An approch for interpreting disease-associated human variants using single-cell epigenomics

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Author: Gefei Z

Requires: Python >=3.11, <4.0

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Project description

An approach to interpreting disease-associated human variants using single-cell epigenomics

What can sv_var do?

Identify risk genes, gene sets, and cells related to different stages and diseases.

Infer cell types involved in complex traits and diseases using single-cell epigenomes AND does not rely on any other annotations and other Omics data.

Project details

Verified details

These details have been verified by PyPI
Maintainers
Avatar for Gefei from gravatar.com Gefei

Unverified details

These details have not been verified by PyPI

View statistics for this project via Libraries.io, or by using our public dataset on Google BigQuery

Meta

Author: Gefei Z

Requires: Python >=3.11, <4.0

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1.2.2

1.2.1

1.2.0

1.1.0

1.0.0

0.2.6

0.2.5

0.2.4

0.2.3

0.2.2

0.2.1

This version

0.2.0

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