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Discover the benefits of automated variant annotation for your clinical routine
Automated variant interpretation – fast, precise, efficient MH Guide is an in-vitro diagnostic software approved in Europe. It assists molecular pathologists working with large molecular datasets. Independent of the sequencing technology used, MH Guide can interpret complex datasets and automatically identify genetic variants that are relevant for the treatment of cancer patients. This information is…
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The earlier, the better – turning data into knowledge
Automated analysis of hereditary cancer predispositions Our applications for hereditary cancer predispositions are optimized for automated identification of clinically-significant germline variants associated with hereditary breast and ovarian cancers (HBOC), and other hereditary cancer predispositions.
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基因治療計畫的先驅
將分子學資料轉化為精準醫療MH Guide 是一套分析軟體，輔助病理醫檢師和腫瘤專科醫師解讀龐大的分子學資料集。不論使用何種定序技術，MHGuide 皆能夠有效分析複雜的次世代定序數據，自動識別出與癌症治療有關的基因變異。這些資訊可轉換成臨床知識，協助您規劃個別病患的治療決策。
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Genome-guided treatment decision support for clinical routines
MH Guide is an analysis software that supports molecular pathologists and oncologists in the interpretation of extensive molecular data sets. MH Guide makes complex NGS data sets readable and automatically identifies relevant genetic variants that are important for the treatment of cancer patients. MH Guide summarizes this information in an intuitive analysis report. For this purpose,…
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Unlocking patient care and therapy breakthroughs from biomedical knowledge
Molecular Health is an international biotech IT company based in Heidelberg, Germany, that has been developing innovative software in the field of in-silico and precision medicine since 2004. Molecular Health’s solutions enable the transformation of large amounts of data into evidence-based, clinically relevant decision support tools. They are used where complex data interpretation provides access…
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Pathfinder for genome-based therapy planning
Translate molecular data into precision medicine MH Guide is an analysis software that supports molecular pathologists and oncologists in the interpretation of large molecular datasets. Independent of the sequencing technology used, MH Guide can make complex NGS datasets readable, and automatically identify genetic variants that are relevant for treating cancer patients. This information is translated…
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A good perspective for your individual cancer therapy
For those who expect more Using the MH Guide software, laboratories can analyze the exact characteristics of a tumor. For some patients, these insights may result in additional therapy options, suggestions for adjusting the course of therapy, or recommendations for enrolling in a clinical trial.