De Novo Genome and Transcriptome Assembly of the Canadian Beaver (Castor canadensis)

Author:

Lok Si12,Paton Tara A12,Wang Zhuozhi12,Kaur Gaganjot12,Walker Susan12,Yuen Ryan K C12,Sung Wilson W L12,Whitney Joseph12,Buchanan Janet A12,Trost Brett12,Singh Naina12,Apresto Beverly12,Chen Nan12,Coole Matthew12,Dawson Travis J12,Ho Karen12,Hu Zhizhou12,Pullenayegum Sanjeev12,Samler Kozue12,Shipstone Arun12,Tsoi Fiona12,Wang Ting12,Pereira Sergio L12,Rostami Pirooz12,Ryan Carol Ann12,Tong Amy Hin Yan3,Ng Karen4,Sundaravadanam Yogi4,Simpson Jared T45,Lim Burton K6,Engstrom Mark D6,Dutton Christopher J7,Kerr Kevin C R7,Franke Maria7,Rapley William7,Wintle Richard F12,Scherer Stephen W1289

Affiliation:

1. The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada

2. Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada

3. Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Ontario M5S 3E1, Canada

4. Ontario Institute for Cancer Research, MaRS Centre, Toronto, Ontario M5G 0A3, Canada

5. Department of Computer Science, University of Toronto, Ontario M5S 3G4, Canada

6. Department of Natural History, Royal Ontario Museum, Toronto, Ontario M5S 2C6, Canada

7. Toronto Zoo, Ontario M1B 5K7, Canada

8. McLaughlin Centre, University of Toronto, Ontario M5S 0A4, Canada

9. Department of Molecular Genetics, Faculty of Medicine, University of Toronto, Ontario M5S 1A8, Canada

Abstract

Abstract The Canadian beaver (Castor canadensis) is the largest indigenous rodent in North America. We report a draft annotated assembly of the beaver genome, the first for a large rodent and the first mammalian genome assembled directly from uncorrected and moderate coverage (< 30 ×) long reads generated by single-molecule sequencing. The genome size is 2.7 Gb estimated by k-mer analysis. We assembled the beaver genome using the new Canu assembler optimized for noisy reads. The resulting assembly was refined using Pilon supported by short reads (80 ×) and checked for accuracy by congruency against an independent short read assembly. We scaffolded the assembly using the exon–gene models derived from 9805 full-length open reading frames (FL-ORFs) constructed from the beaver leukocyte and muscle transcriptomes. The final assembly comprised 22,515 contigs with an N50 of 278,680 bp and an N50-scaffold of 317,558 bp. Maximum contig and scaffold lengths were 3.3 and 4.2 Mb, respectively, with a combined scaffold length representing 92% of the estimated genome size. The completeness and accuracy of the scaffold assembly was demonstrated by the precise exon placement for 91.1% of the 9805 assembled FL-ORFs and 83.1% of the BUSCO (Benchmarking Universal Single-Copy Orthologs) gene set used to assess the quality of genome assemblies. Well-represented were genes involved in dentition and enamel deposition, defining characteristics of rodents with which the beaver is well-endowed. The study provides insights for genome assembly and an important genomics resource for Castoridae and rodent evolutionary biology.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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