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Angela Anderson

 

 

 

Did you know that a loss of function mutation in the MEPE gene, which codes for proteins that regulate bone mineralization, results in two-fold increased odds of osteoporosis and 1.5-fold increased risk of fractures?ZJSwimsuit The enigmatic sea bikini with a high waist, bikini bikini, bikini for vacation Neither did scientists, until they delved deeply into data released by the UK Biobank.

The UK Biobank, which has developed a biospecimen collection paired with unparalleled health data and phenotype information from more than 500,000 individuals, is making its massive genotype/phenotype dataset available to approved researchers world-wide, as part of a unique open access project aimed to accelerate medical research and drug discovery. Earlier this month, it released the first batch of results of whole-exome sequencing, providing data from 50,000 people. These exomes were sequenced by the Regeneron Genetics Center, which will soon complete sequencing of the entire 500,000 person cohort with the financial support of a “pre-competitive” consortium of leading biopharma companies.

Contained inside these data is a treasure trove of information — but one in which the jewels are hidden among billions of grains of sand.Women's Long Sleeve Swimwear,Sun Predection Rash Guard Wetsuit Two Piece Swimsuit Set for Diving Beach Seaside

How would Dana, a senior scientific researcher in the early development cardiovascular program at a pharma company, use it to determine whether there is a correlation between mutations in the PKP2 gene and a phenotype trait, such as red hair?

Luckily, the new DNAnexus Cohort Browser for UK Biobank makes phenome-wide association studies (PheWAS) and other queries easy to carry out. Developed to help researchers like Dana navigate thousands of phenotypic fields and millions of genetic variants, the browser can mine extremely large datasets in a matter of seconds.

How does it work? Dana would simply plug in her phenotypic (red hair) and genetic (PKP2, familial links) requirements into a built-in browser with a powerful point-and-click interface that makes it easy for her to quickly filter, browse, and visualize the integrated phenotypic and genomic information.

Run on our DNAnexus Apollo Platform, the FLCH+YIGE Mens's 2 Piece Outfits Active Tracksuit Sweatsuits + Pants Set Sportswear was designed to enable scientists with all levels of bioinformatic expertise to be able to rapidly test multiple hypotheses and gain insight into mechanisms of action, biomarkers, and targets. And working with clinical data requires specialized capabilities to maintain privacy, which includes compliance in accordance with ISO 27001 certification, GDPR, and GxP, among others.

As part of their effort to explore the UK Biobank data, the Regeneron Genetics Center (RGC) used DNAnexus to run bioinformatics pipelines and deliver the results back to pharmaceutical companies in the UK Biobank Exome Sequencing Consortium. As part of this data delivery, the RGC successfully deployed the cohort browser on a collection of thousands of phenotypic fields extracted from the UK Biobank and millions of genetic variants computed through their scientific pipeline.

Initial analysis of the UK Biobank data has already led to many discoveries.

In addition to the MEPE mutation finding, RGC researchers identified a handful of other significant novel loss-of-function associations,ROBAG Outdoor Rock Climbing Rope, 8mm (16KN) 10.5mm (25KN) 12mm (32KN) High Strength Static Rappelling Safety Rope 2 Pieces Carabiners including one that confers a nearly five-fold increased odds of varicose veins in certain carriers.

Among the nearly four million single nucleotide and indel coding variants observed by the researchers were many mutations to the so-called “ACMG59” genes — 59 genes proposed by The American College of Medical Genetics to be associated with highly penetrant disease phenotypes.

Overall, 2% of the sequenced individuals carried a flagged variant in one of the ACMG59 genes. Variants in cancer-associated genes were the most prevalent, followed by variants associated with familial hypercholesterolemia and cardiac dysfunction disorders.

Importantly, the Browser for UK Biobank allows researchers to check their hypotheses against real-world data from the de-identified patients’ records. For instance, an individual with a pathogenic missense variant could be found to have a history of benign colon neoplasms, diverticular disease of the intestine, colonic polyps, and intestinal obstruction.

These discoveries are a great illustration of how the extensive health data available for UK Biobank participants will be a valuable resource to assess disease risk at both the individual and the population level.

The crowdsourcing spirit of the initiative is what makes it stand apart. When the Manchester-based biobank enrolled its first volunteer 13 years ago, principal investigator Rory Collins wanted to democratize the data and maximize its scientific pay-off: “By making data available to 100 people around the world, we can get a lot more research done than if I sit here and do one study a year with the data,” the University of Oxford epidemiologist told Science.

