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These are just a few suggestions I have that may help with the README.
Add a license badge.
Improve the description
Add links in the description to those tools and not that DITTO will be published or is being written
Add a screenshot of the app
Explain or mention before showing screenshot or after what can you search for: by gene? by variant? all?
I'd be happy to help here or review if needed.
A potential description
The DITTO web application offers a scientific platform for researchers to investigate deleterious variants, combining the DITTO deleteriousness score and ClinVar's reported significance to comprehensively assess variant impact.
DITTO uses an explainable neural network model enhanced by SHAP for transparent model predictions, ensuring clarity in understanding the functional implications of variants. It is rigorously trained with ClinVar data and integrates OpenCravat for detailed annotations from diverse sources.
The application is a reliable resource for [who is this tool for], providing a transparent, score-based system to evaluate the potential deleterious effects of genetic variants, aiding in precise and informed research decisions.
The text was updated successfully, but these errors were encountered:
These are just a few suggestions I have that may help with the README.
I'd be happy to help here or review if needed.
A potential description
The DITTO web application offers a scientific platform for researchers to investigate deleterious variants, combining the DITTO deleteriousness score and ClinVar's reported significance to comprehensively assess variant impact.
DITTO uses an explainable neural network model enhanced by SHAP for transparent model predictions, ensuring clarity in understanding the functional implications of variants. It is rigorously trained with ClinVar data and integrates OpenCravat for detailed annotations from diverse sources.
The application is a reliable resource for [who is this tool for], providing a transparent, score-based system to evaluate the potential deleterious effects of genetic variants, aiding in precise and informed research decisions.
The text was updated successfully, but these errors were encountered: