Genomic data normalization software to standardize and remove batch effects, enabling accurate downstream analysis
NormCap is a genomic data normalization tool developed by the Broad Institute. It helps remove technical noise and batch effects that can obscure true biological signals in genomic data sets.
When working with genomic data from different experiments, platforms, or batches, systematic non-biological differences can creep in and distort analyses like differential expression testing, clustering, and more. NormCap uses empirical Bayes-based adjustments to standardize mean and variability across features in your data set.
After normalization with NormCap, technical artifacts are minimized so you can uncover real biology. It works for common genomics assays like RNA-seq, ATAC-seq, proteomics, and others. By harmonizing data sets, NormCap enables integrated analysis of data from public repositories alongside your own internal data.
NormCap is freely available as an R/Bioconductor package. It allows you to easily normalize data compendia for more accurate downstream analyes like differential expresion testing, biomarker discovery, cell type mapping, and more.
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