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CiFi:低输入量要求下的准确长读长染色质构象捕获。

CiFi: Accurate long-read chromatin conformation capture with low-input requirements.

作者信息

McGinty Sean P, Kaya Gulhan, Sim Sheina B, Corpuz Renée L, Quail Michael A, Lawniczak Mara K N, Geib Scott M, Korlach Jonas, Dennis Megan Y

机构信息

Genome Center, MIND Institute, and Department of Biochemistry & Molecular Medicine, University of California, Davis, CA 95616, USA.

U.S. Department of Agriculture, Agricultural Research Service, U.S. Pacific Basin Agricultural Research Center, Tropical Pest Genetics and Molecular Biology Research Unit, Hilo, HI 96720, USA.

出版信息

bioRxiv. 2025 Feb 5:2025.01.31.635566. doi: 10.1101/2025.01.31.635566.

DOI:10.1101/2025.01.31.635566
PMID:39975366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11838532/
Abstract

By coupling chromatin conformation capture (3C) with PacBio HiFi long-read sequencing, we have developed a new method (CiFi) that enables analysis of genome interactions across repetitive genomic regions with low-input requirements. CiFi produces multiple interacting concatemer segments per read, facilitating genome assembly and scaffolding. Together, the approach enables genomic analysis of previously recalcitrant low-complexity loci, and of small organisms such as single insect individuals.

摘要

通过将染色质构象捕获技术(3C)与PacBio HiFi长读长测序相结合,我们开发了一种新方法(CiFi),该方法能够在低输入要求下分析重复基因组区域的基因组相互作用。CiFi每个读段产生多个相互作用的串联体片段,有助于基因组组装和支架构建。总之,该方法能够对以前难以处理的低复杂性位点以及单个昆虫个体等小型生物体进行基因组分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/25539cba0079/nihpp-2025.01.31.635566v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/784780383718/nihpp-2025.01.31.635566v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/2c342e237d38/nihpp-2025.01.31.635566v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/25539cba0079/nihpp-2025.01.31.635566v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/784780383718/nihpp-2025.01.31.635566v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/2c342e237d38/nihpp-2025.01.31.635566v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/719d/11838532/25539cba0079/nihpp-2025.01.31.635566v1-f0003.jpg

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本文引用的文献

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SVbyEye: A visual tool to characterize structural variation among whole-genome assemblies.SVbyEye:一种用于表征全基因组组装之间结构变异的可视化工具。
Bioinformatics. 2025 Jun 6. doi: 10.1093/bioinformatics/btaf332.
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Long-read sequencing and genome assembly of natural history collection samples and challenging specimens.自然历史馆藏样本及具有挑战性的标本的长读长测序与基因组组装。
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Pairtools: From sequencing data to chromosome contacts.Pairtools:从测序数据到染色体接触。
PLoS Comput Biol. 2024 May 29;20(5):e1012164. doi: 10.1371/journal.pcbi.1012164. eCollection 2024 May.
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Scalable telomere-to-telomere assembly for diploid and polyploid genomes with double graph.使用双图进行二倍体和多倍体基因组的可扩展端粒到端粒组装。
Nat Methods. 2024 Jun;21(6):967-970. doi: 10.1038/s41592-024-02269-8. Epub 2024 May 10.
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Genome assembly in the telomere-to-telomere era.端粒到端粒时代的基因组组装。
Nat Rev Genet. 2024 Sep;25(9):658-670. doi: 10.1038/s41576-024-00718-w. Epub 2024 Apr 22.
6
Mitotic chromosomes are self-entangled and disentangle through a topoisomerase-II-dependent two-stage exit from mitosis.有丝分裂染色体通过拓扑异构酶 II 依赖性的两步过程从有丝分裂中自行缠绕和解缠绕。
Mol Cell. 2024 Apr 18;84(8):1422-1441.e14. doi: 10.1016/j.molcel.2024.02.025. Epub 2024 Mar 22.
7
Determining chromatin architecture with Micro Capture-C.运用 Micro Capture-C 技术确定染色质结构。
Nat Protoc. 2023 Jun;18(6):1687-1711. doi: 10.1038/s41596-023-00817-8. Epub 2023 Mar 29.
8
High-throughput Pore-C reveals the single-allele topology and cell type-specificity of 3D genome folding.高通量孔道技术揭示了三维基因组折叠的单等位基因拓扑结构和细胞类型特异性。
Nat Commun. 2023 Mar 6;14(1):1250. doi: 10.1038/s41467-023-36899-x.
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YaHS: yet another Hi-C scaffolding tool.YaHS:另一个 Hi-C 支架工具。
Bioinformatics. 2023 Jan 1;39(1). doi: 10.1093/bioinformatics/btac808.
10
Identifying synergistic high-order 3D chromatin conformations from genome-scale nanopore concatemer sequencing.从基因组规模的纳米孔串联测序中识别协同的高阶 3D 染色质构象。
Nat Biotechnol. 2022 Oct;40(10):1488-1499. doi: 10.1038/s41587-022-01289-z. Epub 2022 May 30.