Welcome to the repository for all things DNAnexus. Sort through case studies, webinars, white papers, and videos by their associated DNAnexus product and key topics for a deeper dive into the power of our platform and expertise.
Cost Savings And Business Benefits
Enabled By The DNAnexus Platform
A FORRESTER TOTAL ECONOMIC IMPACT STUDY
DNAnexus, a cloud-based precision health data management and analysis platform, offers several advantages over DIY solutions.
How clinical diagnostic labs can flexibly scale to meet the demand for increased NGS test volume.
Learn how Eli Lilly partnered with DNAnexus and used open-source standards to tackle the changing bioinformatics landscape with on-demand compute and portable, reproducible pipelines to run in any region.
Your team members contribute the most when they’re focused on science, not when they’re spending valuable time fixing and optimizing your bioinformatics system.
Large-scale omics datasets are revolutionizing how pharmaceutical companies identify targets for therapeutic development, and have become one of the main paths in accelerating precision medicine.
Advancing Rare Disease Therapeutics with DNAnexus Titan™
Ultragenyx chose to implement DNAnexus Titan™, a unified NGS analysis platform, to bring data and pipelines together in one secure environment for streamlined multi-omics data analysis.
A bioinformatics solution is the backbone of any successful precision medicine initiative.
Discover the Difference
De novo genome assembly is a complex task made more challenging by high levels of genetic diversity, repetitive elements, and duplicated genomic regions.
Do you have the right informatics strategy to get to insights quickly while working with the UK Biobank (UKB) dataset?
rWGS is a unique, high-cost healthcare innovation that appears to improve healthcare outcomes while decreasing cost of care.
Learn how Human Longevity inc. used the DNAnexus Titan Platform on Amazon Web Services to streamline their genomics infrastructure. This enabled the company to focus on product improvements over maintenance of infrastructure.
With a single CGP test, we can interrogate hundreds of genes, using less tissue and increasing the probability of detecting actionable findings.
RStudio Workbench Trial Version is now available on the UK Biobank Research Analysis Platform, allowing users to use RStudio in their analysis. This session covers everything you’ll need to know to start working with the application and use...
Coming from high performance computing? Learn equivalent cloud-based methods for running bioinformatics jobs quickly on the Research Analysis Platform.
Learn from thought leaders from Regeneron and DNAnexus.
Watch the panel of expert cardiovascular disease researchers as they discuss the latest advances in their field of study. They discuss their research experience, recent advances and potential roadblocks
Learn how to create notebooks, dashboards and incorporate Shiny apps all in the cloud on the Research Analysis Platform.
A panel of research experts discuss the landscape of Dementia research, including the Demon Network hackathon, incorporating large-scale datasets, and the importance of cloud computing and global scientific collaboration networks.
Learn about the data formats available to start running your image analysis on the Research Analysis Platform. Ondrej Klempir, Sr. Community Engagement Scientist at DNAnexus, walks you through how to access the data, reviews basic image...
This introductory session covers basic Cloud Computing concepts that will set you up for success on the Research Analysis Platform. Topics discuss include basic cloud computing concepts, selecting instance types, and the basics of running apps on files in your...
This session details visualizing GWAS results using the Research Analysis Platform. The webinar covers interactive exploration of GWAS results using the LocusZoom App and then dives deeper into variant annotation and visualization using both R and...
Experts from Regeneron, NVIDIA, UK Biobank & DNAnexus review the exact analysis pipeline used to quickly generate the 450,000 reference data set.
DNAnexus Experts elaborate on the starter example from our introduction to WDL webinar and add more complexity to our WDL script. Then they introduce more syntax and discuss how to use WDL with the Docker environment.
DNAnexus experts take you through creating a starter WDL script and explain the basics of WDL syntax and how to use it on UKB RAP. They then compare it with native DNAnexus workflows and provide you tips on how to decide when to use WDL.
DNAnexus experts give you an introduction to the applet and workflow development process by building a simple project that works on Bulk files on RAP.
An introduction to running GWAS using Regenie on the Research Analysis Platform. DNAnexus experts demonstrate how to run the analysis using a diabetes phenotype on the 300k data.
