Integration of scATAC-Seq with scRNA-Seq Data

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Single Cell Transcriptomics

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2584))

Abstract

Single-cell studies are enabling our understanding of the molecular processes of normal cell development and the onset of several pathologies. For instance, single-cell RNA sequencing (scRNA-Seq) measures the transcriptome-wide gene expression at a single-cell resolution, allowing for studying the heterogeneity among the cells of the same population and revealing complex and rare cell populations. On the other hand, single-cell Assay for Transposase-Accessible Chromatin using sequencing (scATAC-Seq) can be used to define transcriptional and epigenetic changes by analyzing the chromatin accessibility at the single-cell level. However, the integration of multi-omics data still remains one of the most difficult tasks in bioinformatics. In this chapter, we focus on the combination of scRNA-Seq and scATACSeq data to perform an integrative analysis of the single-cell transcriptome and chromatin accessibility of human fetal progenitors.

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Correspondence to Andrea Tangherloni .

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Berest, I., Tangherloni, A. (2023). Integration of scATAC-Seq with scRNA-Seq Data. In: Calogero, R.A., Benes, V. (eds) Single Cell Transcriptomics. Methods in Molecular Biology, vol 2584. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2756-3_15

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  • DOI: https://doi.org/10.1007/978-1-0716-2756-3_15

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-2755-6

  • Online ISBN: 978-1-0716-2756-3

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