Earlier releases of genotyping data in 2015 and 2017 have already resulted in more than 600 papers across 1,400 projects from 7,000 researchers. Eoinch Limp Bizkit Mens Long Sleeve Sweatshirts Men's Hoodies BlackAdditional tranches of exome and whole genome data will similarly be released over the next two years.

The hope is that the easy-to-use DNAnexus Apollo Platform and its Cohort Browser for UK Biobank will help even more researchers navigate the complexities of generating and delivering the combined phenotype and genetic data.

“This is just the beginning,” said Aris Baras, MD, Senior Vice President and Head of the Regeneron Genetics Center. “There is so much actionable information in this resource that can be utilized by scientific minds around the globe. We are hard at work mining the data for novel findings that will accelerate science, innovative new medicines and improved patient care, and are excited to have others join us in this important quest.”

Researchers interested in applying for access to UK Biobank data should visit Rh Studio Ingreened Umbrella Pier Bay Sunset Large Double Layer Outdoor Rain Sun Car Reversible Umbrella.

For more information about the UK Biobank Cohort Browser, visitHUYANNABAO Daily Women Backpack for School Teenager Girls Nylon Travel Backpacks Female Casual Shoulder Bags.

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We are heading back to our second home in Boston to attend the annual Bio-IT World conference! Our team is excited to join fellow researchers, clinicians, pharmaceutical and IT professionals to discuss the future of precision medicine. Bsi Products Collegiate Virginia Big Spatula W Bottle OpenerThis year we are bringing our enhanced Doanpa Men PlusSize Jogger Active Workout Training Hood Tracksuit Set, which features a new, innovative clinico-genomic cohort browser that enables users to explore and analyze millions of genomic and clinical data points in a matter of seconds.

4 Liufeilong Hats, Camouflage Hats Spring Summer Influx Men's Baseball Caps Outdoor Caps Sun Hats Visors Breathable Net Caps YouthWe are excited to see that our trusted partner on this project, theProbrico 1 Pair Keyboard Drawer Sliding DSMH10220 Steel White Length 500mm 20 Furniture Cabinet Kitchen Cupboard Drawer Slides , has been recognized as a 2019 finalist for the Inaugural Innovative Practices Awards. Regeneron’s work performing exome sequencing and analysis for all 500,000 samples for the UK Biobank is a true achievement. We were honored to partner with them to create an innovative cohort browser for UK Biobank data, allowing researchers the ability to browse through 3,000 phenotypic fields and 15,000,000 genomic variants across 100,000 samples and build cohorts.

Stop by the DNAnexus booth #310 to learn more about the brand new Apollo for UKB! Check out our conference activities below. Can’t make it to any of our events? Request a meeting.

DNAnexus Booth Activities

DNAnexus ApolloDemo: Explore Millions of Genomic & Clinical Data Points with DNAnexus Apollo for UK Biobank

  • Wednesday, April 17: 10:00am-11:00am, 1:00pm-2:00pm
  • Thursday, April 18: 10:00am-11:00am

Mining large-scale datasets for actionable insights is a huge computational effort. The UK Biobank’s first release of their dataset presents an exciting new opportunity for genomics research, with 50,000 exomes and combined phenotypes for users to dig into.

DNAnexus Apollo is based on a scalable cloud-based platform. FANTAZIO Lazy Sloth Sports Duffle Bag Gym Bag Travel Duffel with Adjustable StrapWhether you’re working with the UK Biobank or your own protected data, DNAnexus Apollo streamlines consumption of multi-omics and clinical records from complex datasets.

Customer Talk/Poster

AI Assisted Rapid Clinical Whole Genome Sequencing for Critical Care
Bioinformatics Track

  • April 18, 2:30pm-3:00pm
  • Ray Veeraraghavan, PhD, Director of IT & Informatics, Rady Children’s Institute for Genomic Medicine

DNAnexus Apollo Lounge: Cocktail Networking Event

Join us during Bio-IT World for a special Greek-style networking event!JKYJYJ Design Adjustable Baseball Cap Unisex Pure color Sport Hat Women Snapback Cap for Men Cartoon Hip Hop Cap Bone

Eat, drink, and have fun meeting fellow scientists and other translational research industry experts.

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