| Literature DB >> 34183680 |
Vasanthan Jayakumar1, Osamu Nishimura2, Mitsutaka Kadota2, Naoki Hirose3,4,5, Hiromi Sano3,6, Yasuhiro Murakawa6,7,5,8,9, Yumiko Yamamoto10, Masataka Nakaya11,12, Tomoyuki Tsukiyama11,12, Yasunari Seita11, Shinichiro Nakamura11,12, Jun Kawai7, Erika Sasaki13, Masatsugu Ema11,12, Shigehiro Kuraku2, Hideya Kawaji14,15,16, Yasubumi Sakakibara17.
Abstract
Cynomolgus macaque (Macaca fascicularis) and common marmoset (Callithrix jacchus) have been widely used in human biomedical research. Long-standing primate genome assemblies used the human genome as a reference for ordering and orienting the assembled fragments into chromosomes. Here we performed de novo genome assembly of these two species without any human genome-based bias observed in the genome assemblies released earlier. We assembled PacBio long reads, and the resultant contigs were scaffolded with Hi-C data, which were further refined based on Hi-C contact maps and alternate de novo assemblies. The assemblies achieved scaffold N50 lengths of 149 Mb and 137 Mb for cynomolgus macaque and common marmoset, respectively. The high fidelity of our assembly is also ascertained by BAC-end concordance in common marmoset. Our assembly of cynomolgus macaque outperformed all the available assemblies of this species in terms of contiguity. The chromosome-scale genome assemblies produced in this study are valuable resources for non-human primate models and provide an important baseline in human biomedical research.Entities:
Year: 2021 PMID: 34183680 DOI: 10.1038/s41597-021-00935-6
Source DB: PubMed Journal: Sci Data ISSN: 2052-4463 Impact factor: 6.444