Quality-assured interpretation of complex genetic data

For the growing challenges of today and tomorrow

CE-in-vitro diagnostic software solutions for your data interpretation

Growing data volumes, constantly increasing biomedical knowledge, more complex analytical procedures, and databases that are insufficiently standardized – these are just some of the challenges that molecular pathology and diagnostic laboratories face. In addition, there is time pressure and increasing demands on data interpretation, for example in molecular tumor boards. Our software solutions help you master these challenges more easily.

Better and faster results

With MH Guide, we have developed in-vitro diagnostic software that allows the analysis of genome variants in comparison with the latest scientific findings – efficiently, precisely, and in line with your requirements. MH Guide helps you interpret data and collaborate directly with clinical colleagues.

Precision oncology demands precision pathology

When suitable for patients, precision medicine is increasingly the first-choice cancer treatment. This places increasing demands on molecular pathology and diagnostic laboratories, since targeted cancer therapies require precision pathology to identify appropriate biomarkers in tumor material or liquid biopsy.

MH Guide enables automated gene variant interpretations from small and large panels for evidence-based results with high quality – even at high testing volumes.

Big data analysis for laboratories – automated variant interpretation via “learning database”

MH Guide, one of the first CE-marked IVD medical devices for molecular diagnostics, compares your NGS test results with relevant biomedical knowledge from current research. To do this, the software draws on one of the world’s largest knowledge bases, Dataome, which continuously processes published biomedical knowledge along with information about drugs and current clinical trials.

In addition, MH Guide now makes it easy and time-saving to identify clinical trials that match the patient’s disease, treatment options and location. Results are presented in the same report based on your search criteria (e.g. biomarker, study phase, recruitment status).

Our applications for hereditary cancer support identification and reporting of clinically-significant germline variants associated with hereditary breast and ovarian cancers (HBOC), and other hereditary cancer predispositions.

MH Guide includes a validated process for analyzing NGS data that delivers evidence-based results quickly and comprehensively. This helps your lab increase the quality of result interpretations and simplify report generation – so you are well-equipped to manage all present and future demands that precision medicine entails.

The MH VCF Adapter Suite gives you the ability to adapt output data from different variant detection pipelines to a format compatible with MH VCF via an intuitive stand-alone utility. The MH VCF Adapter Suite includes adapters for Agena, Archer, AmoyDx, Illumina AmpliSeq, Illumina TSO500/TST170, Qiagen and Thermo Fisher Oncomine Comprehensive Assay pipelines and supports a wide range of NGS diagnostic workflows. This helps your laboratory to increase the quality of result interpretations and simplify report generation – so that you are prepared now and in the future for all the demands that the advent of precision medicine brings to patient care.

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How your laboratory benefits

Cloud-based portal

Fast login and quick access to the latest platform version

Rapid results

High-speed clinical annotation and report creation

Simple upload

Easily upload files via encrypted connections

Trusted

Our annotations undergo a rigorous review process

Secure

Data processing in accordance with GDPR, state-of-the-art encryption

Scalable

Review as many variants as you find useful

Platform-independent

Accepts standard file formats from any analysis method

Affordable

Single and volume pricing available

MH VCF Adapter Suite

Adapt output data from various variant detection pipelines to a format compatible with MH VCF using this intuitive stand-alone utility. The MH VCF Adapter Suite includes adapters for Agena, Archer, AmoyDx, Illumina AmpliSeq, Illumina TSO500/TST170, Qiagen and Thermo Fisher Oncomine Comprehensive Assay pipelines and supports a wide range of NGS diagnostic workflows.

The workflow of MH Guide

How your lab benefits:

Efficient, high-quality results

“Increasingly, larger panels are playing a role in molecular testing and variant interpretation. Automated interpretation tools like MH Guide ensure fast and accurate results.”  

We have put together a brochure for you to find out more about the benefits and functionality of MH Guide.

Dr Jochen Theis

Jochen Theis, MD PhD
Acting Chief Medical Officer
Head of Business Unit AI Pharma Solutions

FAQs

We would be happy to offer you a software demo. Send us your request in writing or call us: +49 6221 43851-150.

MH Guide can process FASTQ and VCF data and offers pathologists highly-automated generation of individual patient reports, each of which can be expanded and refined, including results from non-NGS methods (FISH, IHC, (q)PCR). The software generates well-designed, adaptable report templates in various formats (PDF, JSON, XML).

MH Guide fulfills the highest standards in terms of data privacy and data protection, as well as risk and quality management. Data sovereignty always lies with the user. Confidential patient data is transmitted and stored using advanced encryption standards (SSL/TLS, AES-256).

This depends on your requirements. Prices are calculated based on the number of analyses and the size of the gene panels to be analyzed. We are happy to advise you personally.

You can use any commercial or proprietary gene panel (small or large) and have the data analyzed in VCF format with MH Guide. Likewise, whole-exome (WES) and whole-genome (WGS) data can be analyzed with MH Guide. Raw data (FASTQ) from gene panels and WES analyses from popular Illumina platforms can be analyzed using MH Guide Premium.

MH Guide allows users to maintain and edit their own annotation data and variant classifications in a personal, secure account area. On request, Molecular Health can assist you in transferring ACMG-compatible variant classifications and descriptions from your own databases to your account.

Yes, you can assign case-related accounts and rights, giving clinical colleagues access to the discussed case.

Our software solutions for the optimal support of laboratory decisions

For solid and ​ hematologic cancers​

The comprehensive application for automated interpretation of NGS data from any kind of solid or hematologic cancer
MH Guide quickly and accurately identifies and interprets genetic variants in cancer. The MH Guide report helps treatment providers choose therapy options and clinical trials that match the cancer patient’s molecular profile.
Find out more

For hereditary cancers​

Comprehensive applications for automated interpretation of NGS data from hereditary cancers
Our applications support you in identifying clinically-significant germline variants associated with hereditary breast and ovarian cancer syndrome (HBOC), or other hereditary cancers.
Find out more
Dr. Daniel Kritsch

Dr. Daniel Kritsch
Senior Application Specialist – Scientific Field Support

“We are working to identify clinically-relevant gene variants as efficiently and reliably as possible. Our goal is to give you the best possible support for your daily analyses and your research projects.”

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