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DNAnexus Apollo™
Multi-omics Data Science Exploration, Analysis & Discovery
DNAnexus Titan™
Next-Generation Sequencing Data Analysis
DNAnexus Portals™
Customized, Private & Collaborative Environments
DNAnexus GxP Support
Regulatory & Quality Services for Clinical, Manufacturing, & Laboratory Practices
UK Biobank Research Analysis Platform
An all-in-one platform: secure, compliant cloud infrastructure + tools + UK Biobank data
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Translational Informatics
Population Genomics
Genomic Analysis
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Molecular Pathology
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Inside DNAnexus
Product updates, industry insights, opinions and references.
From the team powering the Genomics Revolution.
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More Rapid Responses to Rare Disease
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How Regeneron Bypasses Bottlenecks to Iterate at the Scale and Speed of Science
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How DNAnexus Enables Human Longevity to Optimize Genomics Analysis and Interpretation for Healthy Individuals
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New Research Analysis Platform Enables UK Biobank To Exponentially Increase Size and Scale of World’s Most Comprehensive Biomedical Database
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The Hybrid Hackathons of the Future — now with Librarians!
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Better Together: Regeneron & HLI Share Their Experiences with DNAnexus & AWS
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Visit us at Bio-IT World 2021!
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Computational Immunology: Tailoring Tools to Tackle the T-Cell Triad
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How New Practices in Biomedical Research are Changing the Future of Healthcare
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How Multi-Omics is Changing Biomedical Research
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An Introduction to Population Genomics Studies with DNAnexus Apollo
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MIODx: A Breakthrough Leader in the precisionFDA COVID-19 Precision Immunology App-a-thon
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Responding to the Evolving World of COVID-19 Through Global Collaboration
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DNAnexus Platform and Product Updates: 2020 in Review
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Looking Beyond Causative Variants to Help Rare Disease Researchers Identify Elusive Treatment Options
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New UK Biobank Exome Pipeline: A 1-Button Read-Mapping Protocol for Public Sequencing Datasets
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2020 Vision: What Have We Learned?
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Deciphering the TCR Repertoire
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DipAsm: A Method for Generating More Accurate Phased Assemblies
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NEW: Monitor your Diagnostics Pipeline with the Case Management Portal
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MDA and DNAnexus Partner to Improve Neuromuscular Patient Care and Accelerate Drug Discovery
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From Pharmacogenomics to new Benchmarking Frameworks, DNAnexus Delivers at ASHG20
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How to Get Reliable Variant Calling in Repeat-Rich Regions
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Improving Therapeutic Development at Biogen with UK Biobank Data, Databricks, and DNAnexus
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Diving Deep into the Data Ocean
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DNAnexus R&D Report: Benchmarking Germline Variant Calling Pipelines
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UK Biobank Democratizes Data Access with its own Cloud-Based Data Analysis Platform
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How Myriad Genetics is Powering AI & Machine Learning Advancements in Precision Medicine
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Bold Innovation for a Promising Future
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Running RStudio Shiny Server and Apps on DNAnexus
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Embracing Open Standards to Build Portable, Reproducible Pipelines
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Three Ways to Leverage Translational Research for the Understanding of Complex Disease
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2022 Forecast: Responding to the Rising Tide of Diagnostic Tests
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Partnering with NVIDIA Clara Parabricks to Accelerate NGS Data Processing
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Being Productive during COVID-19 Quarantine
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A New Way to Play in May: Brush Up On Bioinformatics From Home
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Self-Servicing Archiving Now Available for DNAnexus on Azure
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Truth V2 Challenge on precisionFDA: Calling Variants in Difficult-to-Map Regions using short, long, and linked read sequencing
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Will COVID-19 Power a New Era of Precision Medicine?
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DNAnexus is going “virtual”! — Bio IT World 2020
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Trending topics in bioinformatics/AI: a deep learning approach to antibiotic discovery
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Bioinformaticians for Good: DNAnexus Aids in Open Science Collaborations In Fight Against Coronavirus
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Our Commitment to our Customers and Partners During Coronavirus (COVID-19)
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BWA-MEM2 Review: Should You Upgrade?
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Doubling Down on Next Generation Sequencing: How TwinStrand Biosciences and DNAnexus Work Together
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DNAnexus Platform Updates: A Year in Review
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DNAnexus Celebrates Rare Disease Day
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Hackathon-ing into DNAnexus
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Building a Precision Medicine Hub
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What Does the Sunsetting of Python 2.7 Mean for You?
