This question is one we aspire to answer at Tute Genomics. Thus, it’s with tremendous excitement we announce today a new informatics project we have been selected to lead with Newborn Screening Ontario (NSO), one of the largest and most comprehensive newborn screening programs in the world, along with our partners at UNIConnect. Every year … Continue reading How many lives could be saved and significantly improved if genomic medicine began at birth for every child?
Category: Blog
Newborn Screening Ontario Inks Deal with Tute Genomics, UNIConnect Team to Deliver Informatics Infrastructure for NGS Testing
Deal between Tute, UNIConnect and Canada’s highest volume molecular testing lab will expand access to genomic medicine as province advances repatriation of genetic testing OTTAWA, Ontario, PROVO and SANDY, Utah, March 22, 2016 – Newborn Screening Ontario (NSO), which operates the highest sample volume laboratory in Canada for molecular testing, and Tute Genomics and UNIConnect … Continue reading Newborn Screening Ontario Inks Deal with Tute Genomics, UNIConnect Team to Deliver Informatics Infrastructure for NGS Testing
Tute Arrives at ACMG
Tute Genomics is visiting Tampa, FL this week to participate in the ACMG (The American College for Genetics and Genomics) Annual Clinical Genetics Meeting. This conference is a great opportunity to share our mission with others in our space–personalized healthcare is on the rise, and Tute is paving the way with our end-to-end infrastructure for … Continue reading Tute Arrives at ACMG
Variant Triage Based on Patient Phenotype is Key to Scaled NGS Testing
Webinar Info Date: Thursday, January 28th Time: 12:00pm ET Presenter: Bryce Daines, VP of Product, Tute Genomics Download Slides If your informatics infrastructure does not support phenotypic-driven variant triage, then it’s likely your NGS turnaround times are too long and your costs far too high. The problem is that today’s larger NGS tests produce too … Continue reading Variant Triage Based on Patient Phenotype is Key to Scaled NGS Testing
Tute Genomics Delivers Big in the Year of Genome-Guided, Precision Medicine
2015 was a milestone year for genomic medicine. Spurred by new CPT reimbursement codes in the US and massive government sponsored sequencing initiatives across the globe such as President Obama’s Precision Medicine Initiative, the multi-billion dollar genome-guided, precision medicine industry took a giant leap forward this past year. Here at Tute Genomics we are thrilled … Continue reading Tute Genomics Delivers Big in the Year of Genome-Guided, Precision Medicine
Tute is Keeping Austin Awesome at AMP
This week, Tute Genomics travels to Austin, TX to participate in the annual Association for Molecular Pathology (AMP) meeting. The theme of AMP this year is, “Realizing the Dream of Precision Medicine. Genomics is changing healthcare as we know it, and Tute is shaping the future of medicine: unlocking the genome, personalizing treatment, and powering discovery. Stop … Continue reading Tute is Keeping Austin Awesome at AMP
Tute Genomics Acquires Knome
Procurement of highly acclaimed genome interpretation technology from Knome fortifies Tute Genomics’ mission to catalyze precision, genome-guided medicine. PROVO, Utah, November 2, 2015 – Tute Genomics, the leader in clinical sequencing informatics, today announced the acquisition of key assets of Knome, a renowned human-genome interpretation company whose systems and services helped spearhead several of the … Continue reading Tute Genomics Acquires Knome
Tutorial: Diagnosing Inherited Hemolytic Anemia
Every person on the planet has somewhere between 3 to 4 million variants in their genome. These variants are responsible for the large range of diversity that we see in human beings. Some variants have very little impact on the way that an individual lives her life, while other variants can cause serious disease conditions. … Continue reading Tutorial: Diagnosing Inherited Hemolytic Anemia
Tute Arrives at NSGC
Today begins the 34th Annual Education National Society of Genetic Counselors (NSGC) Conference in Pittsburgh, PA where genetic counselors, scientists, and companies convene to better learn from one another regarding new developments in genetic counseling, medical genetics, and new technologies, theories, and practices that strengthens and support attendees’ practices. If you’re at NSGC this week, … Continue reading Tute Arrives at NSGC
Tutorial: Diagnosing Rare Genetic Disease
There are over 200 million rare diseases that affect people worldwide and it is estimated that over 80 percent of rare diseases have a genetic origin. Although each disease is rare, when you add all of the rare diseases together, they are actually surprisingly common. Some estimate that 1 in 10 people will be affected … Continue reading Tutorial: Diagnosing Rare Genetic Disease