gnomAD variant frequencies by study
Is there a way to extract variant frequencies by study from gnomAD? By default, they break it up by population.
A lot of gnomAD data comes from disease-specific projects. For example, they use TCGA data. It would nice to see the breakdowns of TCGA versus non-TCGA, or by TCGA cohort. Is that possible? If not, is there maybe another resource that does that?
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