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Refining GWAS Results Using Machine Learning
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A Tale of Two Cities: Breaking Down Data Barriers to Deliver Precision Medicine
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Designing Bioinformatics Pipelines for Fast Iteration
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Providing Bioinformatics Solutions to Address Challenges with Structural Variants
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Addressing the Complex Storage and Archival Needs of DNA Sequencing Data
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Scaling to Meet the Demands of Rare Disease Genetics
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Building a GenomeArk on the Cloud
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ASHG 2019: Delivering on the Promise of Precision Medicine
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DNAnexus Scoops European Innovations Award at SCOPE
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Why Medical Centers Should Prioritize HITRUST in Cloud Providers
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Considering an IT Investment For Your Clinical Diagnostics Lab? Help is Here
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Examining Variation from Wet-Lab Protocol Choices in Microbiome Data through the Mosaic Standards Challenge
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DNAnexus Detectives: Using Amazon Web Services to Help Solve a Medical Mystery
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DNAnexus Navigation and UI Changes
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By George! DNAnexus CTO George Asimenos Recognized as Top Voice in Precision Medicine
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Another Feather in the Cap for PrecisionFDA Platform: A 2019 FedHealthIT Innovation Award
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Teaming Up To Improve Outcomes for Multiple Sclerosis Patients
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From Manhattan Plot to BigTop: DNAnexus Makes Data Visualization a (Virtual) Reality
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Helping Scientists Discover the Hidden Jewels Within UK Biobank Data
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Bio-IT World 2019: Explore Millions of Variants in the UK Biobank Data
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Deep Dive into DeepVariant
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Discussing the State of Biomedical Data & Looking Towards the Future at PMWC
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Conferences
See our Talk at HiMSS 2019 – Integrating Clinico-Genomic Data for Precision Health
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HiMSS 2019 – Enabling Rapid Advancement of Precision Health & Drug Discovery at Scale
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Highly Accurate SNP and Indel Calling on PacBio CCS with DeepVariant
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PAG 2019: Pioneering Frontiers in Genome Assembly
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2018 Highlights: Expanding Beyond Secondary Analysis and Scaling up Collaboration
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Implementing an RNA-Seq pipeline on DNAnexus
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Battling Aligners: Benchmarking Tools on Mosaic with Mock Metagenomes
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Announcing the Results of Mosaic Clinical Strain Detection Challenge
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Parliament2: Fast Structural Variant Calling Using Optimized Combinations of Callers
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Investigating Differences Between Simulated and Real FASTQ DNA-Seq Data
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SMRT APAC Genome Assembly Grant & Upcoming Webinar
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Breaking Down Crumble: A New Method to Significantly Reduce NGS Data Footprint while Preserving Results
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Comparison of BGISEQ 500 to Illumina NovaSeq Data
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Announcing the Winners of Mosaic Microbiome Community Challenge: Strains #1
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PrecisionFDA Receives FDA Commissioner’s Award for Outstanding Achievement
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SMRT Leiden Assembly Grant
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Training and Applying Genomic Deep Learning Models
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DNAnexus expands with Microsoft Azure Cloud Platform
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Bio-IT World 2018: Transforming Biological Insights to Accelerate Translational Research
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Shaping the Future of Precision Medicine for Newborns
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One Genome Browser to Rule Them All?
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Amplifying Google’s DeepVariant
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We’re coming to the Windy City for AACR
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The Case for Rapid Genome Sequencing – Saving Critically Ill Newborns
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GDPR Compliance – What you need to know
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Regeneron Genetics Center Identifies Promising Target for Development of New Therapies for Chronic Liver Disease
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How to Train Your DRAGEN – Evaluating and Improving Edico Genome’s Rapid WGS Tools
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Integrating Multiple Data Sources to Power Discovery and Analysis
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Conferences
Advancing Microbiome Research through Community Engagement
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Mosaic Microbiome
Benchmark and Advance Computational Methods for Targeted Strain Detection
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Tri-Con 2018: Leveraging the Cloud to Power Multi-Omics Research
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Countdown to AGBT 2018
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Conferences
Analysis Commons: A Collaborative Approach to Multi-Omics Discovery
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PMWC 2018: Leveraging Multi-Omic Datasets in Discovery & Clinical Trials
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Evaluating the Performance of NGS Pipelines on Noisy WGS Data
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Dot: An Interactive Dot Plot Viewer for Comparative Genomics
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Announcement
PAG 2018: A Focus on Genome Assembly
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CIO Webinar Series: Genomic Data Privacy in the Cloud
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Industry News
Evaluating DeepVariant: A New Deep Learning Variant Caller from the Google Brain Team
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Announcement
Introducing htsget, a new GA4GH protocol for genomic data delivery
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Announcement
DNAnexus at ASHG: Accelerating Your Path from Genomic Data to Insight
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The New UI: Sleeker. Modern. Intuitive.