Learn about the mission of the UK Biobank, the new 300k whole exome sequencing data release and how to become an approved researcher from experts at UK Biobank, Regeneron, and DNAnexus
Ever wonder which bioinformatics workflow description and management systems you should be using? We assembled a roundtable of experts from bioinformatics workflow frameworks including CWL, WDL, and Nextflow.
An introduction to using the Research Analysis Platform to explore and analyze the uniquely rich UK Biobank dataset
Learn how to run apps, applets, and workflows on the UK Biobank Research Analysis Platform.
Go in-depth analyzing the uniquely rich UK Biobank dataset with Jupyter notebooks. Learn how to utilize Jupyter Notebooks and Apache Spark to explore and analyze UK Biobank’s trove of phenotypic and health record data, covering 500,000 volunteer...
An introduction to using Jupyter Notebooks on the Research Analysis Platform, to explore and analyze the uniquely rich UK Biobank dataset.
Hear from experts from popular variant annotation platforms, OpenCRAVAT and BioProdict, and learn pros and cons of each software platform for certain projects.
Ankita Das, Head of Product at MIODx, discusses methods for analyzing and interpreting TCR data in the context of biomarker discovery for inflammatory diseases.
Ben Busby showcases best practices for integrating epigenetic data with phenotypic data at scale to conduct powerful research studies.
Learn about leading technologies and real world examples of how machine learning is used in biomedical research including how to accelerate single cell genomic analysis using NVIDIA RAPIDS, and achieve 100x faster clustering and visualization.
DNAnexus Principal Scientist John Didion walks through how to run WDL workflows both locally and on DNAnexus.
DNAnexus Principal Scientist John Didion walks through how to use public Docker containers as part of an application and highlights best platform practices.
How Regeneron Genetics Center (RGC) collaborates with 30 institutions to build one of the world’s most comprehensive genetics databases, pairing sequenced exomes with de-identified records of more than 120,000 people to date
Overview of the growing St. Jude Cloud datasharing platform that includes more than 5,000 whole-genome, 5,000 whole-exome and 1,200 RNA-Seq datasets from more than 5,000 pediatric cancer patients and survivors.
The VGP aims to create reference quality genome assemblies of all vertebrate species on earth. Presented in this webinar is Phase I of the project.
Today’s genomics landscape is rapidly evolving with the accelerated adoption of multi-omics by biopharma organizations, clinical diagnostics companies, and healthcare systems.
Dedicated to Detecting Ultra-Rare Variants with Unparalleled Sensitivity and Specificity
TwinStrand chose DNAnexus to provide the scalable and secure cloud infrastructure it needed to support customers of its DuplexSeq™ kits.
NGS data analysis management systems are the backbone of your dry lab, providing vital functionality for day-to-day workings of your business delivery.
While modern-day drug discovery lacks the drama of Greek mythology, we are still faced with the odyssey of how to deliver on the promise of genomics-based precision medicine.
The promise of precision medicine and better patient outcomes is here, through the utilization and application of genomic data in biomarker discovery and clinical research.
Learn why the FDA, top pharmaceutical companies, global diagnostic test providers, genome centers and sequencing service providers have trusted DNAnexus to support their global genomics programs.
Discover the Difference
Learn about our experience with Microsoft Azure in this ebook. The Microsoft Cloud empowers organizations to re-envision the way they bring together people, data, and processes that better engage patients and optimize clinical and operational effectiveness.
You’ve jumped ahead of the curve, leveraging next-generation sequencing (NGS) to advance precision medicine for better patient care, and you are now experiencing an explosion of demand.
DNAnexus Platform enables researchers and clinicians to focus on their genomic analyses while complying with regulations, laws and industry expectations for security and privacy.
Learn how one company chose to use DNAnexus Apollo for analysis and visualization, which provided a scalable cloud environment.
The underlying infrastructure that DNAnexus provides, allows us to focus on our core competencies of R&D and patient care.
The goal of the ENCODE Project is to comprehensively catalog candidate functional and regulatory elements of the human genome, and provide a foundation for studying the genomic basis of human biology and disease.