Extended haplotype phasing of de novo genome assemblies with FALCON-Phase
Zev N. KronenbergiD, Arang RhieiD, Sergey KoreniD, Gregory T. ConcepcioniD, Paul S. PelusoiD, Katherine M. MunsoniD, David PorubskỳiD, Kristen L. KuhniD, Kathryn A. Mueller, Wai Yee LowiD, Stefan HiendlederiD, Olivier D. FedrigoiD, Ivan LiachkoiD, Richard J. HalliD, Adam M. PhillippyiD, Evan E. EichleriD, John Lewis WilliamsiD, Timothy P. L. SmithiD, Erich David JarvisiD, Shawn T SullivaniD, Sarah B. KinganiD
Abstract
Haplotype-resolved genome assemblies are important for understanding how combinations of variants impact phenotypes. These assemblies can be created in various ways, such as use of tissues that contain single-haplotype (haploid) genomes, or by co-sequencing of parental genomes, but these approaches can be impractical in many situations. We present FALCON-Phase, which integrates long-read sequencing data and ultra-long-range Hi-C chromatin interaction data of a diploid individual to create high-quality, phased diploid genome assemblies. The method was evaluated by application to three datasets, including human, cattle, and zebra finch, for which high-quality, fully haplotype resolved assemblies were available for benchmarking. Phasing algorithm accuracy was affected by heterozygosity of the individual sequenced, with higher accuracy for cattle and zebra finch (>97%) compared to human (82%). In addition, scaffolding with the same Hi-C chromatin contact data resulted in phased chromosome-scale scaffolds.
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