Protocol for assay of transposase accessible chromatin sequencing in non-model species

The assay for transposase accessible chromatin (ATAC-seq) is a method for mapping genome-wide chromatin accessibility. Coupled with high-throughput sequencing, it enables integrative epigenomics analyses. ATAC-seq requires direct access to cell nuclei, a major challenge in non-model species such as...

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Veröffentlicht in:STAR protocols 2021-03, Vol.2 (1), p.100341-100341, Article 100341
Hauptverfasser: Kissane, Stephen, Dhandapani, Vignesh, Orsini, Luisa
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Sprache:eng
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Zusammenfassung:The assay for transposase accessible chromatin (ATAC-seq) is a method for mapping genome-wide chromatin accessibility. Coupled with high-throughput sequencing, it enables integrative epigenomics analyses. ATAC-seq requires direct access to cell nuclei, a major challenge in non-model species such as small invertebrates, whose soft tissue is surrounded by a protective exoskeleton. Here, we present modifications of the ATAC-seq protocol for applications in small crustaceans, extending applications to non-model species. For complete information on the use and execution of this protocol, please refer to Buenrostro et al. (2013). [Display omitted] •ATAC-seq modified protocol for applications in non-model species•Transposase titration identifies thresholds for optimal transposition at lower costs•Minimal number of cells/tissue is identified for low input reactions•Proof of concept ATAC-seq analysis for the waterflea Daphnia magna The assay for transposase accessible chromatin (ATAC-seq) is a method for mapping genome-wide chromatin accessibility. Coupled with high-throughput sequencing, it enables integrative epigenomics analyses. ATAC-seq requires direct access to cell nuclei, a major challenge in non-model species such as small invertebrates, whose soft tissue is surrounded by a protective exoskeleton. Here, we present modifications of the ATAC-seq protocol for applications in small crustaceans, extending applications to non-model species.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2021.100341