Entering edit mode
4.0 years ago
b.mascat
•
0
Hello everyone,
I have a total of 60 publications with cohorts of differen size (from one single case report to cohort studies). I want to ETL the informattion about the causal mutations in each patient and his corresponding phenotype. Exist any tool, package or pipeline to do this effienctly?. Review each paper and anotate this features manually it is not a option.
