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A Snakemake workflow to split, filter, normalize, integrate and select highly variable features of count matrices resulting from experiments with sequencing readout (e.g., RNA-seq, ATAC-seq, ChIP-seq, Methyl-seq, miRNA-seq,...) including diagnostic visualizations.

Home Page: https://epigen.github.io/spilterlize_integrate/

License: MIT License

Python 65.60% R 34.40%
atac-seq batch-effect chip-seq count-matrix dimensionality-reduction integration ngs normalization rna-seq bioinformatics

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spilterlize_integrate's Issues

Duplicate rows in input

Does not catch the error of getting input dataframe with duplicate gene/feature names till filter_features rule.

add example data and configuration

either from tutorials e.g., limma or wait until other modules are ready for one test that goes from SRA download until enrichment analysis -> this will produce example data for most modules.

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