Events Calendar

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A Behavioral Health Collision At The EHR Intersection
2014-09-30    
2:00 pm - 3:30 pm
Date/Time Date(s) - 09/30/2014 2:00 pm Hear Why Many Organizations Are Changing EHRs In Order To Remain Competitive In The New Value-Based Health Care Environment [...]
Meaningful Use and The Rise of the Portals
2014-10-02    
12:00 pm - 12:45 pm
Meaningful Use and The Rise of the Portals: Best Practices in Patient Engagement Thu, Oct 2, 2014 10:30 PM - 11:15 PM IST Join Meaningful [...]
Adva Med 2014 The MedTech Conference
2014-10-06    
All Day
Adva Med 2014 The MedTech Conference October 6-8, 2014 McCormick Place Chicago, IL For more information, visit, advamed2014.com For Registration details, click here  
Public Health Measures Meaningful Use
2014-10-09    
12:00 pm - 12:45 pm
Public Health Measures Meaningful Use: Reporting on Public Health Measures Join Meaningful Use expert Jim Tate for a three part series of webinars addressing MU [...]
2014 Hospital & Healthcare I.T. Conference
2014-10-13    
All Day
Join us at our 2014 Hospital & Healthcare I.T. Conference and experience the following: Up to 125 Hospital & Healthcare I.T. executives from America’s most prestigious [...]
Connected Health Care 2014
Key Trends That will be Discussed at the Conference! Connected Healthcare 2014 is set to explore the crucial topics that are revolutionizing the connected health industry: [...]
HealthTech Conference
2014-10-14    
All Day
HealthTech Capital is a group of private investors dedicated to funding and mentoring new "HealthTech" start ups at the intersection of healthcare with the computer [...]
Health Informatics & Technology Conference (HITC-2014)
2014-10-20    
All Day
Information technology has ability to improve the quality, productivity and safety of health care mangement. However, relatively very few health care providers have adopted IT. [...]
HIMSS Amsterdam 2014
2014-10-20    
12:00 am
About HIMSS Amsterdam 2014 This year, the second annual HIMSS Amsterdam event will be taking place on 6-7 November 2014 at the Hotel Okura. The [...]
Patient Portal Functionality and EMR Integration Demonstration
2014-10-22    
2:00 pm - 3:30 pm
This purpose of this webcast is to present a demonstration to show how the Patient Portal integrates with EMR, as well as discuss how this [...]
Connected Health Symposium 2014
Symposium 2014 - Connected Health in Practice: Engaging Patients and Providers Outside of Traditional Care Settings Collaborating with industry visionaries, clinical experts, patient advocates and [...]
CHIME College of Healthcare Information Management Executives
2014-10-28 - 2014-10-31    
All Day
The Premier Event for Healthcare CIOs Hotel Accomodations JW Marriott San Antonio Hill Country 23808 Resort Parkway San Antonio, Texas 78761 Telephone: 210-276-2500 Guest Fax: [...]
The Myth of the Paperless EMR
2014-10-29    
2:00 pm - 3:00 pm
Is Paper Eluding Your Current Technologies; The Myth of the Paperless EMR Please join Intellect Resources as we present Is Paper Eluding Your Current Technologies; The Myth [...]
Events on 2014-09-30
Events on 2014-10-02
Events on 2014-10-06
Events on 2014-10-09
Events on 2014-10-13
Events on 2014-10-14
Connected Health Care 2014
14 Oct 14
San Diego
HealthTech Conference
14 Oct 14
San Mateo
Events on 2014-10-20
HIMSS Amsterdam 2014
20 Oct 14
Amsterdam
Events on 2014-10-23
Events on 2014-10-28
Events on 2014-10-29
Press Releases

Texas Children’s researchers develop groundbreaking tool to boost genetic testing accuracy.

EMR Industry

HOUSTON (Oct. 6, 2025) – Researchers at Texas Children’s Hospital’s Duncan Neurological Research Institute (NRI) and Baylor College of Medicine have developed an advanced tool within the Genome Aggregation Database (gnomAD) to significantly improve the accuracy of genetic testing—offering major benefits for patient diagnosis and care worldwide.

Published in Nature Communications, the study introduces a method called local ancestry inference (LAI), which breaks down the genome into ancestry-specific segments, allowing for more precise interpretation of genetic differences.

“This research helps ensure our genomic databases better represent the full range of human genetic diversity,” said Dr. Elizabeth Atkinson, senior author, NRI principal investigator, and assistant professor at Baylor College of Medicine. “By refining allele frequency estimates in mixed-ancestry populations, we can make genetic diagnoses more accurate and reduce the chance of errors—helping patients from all backgrounds.”

The study, titled Improved Allele Frequencies in gnomAD through Local Ancestry Inference, marks a major advancement in genetic testing and personalized medicine. Co-first authors include Pragati Kore and Michael Wilson.

While genetic testing is crucial for diagnosing diseases, current tools often rely on population-wide averages that can overlook key ancestry-specific variations—especially in individuals with diverse backgrounds such as African/African American or Latino/Admixed American. This new approach helps uncover those hidden differences, leading to better and more equitable healthcare.

Dr. Atkinson’s team used local ancestry inference (LAI) to tackle the limitations of current genetic testing. Instead of analyzing the genome as a whole, LAI breaks it into segments based on different ancestral origins—such as African, European, or Indigenous American. The team then calculated how frequently each genetic variant appears within these ancestry-specific segments.

This revealed that many variants previously considered rare in global datasets are actually common within certain ancestral groups.

“These differences aren’t just academic,” said Dr. Atkinson. “They have real clinical impact.”

In populations labeled as African/African American and Latino/Admixed American, researchers found that over 80% of genetic sites had a higher frequency in at least one ancestry-specific segment than previously recognized. In some cases, these frequency shifts crossed a key threshold used by the American College of Medical Genetics and Genomics (ACMG) to classify a variant as benign—potentially leading to more accurate variant interpretations and reduced misdiagnoses.

The updated, ancestry-specific allele frequency data is now freely available through gnomAD, giving researchers, clinicians, and genetic testing labs around the world access to a more precise tool for interpreting genetic variation.

“Ancestry is complex, and using a single label for a patient doesn’t capture that complexity,” said Dr. Atkinson. “This research moves us closer to a more detailed and accurate understanding of genetic ancestry in clinical care.”

About Texas Children’s:
Texas Children’s is a nonprofit health care organization dedicated to improving the health of children and women around the world through excellence in patient care, education, and research. Consistently ranked as the top children’s hospital in Texas and among the best in the nation, Texas Children’s is widely recognized for its expertise and groundbreaking work in pediatric and women’s health.

The system includes several renowned facilities, such as the Duncan Neurological Research Institute (NRI), the Feigin Tower for pediatric research, and the Pavilion for Women—a leading OB/GYN center specializing in high-risk pregnancies. It also operates multiple hospitals, including Texas Children’s Hospital West Campus in West Houston, The Woodlands campus serving communities north of Houston, and the newly opened Texas Children’s Hospital North Austin, offering advanced pediatric and maternal care to Central Texas families.

Texas Children’s also established the nation’s first HMO for children, Texas Children’s Health Plan; operates Texas Children’s Pediatrics, the largest pediatric primary care network in the U.S.; and runs Texas Children’s Urgent Care clinics designed specifically for after-hours pediatric care. In addition, its global health program extends critical care to women and children across the world.

Texas Children’s is affiliated with Baylor College of Medicine. Learn more at www.texaschildrens.org