Exploring the connectivity between observational data and molecular networks
Pitch
Objective of this hackathon to explore to what degree is possible to build a Knowledge Graph spanning observational data to molecular data.
From a standardised representation of a patient record (e.g.: in OMOP) we can derive observations (diagnosis, phenotypes, biomarkers). At a molecular level, we have a range of resources in terms of protein-protein interaction networks or pathways that can explain how some molecular alterations are causally connected. Linking these two levels, we have gene-to-diseases associations, but also potentially phenotype databases or more.
To what degree is it possible to formulate a holistic network such that, given a range of patient level observations, it would be possible to trace them to the alteration of connected molecular mechanisms?
To what degree it would be possible to characterise a patient in terms of overall pathways/networks affected?
Objective of this hackathon are:
To assess what data resources are available, what is publicly available or not.
To assess how much such data resources can be connected or not, in terms of using common ontologies
To assess the coverage and sparsity of such connections
To assess how much an overall graph would be informative, given the high level of abstraction (e.g.: many statements on molecular networks are de-contextualised respect to tissue or individual characteristics)
This is an explorative hackathon. The outcome is a better understanding on what is available, gaps, potential and limitations in building a KG spanning population-to-bench data.
Expertice needed
Any knowledge of:
Databases resources available covering: patients data (incl. synthetic), diseases, phenotypes, symptoms, pathways, p-p interactions or any other relevant data source.
Experience in developing or using integrating knowledge graphs (e.g.: Neurocommons, Dissent, Linked-Life data,...)
Some technical expertise to quickly explore and extract patterns from datasets
Some biomedical expertise to assess the quality/feasibility of the information found
Short title
Exploring the connectivity between observational data and molecular networks
Pitch
Objective of this hackathon to explore to what degree is possible to build a Knowledge Graph spanning observational data to molecular data.
From a standardised representation of a patient record (e.g.: in OMOP) we can derive observations (diagnosis, phenotypes, biomarkers). At a molecular level, we have a range of resources in terms of protein-protein interaction networks or pathways that can explain how some molecular alterations are causally connected. Linking these two levels, we have gene-to-diseases associations, but also potentially phenotype databases or more.
To what degree is it possible to formulate a holistic network such that, given a range of patient level observations, it would be possible to trace them to the alteration of connected molecular mechanisms?
To what degree it would be possible to characterise a patient in terms of overall pathways/networks affected?
Objective of this hackathon are:
This is an explorative hackathon. The outcome is a better understanding on what is available, gaps, potential and limitations in building a KG spanning population-to-bench data.
Expertice needed
Any knowledge of: