Startups
2020
MEDBIOINFORMATICS SOLUTIONS S.L.DISGENET plus can boost your precision medicine and drug R&D applications.
One of the largest catalogs worldwide of genes and variants associated with human diseases, traits and phenotypes.
One of the largest catalogs worldwide of genes and variants associated with human diseases, traits and phenotypes.
Address
Rambla de Catalunya 14, 08007 Barcelona, Spain
CERCA ownership
Barcelona, Spain
1992
Hospital del Mar Research Institute (HMRIB)
CERCA Center Contact
IÁ
Ismael Ávila
Hospital del Mar Research Institute (HMRIB)Other Catalan Public owners
Logo
Status & Deeptech areas
Company Status & Company Deeptech AreasCurrent company status
DeepTech Area
Spinoff information
Company Description
The company aims at exploiting the vast wealth of biomedical data to support drug discovery pipelines and to enhance biomedical research. The company is supported by three pillars: expertise in life sciences, cutting edge methods of artificial intelligence, and vast experience at tackling a variety of biomedical questions.
MedBioinformatics Solutions SL is a spin-off that arises from the joint work of experts from IMIM and UPF. MedBioinformatics Solutions SL has its foundations in the ten years of work of researchers of the Integrated Biomedical Informatics group of the Research Program in Biomedical Informatics of the IMIM and the UPF (GRIB).
MedBioinformatics Solutions SL is a spin-off that arises from the joint work of experts from IMIM and UPF. MedBioinformatics Solutions SL has its foundations in the ten years of work of researchers of the Integrated Biomedical Informatics group of the Research Program in Biomedical Informatics of the IMIM and the UPF (GRIB).
Product description
DISGENET plus: Disease genomics platform to unlock to potential of genomics for drug R&D and health care, containing one of the largest catalogs of genes and variants associated with human diseases, traits and phenotypes. It offers:
Comprehensive knowledge database integrating and standardizing information on disease associated genes and variants.
Coverage of the full spectrum of human diseases as well as normal and abnormal traits, and adverse drug events.
Interoperable resource supporting a variety of applications in genomic medicine and drug R&D.
Comprehensive knowledge database integrating and standardizing information on disease associated genes and variants.
Coverage of the full spectrum of human diseases as well as normal and abnormal traits, and adverse drug events.
Interoperable resource supporting a variety of applications in genomic medicine and drug R&D.