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key points for multi-sample analysis
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lgeistlinger committed May 19, 2024
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- TODO

- Batch effects are systematic technical differences in the observed expression
in cells measured in different experimental batches.
- Computational removal of batch-to-batch variation with the `correctExperiment`
function from the `r Biocpkg("batchelor")` package allows us to combine data
across multiple batches for a consolidated downstream analysis.
- Differential expression (DE) analysis of replicated multi-condition scRNA-seq experiments
is typically based on pseudo-bulk expression profiles, generated by summing
counts for all cells with the same combination of label and sample.
- The `aggregateAcrossCells` function from the `r Biocpkg("scater")` package
facilitates the creation of pseudo-bulk samples.
- The `pseudoBulkDGE` function from the `r Biocpkg("scran")` package can be used
to detect significant changes in expression between conditions for pseudo-bulk samples
consisting of cells of the same type.
- Differential abundance (DA) analysis aims at identifying significant changes in
cell type abundance across conditions.
- DA analysis uses bulk DE methods such as `r Biocpkg("edgeR")` and `r Biocpkg("DESeq2")`,
which provide suitable statistical models for count data in the presence of
limited replication - except that the counts are not of reads per gene, but
of cells per label.
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