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GENETIC TOOLS UNCOVER CAUSE OF CHILDHOOD SEIZURE DISORDER MISSED BY OTHER METHODS

August 13, 2018

Aaron Quinlan and Gabor Marth from the USTAR Center for Genetic Discovery, use computational tools to find mutations responsible for early infantile epileptic encephalopathy.

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Running to Support the PENELOPE Undiagnosed Disease Clinic

April 23, 2018

Local events are a great way to get involved in genomics research. Participate in a local fun run to support Utah’s Penelope Undiagnosed Disease Clinic.

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Collaboration with Janssen Advances Critical Research

March 16, 2018

Deb Neklason, Marcus Pezzolesi and John Bohnsack from the University of Utah are collaborating with Janssen Research and Development LLC  to study colorectal cancer, diabetic…

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Finding the Story Within: Utah Genome Project at the 2018 Sundance Film Festival

January 31, 2018

Mark Yandell, PhD, Professor of Human Genetics and Co-Director of the USTAR Center for Genetic Discovery, along with University of Utah collaborators and fellow UGP…

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BBC News Feature: Handheld device sequences human genome

January 31, 2018

BBC News reports on the latest technological device used to sequence the human genome.

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GIGGLE: Scanning Genome Databases Faster to Accelerate Identification of Disease

January 29, 2018

Ryan Layer, Ph.D., senior postdoctoral fellow in Aaron Quinlan’s lab at the Department of Human Genetics at U of U Health and the USTAR Center for…

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Technology Milestone: Scientists Sequence Human Genome with Pocket-Sized Device

January 29, 2018

Aaron Quinlan, PhD, Associate Professor of Human Genetics and Co-Director of the USTAR Center for Genetic Discovery, and his graduate student, Tom Sasani, develop a…

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Largest Genetic Study of its Kind to Date Leads to Deeper Understanding of Heart Defects in Children

December 7, 2017

Dr. Mark Yandell and collaborators, Drs. Martin Tristani-Firouzi and H. Joseph Yost, take part in a large national “Bench-to-Bassinet” NIH consortium to study congenital heart…

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Leveraging Bioinformatics to Personalize Cancer Treatments

November 13, 2017

Yi Qiao, PhD, in the Department of Human Genetics and the USTAR Center for Genetic Discovery uses a computer algorithm to help clinicians treat cancer more effectively.

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American Heart Association Interviews University of Utah Researchers

November 3, 2017

Watch this American Heart Association video of U of U researchers discussing the importance of understanding the causes of congenital heart disease.

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University of Utah Health Collaborates with Janssen Research & Development to Investigate the Genetics of Suicide

November 3, 2017

Researchers at the U of U, in collaboration with Janssen Research and Development LLC, search genetic clues to better understand the relationship between suicidal behavior and psychiatric conditions.

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University of Utah Health Awarded $3 Million to Accelerate the Integration of Precision Medicine into Patient Care

October 2, 2017

Drs. Gabor Marth and Martin Tristani-Firouzi use a software tool, iobio, to assist doctors with providing clinical care based on information found within their patient’s DNA.

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New Tools to Mine Health Datasets May Uncover the Genetic Causes of Heart Defects

August 7, 2017

Mark Yandell, Ph.D., professor of human genetics and director of the USTAR Center for Genetic Discovery has created new tools, CAE and WARP, to uncover…

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mobile sequencing, genome sequencing, minion, nanopore, long-read sequencing, viral mutagenesis

Tiny tools for big data

July 13, 2017

The Quinlan Laboratory is using the diminutive MinION genome sequencing device to study viral genome evolution.

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congenital heart disease, data science, big data, heart, genetics, genomics, pediatrics, population health

Using data science to understand congenital heart disease

June 22, 2017

Dr. Yandell and Dr. Quinlan from the USTAR Center for Genetic Discovery were awarded a grant from the American Heart Association to use innovative data science technologies to uncover the genetic and environmental causes of congenital heart disease.

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