染色质
计算生物学
转录组
生物
DNA
芯片排序
基因
遗传学
基因表达
染色质重塑
作者
Chenxu Zhu,Zhaoning Wang,Bing Ren
标识
DOI:10.1007/978-1-0716-2899-7_10
摘要
Simultaneous detection of chromatin accessibility and transcription from the same cells promises to greatly facilitate the dissection of cell-type-specific gene regulatory programs in complex tissues. Paired-seq enables joint analysis of open chromatin and nuclear transcriptome from up to a million cells in parallel. It achieves ultra-high-throughput single-cell multiomics with the use of a combinatorial barcoding strategy involving sequential ligation of multiplexed DNA barcodes to chromatin DNA fragments and reverse transcription products, followed by high-throughput DNA sequencing of the resulting DNA libraries and deconvolution of single-cell multiomic maps based on cell-specific barcodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI