Genetics | Media Room | Newswire

Publication of Landmark Study in JACC: Advances

Tue, 28 Oct 2025 15:45:00 +0000

CARDIO inCode-Score Genetic Risk Influences Cholesterol Risk and Prediction of Coronary Heart Disease

PharmaNest, NIH and VCU Launch Confirmatory Retrospective Outcome Study With 1,765 Patients to Advance AI-Driven Digital Pathology in MASLD

Thu, 11 Sep 2025 21:00:00 +0000

PharmaNest Inc. announced today a multi-institutional research collaboration with Virginia Commonwealth University (VCU) and the National Institutes of Health (NIH) to confirm the prognostic performance of artificial intelligence (AI) powered digital pathology biomarkers in metabolic dysfunction-associated steatotic liver disease (MASLD) in a retrospective cohort of 1,765 patients with MASH (NASH CRN DB2 Cohort)

AmplifyBio Drives Key Conversations at Phacilitate's Advanced Therapy Week in Dallas

Thu, 30 Jan 2025 12:00:00 +0000

Hyris Technology Supports the Fight Against One of the World’s Deadliest Diseases, Malaria

Tue, 20 Feb 2024 08:00:03 +0000

Hyris’ molecular diagnostic technology has been adapted to enable real-time surveillance of mosquito vector insecticide resistance, which will aid in malaria control campaigns.

Basepaws Launches the Most Extensive DNA Test for Dogs, Focused on Health and Early Detection of Disease Risk

Fri, 06 Oct 2023 12:00:00 +0000

Hyris Supports Researchers and Developers to Launch Testing Kits via New Onboarding Programs

Wed, 27 Sep 2023 09:00:02 +0000

Following the launch of its Marketplace in 2022, Hyris continues to leverage the AI capabilities of its genetic testing platform, renowned for its adaptability, to support both researchers and kit developers worldwide. New onboarding programs enable emerging players to accelerate their go-to-market, as well as established manufacturers and diagnostic providers to integrate their portfolio with ease, maximizing their cost-per-value strategy.

In Collaboration With JScreen, Cancer Warrior Lainie Jones Advocates for Genetic Testing

Tue, 22 Aug 2023 17:30:02 +0000

Plant Sciences, Inc. Unveils Restructuring, Broadening North American Growers' Access to Its Diverse Berry Variety Portfolio

Tue, 01 Aug 2023 14:00:10 +0000

FamilieSCN2A Foundation Announces Inaugural $2.5M Hodgkin-Huxley Research Award

Tue, 09 May 2023 13:00:18 +0000

Yang Yang, PhD, of Purdue University is the recipient of a major 5-year grant for Personalized Treatment Development in SCN2A-Related Disorders

Charcot-Marie-Tooth Association: Sperm Donor With CMT Gene Passes It on to Multiple Families

Tue, 09 May 2023 11:00:07 +0000

A New T-Cell activation assay based on Hyris qPCR Technology marks a disruptive approach for the detection of SARS-CoV-2 specific cellular immunity

Wed, 15 Jun 2022 12:00:05 +0000

A scientific paper recently published in Nature Biotechnology reveals new research regarding how we track and monitor T-cell patients' immunity to SARS-CoV-2, leveraging the unique characteristics of Hyris System™. The study results from a joint effort of an international research team from the Icahn School of Medicine at Mount Sinai, Singapore Duke-NUS Medical School, laboratory diagnostic service providers Synlab, and Hyris.

LifeBank Chain Brings Ultimate Gene and Cell Therapy Benefits to Everyone

Wed, 12 Jan 2022 16:00:03 +0000

LifeBank Chain (LBC) focuses on genetics and cell research, with the purposes of furthering human longevity and expanding access to genetics and cell treatments.

Vilcek Foundation Opens Applications for the 2022 Creative Promise Prizes in Biomedical Science

Mon, 01 Mar 2021 16:45:00 +0000

Three prizes of $50,000 will be awarded to early-career immigrant research scientists

Genetic Testing at Home

Fri, 30 Oct 2020 13:00:00 +0000

From Cultural Curiosity to Health Necessity in COVID

Genome Editing Market Revenue to Cross USD 10 Bn by 2026: Global Market Insights, Inc.

Mon, 05 Oct 2020 08:00:00 +0000

Asia Pacific genome editing market will showcase growth of 15% during the forecast period owing to increasing number of genetic research organizations in emerging economies that are working on the development of innovative gene-editing tools.

