Logo

clinical decision support

VieCure, Exact Sciences Partner to Ease Genomic Testing Access, Interpretation

The AI-based decision support firm will integrate Exact's tests into its clinical care management tool, aimed at community oncologists.

PGx Testing Reduces Adverse Drug Events, Multi-Site European Study Finds
Premium

The three-year Ubiquitous Pharmacogenomics Consortium's PREPARE study enrolled nearly 7,000 patients in seven European countries.

Ampel BioSolutions, Duke Researchers Establish Fibromyalgia Gene Signature
Premium

Ampel will use the signature to develop FibroGene, a fibromyalgia blood test that the company expects to launch next year.

UCSF Health Set to Launch Clinical Pharmacogenetics Program
Premium

Doctors will be able to test patients for 17 genes known to influence response to 62 drugs and receive guidance from EHR-embedded pre- and post-test alerts.

Labcorp, VieCure Collaborate on NGS, Software for Cancer Diagnosis

Startup oncology bioinformatics firm VieCure expects this collaboration to bring precision oncology diagnostics and treatment to more community clinics.

Jan 4, 2023

Standards, Regulation, Funding Move Bioinformatics in 2022, But Hurdles to Precision Medicine Remain
Premium

Dec 16, 2022

EU Awards €4.8M to Support Transition of NGS Workflows to Clinical Settings
Premium

Dec 14, 2022

NewStem, MSK Innovation Hub Team to Validate Cancer Diagnostics Software Platform

Dec 7, 2022

Intermountain Builds Up Bioinformatics to Make HerediGene Sequencing Data Clinically Actionable
Premium

Nov 11, 2022

At AMIA, Clinical Decision Support Called Key to Wider PGx Use, Greater Efficacy
Premium

Oct 31, 2022

Genomic Testing Cooperative Implementing AI, Molecular Profiling to Improve Cancer Diagnosis
Premium

Oct 25, 2022

Nest Genomics Building EHR-Integrated Clinical Decision Support for Genetics-Informed Care
Premium

Oct 14, 2022

Clinical Decision Support Guidance Suggests FDA Will Regulate Risk Scores, Treatment Recommendations
Premium

Sep 21, 2022

Sophia Genetics Partners With MSK on Clinical Decision Support, Boundless Bio on ecDNA Detection

Sep 1, 2022

Ampel BioSolutions Enters MDx Market With Lupus, Dermatology Gene Expression Assays
Premium

Aug 24, 2022

Myriad Genetics, Clarified Precision Medicine Team up on Molecular Tumor Board Service

Aug 4, 2022

GenomOncology, Congenica Team up to Develop Precision Oncology Dx Platform

Aug 2, 2022

Genomenon to Curate Genes for Rady Children's BeginNGS Newborn Screening Panel

Jul 20, 2022

Molecular Health Gains EU IVDR Certification for Clinical Decision Support Software

May 25, 2022

Centogene Gets CE-IVD Mark for Cloud-Based Genetic Diagnostics Software Platform

May 18, 2022

BC Platforms, Euformatics, Oncompass to Develop Oncology NGS Workflows for European Hospitals

May 11, 2022

SAS, BC Platforms Partnership Expected to Open New Markets, Improve Data Integration
Premium

May 11, 2022

Sophia Genetics Says New Product May Boost 2022 Revenues, Provides Project Updates
Premium

Apr 13, 2022

Meditech Installs EHR Genomics Add-on at Health Systems in Pursuit of Precision Medicine
Premium

Apr 13, 2022

Mayo Clinic Study Bolsters Implementation of PGx Data in Clinical Practice
Premium

Breaking News
The Scan

Cell Signaling Pathway Identified as Metastasis Suppressor

A new study in Nature homes in on the STING pathway as a suppressor of metastasis in a mouse model of lung cancer.

Using Bees to Gain Insights into Urban Microbiomes

As bees buzz around, they pick up debris that provides insight into the metagenome of their surroundings, researchers report in Environmental Microbiome.

Age, Genetic Risk Tied to Blood Lipid Changes in New Study

A study appearing in JAMA Network Open suggests strategies to address high lipid levels should focus on individuals with high genetic risk and at specific ages.

Study Examines Insights Gained by Adjunct Trio RNA Sequencing in Complex Pediatric Disease Cases

Researchers in AJHG explore the diagnostic utility of adding parent-child RNA-seq to genome sequencing in dozens of families with complex, undiagnosed genetic disease.