Finding mechanistic
clues in data
Disease and trait signature gene discovery, multi-omics integration, diagnostic, prognostic and subtyping models, and independent cohort validation.
Connecting public data, multi-omics evidence and biological mechanism around your scientific question.
Disease and trait signature gene discovery, multi-omics integration, diagnostic, prognostic and subtyping models, and independent cohort validation.
Species-, disease- and topic-specific databases, knowledge graphs, and visual query and online analysis platforms.
Drug prediction, batch molecular docking, virtual screening and molecular dynamics, giving computational support to target and candidate molecule research.
Ordered as the first five items of the catalogue's "disease/trait signature genes & mechanisms"; each step can also stand alone.
Combine transcriptome, proteome and metabolome data to find genes tied to a disease or trait.
Related servicesDiagnostic, prognostic or subtyping models from the signature genes.
Related servicesUse single-cell data to see in which cells and processes the signature genes act.
Related servicesCMap / LINCS to look for drugs that may reverse the disease expression signature.
Related servicesTest the conclusions in independent cohorts or experimental data.
Related servicesWithout new sequencing, data can be downloaded from public databases and reanalysed to find new questions.
See public data mining services15 kinds of topic databases and online platforms in the catalogue. Select any one to start a research brief.
Specialized databases, disease/trait mechanisms and single-cell integration: 53 services in total.
Tell us about your research and your data, and find the next step together.