Puzzle Hi-C: an accurate scaffolding software
Guoliang LiniD, Zhiru Huang, Tingsong Yue, Jing ChaiiD, Yan LiiD, Huimin YangiD, Wanting Qin, Guobing YangiD, Robert W. MurphyiD, Ya‐Ping ZhangiD, Zijie Scott ZhangiD, Wei Hu ZhouiD, Jing LuoiD
Abstract
High-quality, chromosome-scale genomes are essential for genomic analyses. Analyses, including 3D genomics, epigenetics, and comparative genomics rely on a high-quality genome assembly, which is often accomplished with the assistance of Hi-C data. Current Hi-C-assisted assembling algorithms either generate ordering and orientation errors or fail to assemble high-quality chromosome-level scaffolds. Here, we offer the software Puzzle Hi-C, which uses Hi-C reads to accurately assign contigs or scaffolds to chromosomes. Puzzle Hi-C uses the triangle region instead of the square region to count interactions in a Hi-C heatmap. This strategy dramatically diminishes scaffolding interference caused by long-range interactions. This software also introduces a dynamic, triangle window strategy during assembly. Initially small, the window expands with interactions to produce more effective clustering. Puzzle Hi-C outperforms available scaffolding tools.
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