Diagnomics Introduces HealthLytix Alzheimer's Disease Risk Assessments Through GenoMatch.Me Employee Benefits Program

Wed, 12 Feb 2020 15:00:00 +0000

BillionToOne, Inc. and Eluthia Launch UNITY™ Test, the First Non-Invasive Prenatal Test for Cystic Fibrosis, Spinal Muscular Atrophy and Hemoglobinopathies in Germany, Austria, Switzerland and the Netherlands

Thu, 31 Oct 2019 18:09:00 +0000

BillionToOne and Eluthia have announced today the launch of the first and only non-invasive prenatal test, allowing to screen for the autosomal-recessive conditions cystic fibrosis, spinal muscular atrophy (SMA), sickle cell disease and other hemoglobinopathies. The UNITY™ screen will be made available through Eluthia in Germany, Austria, Switzerland, and the Netherlands, as of now.

Landmark Study Seeks Participants With VCFS-Related Psychosis to Help Create Biobank of Human Neural Tissue to Develop Innovative Treatments

Wed, 23 Oct 2019 13:00:00 +0000

The Virtual Center for Velo-Cardio-Facial Syndrome collaborates with the Center for Precision Neuropsychiatry based in the Department of Psychiatry at Columbia University Vagelos College of Physicians and Surgeons

Diagnomics Releases Cardiovascular Health Panel on Clinical Microarray Platform

Mon, 07 Oct 2019 14:00:00 +0000

Diagnomics Added CLIA Certificates From Maryland, Pennsylvania, and Rhode Island

Mon, 09 Sep 2019 14:00:00 +0000

Dante Labs Launches GenomeL, the First Commercial Long Reads Human Whole Genome Sequencing

Mon, 08 Apr 2019 14:00:00 +0000

Dante Labs introduced 30x long reads whole genome sequencing based on Oxford Nanopore technology. This is the first long reads whole genome available commercially worldwide. Sequencing will be performed at Dante Labs' new highly automated, certified third-generation sequencing center in L'Aquila, Italy.

Diagnomics Introduces ACMG 59 Reports for Personalized Genetic Testing

Thu, 17 Jan 2019 22:12:00 +0000

FORMULATRIX® Digital PCR Technology to Be Acquired by QIAGEN

Mon, 14 Jan 2019 02:04:00 +0000

Diagnomics Partners With Translational Software to Launch Pharmacogenetic Testing Services in the United States

Mon, 15 Oct 2018 11:00:00 +0000

Partnership offers PGx solutions on advanced genotyping array to enable precision medicine

Dante Labs Expands Its Full DNA Test With Proprietary Analysis of Mitochondrial and Neurological Diseases

Wed, 10 Oct 2018 15:48:00 +0000

Color Partners With Sayre Therapeutics to Provide Access to Affordable Hereditary Cancer Assessment Tests in India

Wed, 18 Jul 2018 05:00:00 +0000

The Color-Sayre partnership will provide a fully integrated solution for patients and providers by delivering actionable clinical test results at an accessible price point.

Dante Labs Launches Whole GenomeZ, a New Whole Genome Sequencing Technology for Advanced Diagnostics

Wed, 11 Jul 2018 12:00:00 +0000

Dante Labs introduced a new Whole Genome Sequencing of 130X coverage for the Exome and 30X coverage for DNA's non-coding regions

Xcode Life Announces the South Asian Genome (SAGE) Project

Sat, 23 Jun 2018 10:00:00 +0000

Promotional offer: Free Xcode Ancestry report for all eligible individuals

X Genomics Unlocks Life Sciences Putting Big Human Genetic Data on the Blockchain

Fri, 25 May 2018 00:00:00 +0000

Baby Genes, Inc. Receives Accreditation From College of American Pathologists (CAP)

Thu, 24 May 2018 10:00:00 +0000

CAP Accreditation is Awarded to Clinical Laboratories Meeting the Highest Standards in Quality Laboratory Practices

Rainbow Genomics and Color Genomics Team Up to Provide Access to Affordable Hereditary Cancer and Heart Health Genetic Risk Assessment Tests in Asia

Wed, 23 May 2018 13:54:00 +0000

Partnership combines local support with global capabilities to deliver affordable tests to identify genetic mutations associated with an increased risk for hereditary cancer and inherited heart conditions for which early knowledge can make a difference.

