» Articles » PMID: 24270850

High-throughput Genome Scaffolding from in Vivo DNA Interaction Frequency

Overview
Journal Nat Biotechnol
Specialty Biotechnology
Date 2013 Nov 26
PMID 24270850
Citations 111
Authors
Affiliations
Soon will be listed here.
Abstract

Despite advances in DNA sequencing technology, assembly of complex genomes remains a major challenge, particularly for genomes sequenced using short reads, which yield highly fragmented assemblies. Here we show that genome-wide in vivo chromatin interaction frequency data, which are measurable with chromosome conformation capture-based experiments, can be used as genomic distance proxies to accurately position individual contigs without requiring any sequence overlap. We also use these data to construct approximate genome scaffolds de novo. Applying our approach to incomplete regions of the human genome, we predict the positions of 65 previously unplaced contigs, in agreement with alternative methods in 26/31 cases attempted in common. Our approach can theoretically bridge any gap size and should be applicable to any species for which global chromatin interaction data can be generated.

Citing Articles

Leveraging a phased pangenome for haplotype design of hybrid potato.

Cheng L, Wang N, Bao Z, Zhou Q, Guarracino A, Yang Y Nature. 2025; .

PMID: 39843749 DOI: 10.1038/s41586-024-08476-9.


Genome evolution and diversity of wild and cultivated rice species.

Long W, He Q, Wang Y, Wang Y, Wang J, Yuan Z Nat Commun. 2024; 15(1):9994.

PMID: 39557856 PMC: 11574199. DOI: 10.1038/s41467-024-54427-3.


The chromosome folding problem and how cells solve it.

Dekker J, Mirny L Cell. 2024; 187(23):6424-6450.

PMID: 39547207 PMC: 11569382. DOI: 10.1016/j.cell.2024.10.026.


Crosslinking intensity modulates the reliability and sensitivity of chromatin conformation detection at different structural levels.

Xu B, Gao X, Li X, Li F, Zhang Z Commun Biol. 2024; 7(1):1216.

PMID: 39349577 PMC: 11442689. DOI: 10.1038/s42003-024-06904-0.


A deep learning-based method enables the automatic and accurate assembly of chromosome-level genomes.

Jiang Z, Peng Z, Wei Z, Sun J, Luo Y, Bie L Nucleic Acids Res. 2024; 52(19):e92.

PMID: 39287126 PMC: 11514472. DOI: 10.1093/nar/gkae789.


References
1.
Birney E . Assemblies: the good, the bad, the ugly. Nat Methods. 2010; 8(1):59-60. DOI: 10.1038/nmeth0111-59. View

2.
Simonis M, Klous P, Splinter E, Moshkin Y, Willemsen R, de Wit E . Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C). Nat Genet. 2006; 38(11):1348-54. DOI: 10.1038/ng1896. View

3.
Yaffe E, Tanay A . Probabilistic modeling of Hi-C contact maps eliminates systematic biases to characterize global chromosomal architecture. Nat Genet. 2011; 43(11):1059-65. DOI: 10.1038/ng.947. View

4.
Dekker J, Marti-Renom M, Mirny L . Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data. Nat Rev Genet. 2013; 14(6):390-403. PMC: 3874835. DOI: 10.1038/nrg3454. View

5.
Cheung V, Nowak N, Jang W, Kirsch I, Zhao S, Chen X . Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature. 2001; 409(6822):953-8. PMC: 7845515. DOI: 10.1038/35057192. View