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Recent advances in long-read sequencing have allowed researchers to improve the accuracy of assemblies through longer contiguous sequences, allowing reads to span repeat elements and unambiguously ...

Recent advances in next-generation sequencing (NGS) technologies, increasing cost pressures, and regulatory uncertainties have driven pharmaceutical (pharma) and healthcare business models from ...

DNAnexus Supports Data Management & Genomic Analysis for a Global Research Consortium "The DNAnexus global network provides hundreds of researchers at institutions worldwide secure and immediate ...

De novo genome assembly is a complex task made more challenging by high levels of genetic diversity, repetitive elements, and duplicated genomic regions. Plant species are especially challenging ...

Learn how a leading global biologics research and development company embarked on an ambitious plan to accelerate the discovery of new therapeutic targets through population genetics on a cohort of ...

DNAnexus Apollo™ enables precision research by empowering bioinformaticians, data scientists, biologists, and clinician researchers to explore and analyze omics and clinical data together, on a ...

DNAnexus Titan™ is a flexible, cloud-based solution that brings multi-omics data and pipelines together in one place for streamlined analysis. DNAnexus Titan powers a standardizable, scalable, and ...

Ultragenyx, a biopharmaceutical company based in Novato, CA, is committed to bringing novel products to patients for the treatment of rare and ultra-rare diseases, with a focus on serious and ...

DNAnexus Titan powers the future of genomics research and clinical pipelines with trusted, high-performance cloud-based data analysis solutions. Let us do the heavy lifting for your NGS analysis ...

DNAnexus Apollo shatters big-data bottlenecks to release the power of genomics and multi-omics in translational research. View Case Study

Clinical diagnostics companies are rushing to unlock the power of genomics to deliver on the promise of precision medicine. However the volume of genomic data presents scalability, reliability, and ...

Genetic disorders are a leading cause of morbidity and mortality in infants. Rapid whole-genome sequencing (rWGS) can diagnose genetic disorders in time to change acute medical or surgical management ...

DNAnexus announced that Stanford University, the Data Coordination Center (DCC) for the National Institutes of Health (NIH)-funded ENCyclopedia of DNA Elements (ENCODE) Project, a flagship functional ...

Recent advances in long-read sequencing have allowed researchers to improve the accuracy of assemblies through longer contiguous sequences, allowing reads to span repeat elements and unambiguously ...

Recent advances in next-generation sequencing (NGS) technologies, increasing cost pressures, and regulatory uncertainties have driven pharmaceutical (pharma) and healthcare business models from ...

DNAnexus Supports Data Management & Genomic Analysis for a Global Research Consortium "The DNAnexus global network provides hundreds of researchers at institutions worldwide secure and immediate ...