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一种长读测序策略,使用相邻片段上的重叠接头(OLAF-Seq)进行靶向重测序和富集。

A long-read sequencing strategy with overlapping linkers on adjacent fragments (OLAF-Seq) for targeted resequencing and enrichment.

机构信息

School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, 19104, USA.

Cancer Genome and Epigenetics Program, NCI-Designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, 92037, USA.

出版信息

Sci Rep. 2024 Mar 7;14(1):5583. doi: 10.1038/s41598-024-56402-w.

Abstract

In this report, we present OLAF-Seq, a novel strategy to construct a long-read sequencing library such that adjacent fragments are linked with end-terminal duplications. We use the CRISPR-Cas9 nickase enzyme and a pool of multiple sgRNAs to perform non-random fragmentation of targeted long DNA molecules (> 300kb) into smaller library-sized fragments (about 20 kbp) in a manner so as to retain physical linkage information (up to 1000 bp) between adjacent fragments. DNA molecules targeted for fragmentation are preferentially ligated with adaptors for sequencing, so this method can enrich targeted regions while taking advantage of the long-read sequencing platforms. This enables the sequencing of target regions with significantly lower total coverage, and the genome sequence within linker regions provides information for assembly and phasing. We demonstrated the validity and efficacy of the method first using phage and then by sequencing a panel of 100 full-length cancer-related genes (including both exons and introns) in the human genome. When the designed linkers contained heterozygous genetic variants, long haplotypes could be established. This sequencing strategy can be readily applied in both PacBio and Oxford Nanopore platforms for both long and short genes with an easy protocol. This economically viable approach is useful for targeted enrichment of hundreds of target genomic regions and where long no-gap contigs need deep sequencing.

摘要

在本报告中,我们提出了 OLAF-Seq 策略,用于构建长读测序文库,使相邻片段通过末端重复序列连接。我们使用 CRISPR-Cas9 核酸酶和多个 sgRNA 池对靶向长 DNA 分子(>300kb)进行非随机片段化,将其分割成更小的文库大小片段(约 20kbp),同时保留相邻片段之间的物理连接信息(最多 1000bp)。用于片段化的 DNA 分子优先与测序接头连接,因此该方法可以在利用长读测序平台的同时富集靶向区域。这使得靶向区域的测序总覆盖率显著降低,而连接区域内的基因组序列为组装和定相提供了信息。我们首先使用噬菌体验证了该方法的有效性和功效,然后对人类基因组中 100 个全长癌症相关基因(包括外显子和内含子)进行了测序。当设计的接头包含杂合遗传变异时,可以建立长单倍型。该测序策略可在 PacBio 和 Oxford Nanopore 平台上轻松应用于长基因和短基因,具有简单的方案。这种经济可行的方法可用于靶向富集数百个目标基因组区域,以及需要深度测序的长无间隙连续序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/072a/10917763/51167ace3fdb/41598_2024_56402_Fig1_HTML.jpg

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