Labs | Molecular Health

Laboratories

Analyzing and reporting NGS data (DNA, RNA) quickly, easily, and accurately

Diagnostic and pathological NGS labs can benefit from software-aided interpretations in the field of personalized cancer treatment and genetic phenotype interpretation

Laboratories

Analyzing and reporting NGS data (DNA, RNA) quickly, easily, and accurately

Diagnostic and pathological NGS labs can benefit from software-aided interpretations in the field of personalized cancer treatment and genetic phenotype interpretation

Genomic variant detection and interpretation by labs

Interpreting genomic variants from NGS sequencing data is a growing challenge, as the knowledge about the significance of genetic variants, both from a medical perspective and in the context of phenotype interpretation, is constantly increasing. We solve this by offering Molecular Health Guide with its components MH Guide, MH Mendel, and MH BRCA. 

Read more about this in our Products section

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High-throughput solutions with built-in biomedical content

Molecular Health Guide (including MH Guide, MH Mendel, and MH BRCA)  is a fast, easy way for NGS labs to access the Molecular Health database of medically and scientifically curated, peer-reviewed and published evidence to generate a summary of potentially effective and ineffective medications, as well as medications that may pose a higher risk of adverse reactions or cancer progression.

 

The software creates a complete genetic profile and a list of associated phenotypes, so your laboratory can serve clinicians, hospitals, and human geneticists. The MH Guide platform comes with a rich set of software and data features to run an NGS laboratory at very low cost.

 

Molecular Health Guide is platform-agnostic, so it easily integrates with your current workflow and platform.

Gaining insights has never been easier

Over the last decade, Dataome has grown to become one of the largest globally available resources of clinico-molecular data and knowledge. From millions of patient lives to hundreds of billions of molecular data points, it provides a single point of access to the world’s biomedical knowledge through our decision support applications.

 

Molecular Health Guide (MH Guide) identifies safe and effective medication for cancer patients by analyzing the cancer’s molecular profile. It matches detected tumor mutations to the world’s knowledge in the field of oncology and helps medical experts to create a patient-specific clinical report with treatment recommendations.

 

 

Molecular Health Guide Mendel (MH Mendel) supports human geneticists in diagnosing hereditary diseases and creating diagnostic reports for individuals. The germline data analysis follows official genetic guidelines and uses the latest, world known ACMG variant classification criteria.

 

 

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Molecular Health Guide BRCA (MH BRCA) supports medical professionals in identifying and reporting clinically significant germline variants for hereditary breast and ovarian cancer.  It creates individual patient reports based on NGS data from BRCA1/BRCA2 and other associated genes following official genetic guidelines. 

 

Become a partner laboratory now!

We are looking for lab partners to serve our hospitals with sequencing services. We look forward to hearing from you.

E-Mail: CustomerCareUS@molecularhealth.com

Our lab partners

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Let’s talk about how our products can work for you.

Call us for a product demo and learn how to broaden your lab portfolio while lowering costs.

Phone: +1 346-221-1955

E-mail: CustomerCareUS@molecularhealth.com