High-throughput genome scaffolding from in vivo DNA interaction frequency
Program in Systems Biology; Department of Biochemistry and Molecular Pharmacology
Computational Biology | Systems Biology
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.
DOI of Published Version
Kaplan N, Dekker J. High-throughput genome scaffolding from in vivo DNA interaction frequency. Nat Biotechnol. 2013 Nov 24. doi: 10.1038/nbt.2768. Link to article on publisher's site
Kaplan N, Dekker J. (2013). High-throughput genome scaffolding from in vivo DNA interaction frequency. Program in Systems Biology Publications. https://doi.org/10.1038/nbt.2768. Retrieved from https://escholarship.umassmed.edu/sysbio_pubs/35