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Direct transposition of native DNA for sensitive multimodal single-molecule sequencing I

ABSTRACT: Direct transposition of native DNA for sensitive multimodal single-molecule sequencing I

PROVIDER: PRJNA864052 | ENA |

REPOSITORIES: ENA

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Dataset's files

Source:

			Action	DRS
	SRR20724684_subreads.fastq.gz	Fastqsanger.gz
	SRR20724685_subreads.fastq.gz	Fastqsanger.gz
	SRR20724686_subreads.fastq.gz	Fastqsanger.gz
	SRR20724687_subreads.fastq.gz	Fastqsanger.gz
	SRR20724688_subreads.fastq.gz	Fastqsanger.gz

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Project description:Concurrent readout of sequence and base modifications from long unamplified DNA templates by PacBio single-molecule sequencing requires large amounts of input material. Here we adapt Tn5 transposition to introduce hairpin oligonucleotides and fragment (tagment) limiting quantities of DNA for generating PacBio-compatible circular molecules. We developed two methods that implement tagmentation and use 90–99% less input than current protocols: (1) single-molecule real-time sequencing by tagmentation (SMRT-Tag), which allows detection of genetic variation and CpG methylation; and (2) single-molecule adenine-methylated oligonucleosome sequencing assay by tagmentation (SAMOSA-Tag), which uses exogenous adenine methylation to add a third channel for probing chromatin accessibility. SMRT-Tag of 40 ng or more human DNA (approximately 7,000 cell equivalents) yielded data comparable to gold standard whole-genome and bisulfite sequencing. SAMOSA-Tag of 30,000–50,000 nuclei resolved single-fiber chromatin structure, CTCF binding and DNA methylation in patient-derived prostate cancer xenografts and uncovered metastasis-associated global epigenome disorganization. Tagmentation thus promises to enable sensitive, scalable and multimodal single-molecule genomics for diverse basic and clinical applications.

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