cKBET: assessing goodness of batch effect correction for single-cell RNA-seq
Por um escritor misterioso
Last updated 22 fevereiro 2025
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lt;p>Single-cell RNA sequencing reveals the gene structure and gene expression status of a single cell, which can reflect the heterogeneity between cells. However, batch effects caused by non-biological factors may hinder data integration and downstream analysis. Although the batch effect can be evaluated by visualizing the data, which actually is subjective and inaccurate. In this work, we propose a quantitative method cKBET, which considers the batch and cell type information simultaneously. The cKBET method accesses batch effects by comparing the global and local fraction of cells of different batches in different cell types. We verify the performance of our cKBET method on simulated and real biological data sets. The experimental results show that our cKBET method is superior to existing methods in most cases. In general, our cKBET method can detect batch effect with either balanced or unbalanced cell types, and thus evaluate batch correction methods.</p>
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Assessment of batch-correction methods for scRNA-seq data with a new test metric
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cKBET: assessing goodness of batch effect correction for single-cell RNA-seq
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A benchmark of batch-effect correction methods for single-cell RNA sequencing data, Genome Biology
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cKBET: assessing goodness of batch effect correction for single-cell RNA-seq
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PDF] Projected t-SNE for batch correction
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A benchmark of batch-effect correction methods for single-cell RNA sequencing data, Genome Biology
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12 Batch Correction Lab ANALYSIS OF SINGLE CELL RNA-SEQ DATA
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CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq data
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PDF) BERMUDA: A novel deep transfer learning method for single-cell RNA sequencing batch correction reveals hidden high-resolution cellular subtypes
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Batch effects and the effective design of single-cell gene expression studies
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Fast, sensitive and accurate integration of single-cell data with Harmony
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CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq data
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