A 3-way hybrid approach to generate a new high-quality chimpanzee reference genome (Pan_tro_3.0)
Author(s) -
Lukas F. K. Kuderna,
Chad Tomlinson,
LaDeana Hillier,
Annabel Tran,
Ian T. Fiddes,
Joel Armstrong,
Hafid Laayouni,
David Gordon,
John Huddleston,
Raquel García-Pérez,
Inna Povolotskaya,
Aitor Serres Armero,
Jèssica GómezGarrido,
Daniel Ho,
Paolo Ribeca,
Tyler Alioto,
Richard E. Green,
Benedict Paten,
Arcadi Navarro,
Jaume Betranpetit,
Javier Herrero,
Evan E. Eichler,
Andrew J. Sharp,
Lars Feuk,
Wesley C. Warren,
Tomás MarquèsBonet
Publication year - 2017
Publication title -
gigascience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.947
H-Index - 54
ISSN - 2047-217X
DOI - 10.1093/gigascience/gix098
Subject(s) - contig , reference genome , genome , sequence assembly , genome project , computational biology , biology , hybrid genome assembly , contiguity , human genome , genetics , gene , transcriptome , ecology , gene expression
The chimpanzee is arguably the most important species for the study of human origins. A key resource for these studies is a high-quality reference genome assembly; however, as with most mammalian genomes, the current iteration of the chimpanzee reference genome assembly is highly fragmented. In the current iteration of the chimpanzee reference genome assembly (Pan_tro_2.1.4), the sequence is scattered across more then 183 000 contigs, incorporating more than 159 000 gaps, with a genome-wide contig N50 of 51 Kbp. In this work, we produce an extensive and diverse array of sequencing datasets to rapidly assemble a new chimpanzee reference that surpasses previous iterations in bases represented and organized in large scaffolds. To this end, we show substantial improvements over the current release of the chimpanzee genome (Pan_tro_2.1.4) by several metrics, such as increased contiguity by >750% and 300% on contigs and scaffolds, respectively, and closure of 77% of gaps in the Pan_tro_2.1.4 assembly gaps spanning >850 Kbp of the novel coding sequence based on RNASeq data. We further report more than 2700 genes that had putatively erroneous frame-shift predictions to human in Pan_tro_2.1.4 and show a substantial increase in the annotation of repetitive elements. We apply a simple 3-way hybrid approach to considerably improve the reference genome assembly for the chimpanzee, providing a valuable resource for the study of human origins. Furthermore, we produce extensive sequencing datasets that are all derived from the same cell line, generating a broad non-human benchmark dataset.
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