Decoding Human Health: How One Partnership is Bringing Accessibility and Collaboration to Genomic Data Analysis

Thu, 03 May 2018 13:00:00 +0000

Two U.S. BioTechs partner to unlock more data discovery in genomics, creating first end-to-end analysis engine simplified for researchers

An NGS Approach for Research on the Genetic Determinants of Female and Male Infertility, New Webinar Hosted by Xtalks

Fri, 20 Apr 2018 12:00:00 +0000

Comprehensive Interrogation of the Genetic Determinants of Female and Male Infertility: A New NGS Research Application Enabled by Improvements in Target Enrichment Technology

Ehlers-Danlos Society Receives Transformational Gift for Genomic Research Into Rare Disorder, HyperMobile EDS

Tue, 13 Feb 2018 22:58:00 +0000

Anonymous donor presents $1 million gift to The Ehlers-Danlos Society to jumpstart groundbreaking genomic research into genetic cause of hypermobile Ehlers-Danlos syndrome (hEDS), a rare, degenerative, and all-too-often painful, disabling connective tissue disorder

ExploringLifesMysteries.com Announces Annual Best DNA Test Reviews Winners

Tue, 14 Nov 2017 14:00:00 +0000

DNA industry experts help consumers make best decision this holiday season with unbiased analysis of the leading DNA test companies

HumanCode Appoints Dr. Carlos Bustamante to Scientific Advisory Board

Wed, 18 Oct 2017 17:36:00 +0000

Strand Life Sciences Announces the Release of Strand NGS v3.1 at ASHG 2017

Tue, 17 Oct 2017 20:42:00 +0000

Strand NGS now supports large scale RNA- and small-RNA-Seq and Unique Molecular Identifiers (UMIs) for DNA-, RNA-, and small-RNA-Seq.

Breakthrough CRISPR/Cas9 Rat Model Technology

Tue, 17 Oct 2017 10:22:00 +0000

Announced by ingenious targeting laboratory

New Research Reveals Genetic Engineering Strategies for Elevating Human Consciousness

Mon, 16 Oct 2017 05:00:00 +0000

Personalized Lifestyle Medicine Conference Brings Healthcare Professionals to Seattle in October

Tue, 10 Oct 2017 21:18:00 +0000

HumanCode Gives Couples a DNA-Based Glimpse Into Their Future Children

Tue, 03 Oct 2017 13:00:00 +0000

BABYGlimpse, a new app available on the Helix marketplace, explores over 20 different traits, including ancestry, physical appearance, and wellness-related traits

Mental Health News Radio Network Announce Strategic Sponsorship by MyGenetx to Promote Public Knowledge About Pharmacogenetics

Thu, 28 Sep 2017 05:28:00 +0000

Bringing mental health professionals and genetic scientists together.

Baylor Genetics Partners With Rainbow Genomics Offering Adult Wellness Screening and High-Risk Cancer Exome Sequencing Tests in Asian Pacific

Mon, 25 Sep 2017 16:11:00 +0000

Baylor Genetics Partners With Rainbow Genomics

New Study Helps Solve a Great Mystery in the Organization of Our DNA

Thu, 18 May 2017 16:00:00 +0000

Discovery at Gladstone Institutes will help reevaluate the cause of certain cancers and developmental defects

LGS Foundation Announces New Partnership With CURE's Epilepsy Genetics Initiative (EGI) Program

Thu, 16 Mar 2017 13:00:00 +0000

Thu, 10 Nov 2016 21:00:00 +0000

June 12 - 18 2016 Is Rare Chromosome Disorder Awareness Week

Mon, 13 Jun 2016 16:07:42 +0000

HungryBot App Recognizes Your Food From Photographs, Helps Researchers Study Disease

Thu, 19 May 2016 16:48:48 +0000

Avid Entrepreneur Launch Comprehensive Platform on American Genealogy

Fri, 22 Apr 2016 20:39:10 +0000

Rombergers Marking 263 Years in the U.S.

Sat, 09 Apr 2016 18:20:21 +0000

On June 18th, Berrysburg's historic Hill Church provides a bucolic backdrop to the Romberger All-Family Reunion where friends, food, fun and genealogy rule. Descendants of Bartel, the original immigrant ancestor for American Rombergers (and variations) meet once more to share info, make new family friends, and celebrate the life of the family association founder, Dr. John Romberger.