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Efficiently and precisely annotating genetic variants in a clinical context – with Molecular Health Guide

How diagnostic and pathological labs can benefit from software-aided interpretations in the field of personalized cancer treatment

Labs

Efficiently and precisely annotating genetic variants in a clinical context – with Molecular Health Guide

How diagnostic and pathological labs can benefit from software-aided interpretations in the field of personalized cancer treatment

Clinical annotation as the standard in personalized cancer treatment — a challenge in oncological pathology

Precision medicine is making great advances, especially in the field of oncology. Even though there are many variant-analyses panels on the market, clinically annotating and interpreting these variants comprehensively remains a difficult topic for physicians.

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Big data analytics for laboratories – using MH Guide to systematically and safely perform knowledge-based clinical annotations

MH Guide is the first certified medical device in Europe in this diagnostic field to create a context between test findings and the relevant biomedical knowledge from current research. Furthermore, it takes the respective patient’s clinical parameters into account and summarizes findings in a report that provides the maximal information possible. This enables the treating physician to prioritize therapeutic options for the given tumor profile as well as suggest appropriate clinical trials.

MH Guide includes a validated process for analyzing NGS data to provide comprehensive and fast evidence-based results. This helps your lab increase the quality of the interpreted findings and expedite the diagnosis so that now and in the future, you will be prepared for all of the demands that will arise as precision medicine makes its way into oncology.

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Simple cloud-based portal

Quick login & access to latest platform version

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Delivers results quickly

Industry-leading speed for clinical annotation and report generation

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Simple

Simple upload of data file via sFTP secure procedure

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Trustworthy

Our annotations undergo a rigorius review process

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Secure

HIPPA compliant and industry-standard data encryption

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Scalable

Review as many variants as you deem useful

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Platform agnostic

Accepts standard file formats (like VCF or XML), regardless of analytical methods

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Affordable

Individual and volume pricing available

How your lab can benefit from the use of MH Guide

You can handle larger volumes of sequencing data more precisely and extensively with the help of our genomic analysis pipeline

 

You will generate quality-assured clinical variant annotations more quickly


You can optimize therapeutic options for treating physicians and their patients, thus creating an indisputable added value for your lab and your customers

You will become part of the future market of personalized medicine



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How your lab can benefit from the use of MH Guide

You can handle larger volumes of sequencing data more precisely and extensively with the help of our genomic analysis pipeline

 

Molecular Health Button

You will generate quality-assured clinical variant annotations more quickly



Molecular Health Button

You can optimize therapeutic options for treating physicians and their patients, thus creating an indisputable added value for your lab and your customers


Molecular Health Button

You will become part of the future market of personalized medicine



Molecular Health Button

Our powerful applications for treatment decision support


Molecular Health Guide (MH Guide) identifies safe and effective therapies for patients by analyzing the molecular profile. It matches detected mutations to the world’s knowledge in the field of oncology and hereditary diseases and helps medical experts to create a patient-specific clinical report. MH Guide is an IVD registered in the EU.




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Molecular Health Guide Mendel (MH Mendel) supports human geneticists to identify clinically significant genetic variants and create a diagnostic report for individual patients.   

MH Mendel is part of the Molecular Health Guide (MH Guide) solution which is an IVD registered in the EU. 





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Molecular Health Guide BRCA (MH BRCA) supports medical professionals in identifying and reporting clinically significant germline variants associated with hereditary breast and ovarian cancer (HBOC) syndrome from NGS-based assessment of BRCA1 and BRCA2 and other HBOC related genes. MH BRCA is part of the Molecular Health Guide (MH Guide) solution which is an IVD registered in the EU.


Become a partner laboratory now!

Does our solution appeal to you? Would you like to become an MH partner? We look forward to hearing from you.

EU: +49 6221 43851-150
E-Mail: CustomerCareEU@molecularhealth.com

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Let’s talk about how our technology can work for you

To find out more, you can call our customer care team or help desk or send us an e-mail. We would be delighted to provide you with more information or answer your questions.


EU: +49 6221 43851-150
E-Mail: CustomerCareEU@molecularhealth.com