and more Premium Mar 28, 2014 Downloads and Upgrades: Sequencher 5.2, Syapse, CytoSure Interpret 4.5.3, and more Premium Jan 3, 2014 In 2013, Acquisitions, Clinical and Dx Applications Defined Bioinformatics Market Premium Jul 12, 2013 Karo Bio Selects Elsevier's Reaxys to Support Medicinal Chemistry Projects Premium Feb 8, 2013 Downloads and Upgrades: PubmiR, Cytoscape 3.0, DNAnexus, and more. Premium Jan 11, 2013 Elsevier Buys Aureus Sciences to Tap Into Medicinal Chemistry Market Premium Aug 3, 2012 People in the News: Pinaki Dey; Sudipta Sadhu; Rajiv Ram; and Others Premium May 8, 2012 UK Presses Ahead with Open-Access Policy Feb 28, 2012 Support Pulled from Bill Killing Open-access Publishing Jan 20, 2012 Downloads & Upgrades: OpenHelix Tutorial Suites application; SBMLToolbox-4.1.0 Premium Dec 9, 2011 Elsevier Acquires Ariadne Genomics to Complement Existing Workflow Solutions Premium Dec 8, 2011 Elsevier Buys Ariadne Genomics Aug 5, 2011 Elsevier Strengthens Link between Databases and Journals with Launch of Genome Viewer Browser Premium Aug 3, 2011 Plasticell, Stemnion Team on Stem Cell Differentiation Protocols Aug 2, 2011 BioMarCare, Ariadne Use Grant to Develop Colorectal Cancer Dx Jul 29, 2011 Ariadne to Provide Pathway Analysis Instruction for Affy's Gene Expression Training Program Premium Jul 28, 2011 Ariadne Chosen as Partner in Affymetrix's Gene Expression Training Program Jul 1, 2011 Downloads and Upgrades Jul 1, 2011 Premium 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.