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Inside DNAnexus

Product updates, industry insights, opinions and references. From the team powering the Genomics Revolution.

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Cristin Smith

Cristin Smith

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About DNAnexus

DNAnexus provides a global network for sharing and management of genomic data and tools to accelerate genomic medicine. The DNAnexus cloud-based platform is optimized to address the challenges of security, scalability, and collaboration, for organizations that are pursuing genomic-based approaches to health, in the clinic and in the research lab.

The DNAnexus team is made up of experts in computational biology and cloud computing who work with organizations to tackle some of the most exciting opportunities in human health, making it easier—and in many cases feasible—to work with genomic data. With DNAnexus, organizations can stay a step ahead in leveraging genomics to achieve their goals. The future of human health is in genomics. DNAnexus brings it all together.

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Recent Posts

Deep Dive into DeepVariant
Discussing the State of Biomedical Data & Looking Towards the Future at PMWC
See our Talk at HiMSS 2019 – Integrating Clinico-Genomic Data for Precision Health
HiMSS 2019 – Enabling Rapid Advancement of Precision Health & Drug Discovery at Scale
Highly Accurate SNP and Indel Calling on PacBio CCS with DeepVariant
PAG 2019: Pioneering Frontiers in Genome Assembly
2018 Highlights: Expanding Beyond Secondary Analysis and Scaling up Collaboration
Implementing an RNA-Seq pipeline on DNAnexus
Battling Aligners: Benchmarking Tools on Mosaic with Mock Metagenomes
DNAnexus at ASHG: Elevating Translational Informatics

Top Posts

Deep Dive into DeepVariant
Comparison of BGISEQ 500 to Illumina NovaSeq Data
Evaluating DeepVariant: A New Deep Learning Variant Caller from the Google Brain Team
Training and Applying Genomic Deep Learning Models
Dot: An Interactive Dot Plot Viewer for Comparative Genomics
Evaluating the Performance of NGS Pipelines on Noisy WGS Data
Amplifying Google's DeepVariant
Highly Accurate SNP and Indel Calling on PacBio CCS with DeepVariant
Breaking Down Crumble: A New Method to Significantly Reduce NGS Data Footprint while Preserving Results
precisionFDA: Why It Matters

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