INTERIUM-PHOTOS

Secondary findings topic of discussion at ASHG panel discussion

HudsonAlpha’s Clinical Sequencing Exploratory Research project was the focus of several presentations at the American Society for Human Genetics annual meeting in Orlando, Fla. Secondary findings were the topic of a Thursday panel discussion. HudsonAlpha senior scientist Michelle Thompson, PhD, discussed secondary findings from the CSER project, in which children with developmental delay and other
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Genome Gateway™ communication software solution highlighted at ASHG

Web-based software eases onboarding, offers education for patients, research participants Orlando, Fla. – Genome Gateway™, a web-based software portal created by HudsonAlpha Institute for Biotechnology in Huntsville, Ala., was highlighted in a presentation at the American Society of Human Genetics (ASHG) annual meeting in Orlando. Genome Gateway™ manages interactions between genomic medicine patients and clinicians
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Genomic Medicine Newsletter: October 2017

Check out this month’s edition of the Genomic Medicine Newsletter and learn more about upcoming events, a newborn whole genome sequencing project and case studies at Smith Family Clinic. https://hudsonalpha.org/genomic-medicine-newsletter  
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Front Line Genomics features the Hero Fund

Front Line Genomics, the media sponsor for this year’s Genomic Medicine Conference, highlighted the HudsonAlpha Hero Fund in the October issue of its magazine. “We knew there were many, many patients, both pediatric and adult, who would benefit from a molecular diagnosis, and who had not had the opportunity to go through that diagnostic process,”
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Smith Family Clinic featured in Rare Revolution Magazine

Smith Family Clinic for Genomic Medicine and HudsonAlpha were recently featured in a special edition of Rare Revolution Magazine.   Rare Revolution is a UK-based digital magazine giving a voice to patients affected by rare conditions and the charities that represent and support them. The September edition focused on genomics, clinical trials and rare disease
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DNA sequencing vs. genotyping

Smarter Every Day, an educational video series created by Huntsville native Destin Sandlin, featured HudsonAlpha Institute for Biotechnology in its latest video about DNA sequencing. Educational Outreach Vice President Neil Lamb, PhD, explained the difference between DNA sequencing and genotyping. “With DNA sequencing, I’m reading through every single letter in your genome. With genotyping, I’m going
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Diagnostics leveraging next-generation sequencing become mainstream for rare disease diagnosis

Clinic Medical Director David Bick, MD, sat down with Clinical OMICs magazine to discuss the use of next-generation sequencing (NGS) for the identification and treatment of rare disease. “We are rapidly reaching the point where we do whole genome sequencing on anybody you think has a rare disease,” said Bick. Read the full story on page
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HudsonAlpha, UAB awarded $10M for newborn whole genome sequencing project

Huntsville, Ala. — HudsonAlpha Institute for Biotechnology, a nonprofit genomics and genetics research institute in Huntsville, Ala., in collaboration with the University of Alabama at Birmingham (UAB) School of Medicine and the University of Mississippi Medical Center, has been awarded a four-year, $10 million grant from the National Institutes of Health (NIH) to investigate how
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Genomic Medicine Newsletter: July 2017

Check out this month’s edition of the Genomic Medicine Newsletter and learn more about upcoming events, open recruitment for the Alabama Genomic Health Initiative and a Smith Family Clinic patient who received a diagnosis through the Hero Fund. Didn’t receive it? Subscribe today and have it delivered right to your inbox. http://hudsonalpha.org/genomic-medicine-newsletter.  
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HudsonAlpha ‘Hero Fund’ brings hope to patients in need

Huntsville, Ala. – HudsonAlpha Institute for Biotechnology is giving patients a chance at finding a diagnosis with the Hero Fund. Established by an anonymous donation to the HudsonAlpha Foundation, the Hero Fund helps patients at Smith Family Clinic for Genomic Medicine who need, but cannot afford, access to genomic medicine. Smith Family Clinic, powered by HudsonAlpha,
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