DISGENET: The most complete genomics platform - Home
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Unleash your research with the world's most reliable and extensive gene-disease association network.

F-score 92% | 50M+ associations | Cited in 6.500+ papers

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Accessing reliable and up-to-date biomedical data is becoming more and more challenging

Many databases exist and scientific literature keeps growing, but this doesn't solve the problem of data access
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Scattered biomedical data across various databases and repositories creates data silos, hindering accessibility for crucial research.

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A wealth of data on genes, variants and diseases exists, but incompatible formats and terminology create barriers to analysis.

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100,000+ disease genomics articles are published each year, causing slow updates and incomplete data in curated databases.

DISGENET integrates all genes and genomic variants information into a single resource

Use case: Unlock precision medicine opportunities

Sequencing an individual's genome can produce a vast amount of data, with millions of genomic variants identified. However, pinpointing which of these variations actually contribute to disease remains a major hurdle in precision medicine.
Challenge

Solution

Benefits

DISGENET is a knowledge database that covers the full spectrum of human diseases so you can:

Streamline Your R&D Process
Expedite the search for relevant information

DISGENET's cutting-edge AI and NLP technology extracts the most relevant information with exceptional accuracy, saving you time and resources during the crucial early stages of drug discovery.

Identify Novel Drug Targets
Leverage unseen connections

DISGENET enables you to identify novel drug targets by uncovering previously hidden connections. Explore promising new avenues for therapeutic interventions and accelerate the development of life-saving treatments.

Drive Precision Medicine Forward
Advance personalized treatments

DISGENET's standardized data integration unlocks new possibilities in precision medicine. Develop more effective and targeted therapies tailored to specific patient populations based on their unique genetic makeup.



What do customers and researchers say about DISGENET?

When exploring the DNA methylation of Cri du Chat patients, DISGENET helped me find interesting connections between genes with DNA methylation changes in the promoter and disease phenotypes. This analysis was suggestive of the DNA methylation itself having a role in developing the characteristics of this understudied rare disease.

Petter Holland - PhD, Researcher at Oslo University Hospital, Norway

Article


Dedicated to supporting academic research

Are you a student, academic or not-for-profit researcher who wants to access the latest biomedical data?
Unlock the full potential of your research with DISGENET's dedicated academic plans.
DISGENET is built by researchers from academic institutions

Read the latest articles on our Blog


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