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SC-VAR

Here we report a human variants interpreter, named SC-VAR.

What can sc-var do?

This tool can interpret disease-related risks with whole genome wide (including both coding and non-coding regions) variants from GWAS studies and single-cell data on four layers: risk CREs,risk genes, gene sets, and cell types.

How to install?

pip install sc-var

About

Fig1

Usage

Check https://github.com/gefeiZ/sc_var/tree/main/Vignettes for details

Data request:

Single cell data &

Peak co-accessibility Data or Peak to gene linkage Data (which could obtained from single cell data using cicero or signac) &

GWAS data

Metadata

Release files for sc-var 1.3.0

For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.

Source distribution (sdist)

Source distribution for sc-var 1.3.0
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Table of built distributions (wheels) for sc-var 1.3.0
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sc_var-1.3.0-py3-none-any.whl Python 3 none any Details

Total release size: 22.0 kB

Release files / sc_var-1.3.0.tar.gz

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