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Announcement
At Bio-IT World: Promoting Technological Innovation to Advance Precision Medicine
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Announcement
DNAnexus Celebrates National DNA Day
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Webinar: Trio Analysis with Sentieon Rapid DNAseq on DNAnexus
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Upgrading to TLS 1.2
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Case Study: Calling Somatic Variants with Sentieon on DNAnexus
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ACMG: A Look at Applying Genomic Data to Clinical Reports
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Conferences
Updated DNAnexus Impact Assessment for Cloudbleed: No evidence of exploitation.
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Case Study: Trio Analysis with Sentieon Rapid DNAseq on DNAnexus
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DNAnexus Not Impacted by Cloudflare Information Leak (“Cloudbleed”)
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Innovation Fueled by Collaboration and Regulatory Science
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New Org Admin Tools Available on DNAnexus
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Sentieon on DNAnexus: License-Free Access Through April 7th
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Announcement
Salute! Nexus Negronis On Us at AGBT!
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Bringing Together Genomics and Patient Data in the Cloud
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Collaborative Genomics: Highlights From 2016
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DNAnexus & TCGA: Reanalyzing the World’s Largest Pan-Cancer Initiative Dataset
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Ten-Fold PacBio Sequel Call Set Proves Affordable & Effective in Identifying Structural Variants
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Join Us for a Lunchtime Discussion at ASHG
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DNAnexus Heads to Festival of Genomics
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Cloud Bioinformatics Made Easy: A Workshop with SCGPM
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The U.S. Cancer Moonshot and a Culture of Collaboration
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Countdown to Beantown: DNAnexus at Festival of Genomics
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#GenomeFest
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Once in a Blue Moon Competition: precisionFDA Truth Challenge
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Frost & Sullivan Recognizes DNAnexus as the Enabling Technology Leader in the Global Genomics Industry
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Industry News
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Announcement
Webinar Series: Enabling PacBio Long-Read Bioinformatics in the Cloud
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At Bio-IT World: Technological Innovation Advancing Genomic Science and Medicine
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#BioIT16
Precision Medicine from Birth
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One Global Cloud Platform Unites Researchers to Shed Light on Autism
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Just Published New England Journal of Medicine Paper From Geisinger and Regeneron Highlights Value Of Integrating Genetic and EHR Data on DNAnexus
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Cloud-based Genomics at the White House
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#PrecisionMedicine
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The Future of Precision Medicine
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Supporting Innovative Open Access Cancer Genomics Pilot
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DNAnexus Made Ridiculously Simple
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DNAnexus Heads to Orlando for AGBT 2016
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Advances in Genome Biology and Technology
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AGBT
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AGBT16
DNAnexus in Real Life: Tackling Precision Medicine Through Real-Time, Multi-Institution Cancer Collaboration
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A Look Back at 2015
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DNAnexus Presents at JP Morgan Healthcare Conference
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#JPM16
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Business
precisionFDA: Why It Matters
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Supporting Freebayes, to Serve Our Customers and the Community
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Cancer Genomes Dataset Now Hosted on Amazon Web Services
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Highlights from Festival of Genomics California 2016
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#GenomicsFest
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Conferences
Festival of Genomics: Not Your Typical Genomics Conference
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Post-ASHG: The Future of Genomics & Informatics in the Next 5 Years
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#ASHG15
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American Society of Human Genetics
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Conferences
Precision Medicine: Seeking Impact, Needing Champions
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Conferences
New 3000 Rice Genomes AWS Public Dataset – Easy Access on DNAnexus Platform
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Announcement
Using Genomics To Improve Patient Care: DNAnexus to Support Both Projects Selected by California Precision Medicine Initiative
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Industry News
Natera’s Genetic Testing to Scale with DNAnexus
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Help Save the Black Rhino
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DNAnexus Honored in MIT Technology Review’s 50 Smartest Companies of 2015
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Precision Medicine Improves Survival without Increasing Costs
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Big Data Rice Research Helps to Feed the World
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Announcement
The Word “Genetics” is 110 Years Old
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Obama’s Precision Medicine Initiative: DNAnexus is There
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Industry News
On A Day When Apple Sidesteps Healthcare Technology, Mary-Claire King Shows How To Confront It
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Industry News
DNA Day: Celebrating the Decades-long Unraveling of DNA
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AGBT Posters Featuring DNAnexus
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Feb 28: Celebrating Rare Disease Day
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2014: The Year of the Cloud
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Cloud Computing
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One Simple Solution for Ten Simple Rules
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On DNA Day, We’re Thinking About (What Else?) Data
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Dispelling the Myths of the Cloud
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Amazon cloud
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Happy Holidays to All!
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Sequence Data: The View from JP Morgan
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Conferences
Streaming an entire sequencing center across the Internet
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Next-gen sequencing and the cloud – revolutionary, or hype?
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