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This is a very brief description that we'll need to flesh out more, particularly with help from @gwaygenomics:
Cognoma will provide the opportunity to construct a supervised machine learning model that predicts a feature of interest. For example, mutations of genes in a specific pathway.
We anticipate that this endpoint will allow the user to specify a set of genes and samples. The endpoint would return the number of samples that contain alterations within that set.
The text was updated successfully, but these errors were encountered:
I think this step is where the user will start. They will have the option to input their own list of genes or the option to be assisted by @dhimmel's hetnets. There should also be options to filter mutation types depending on expected pathogenicity.
This step should inform the tissue/sample selector and give suggestions based on tissues relevant to the query.
This is a very brief description that we'll need to flesh out more, particularly with help from @gwaygenomics:
Cognoma will provide the opportunity to construct a supervised machine learning model that predicts a feature of interest. For example, mutations of genes in a specific pathway.
We anticipate that this endpoint will allow the user to specify a set of genes and samples. The endpoint would return the number of samples that contain alterations within that set.
The text was updated successfully, but these errors were encountered: