An improved ovine reference genome assembly to facilitate in-depth functional annotation of the sheep genome

被引:26
作者
Davenport, Kimberly M. [1 ]
Bickhart, Derek M. [2 ]
Worley, Kim [3 ]
Murali, Shwetha C. [3 ]
Salavati, Mazdak [4 ]
Clark, Emily L. [4 ]
Cockett, Noelle E. [5 ]
Heaton, Michael P. [6 ]
Smith, Timothy P. L. [6 ]
Murdoch, Brenda M. [1 ]
Rosen, Benjamin D. [7 ]
机构
[1] Univ Idaho, Dept Anim Vet & Food Sci, 875 Perimeter Dr, Moscow, ID 83843 USA
[2] ARS, US Dairy Forage Res Ctr, USDA, 1925 Linden Dr, Madison, WI 53706 USA
[3] Baylor Coll Med, 1 Baylor Plaza, Houston, TX 77030 USA
[4] Univ Edinburgh, Roslin Inst, Royal Dick Sch Vet Studies, Easter Bush Campus, Roslin EH25 9RG, Midlothian, Scotland
[5] Utah State Univ, Old Main Hill, Logan, UT 84322 USA
[6] ARS, US Meat Anim Res Ctr, USDA, State Spur 18D, Clay Ctr, NE 68933 USA
[7] ARS, Anim Genom & Improvement Lab, USDA, 10300 Baltimore Ave, Beltsville, MD 20705 USA
来源
GIGASCIENCE | 2022年 / 11卷
基金
美国食品与农业研究所;
关键词
Rambouillet; genome assembly; reference genome; sheep; Ovis aries; ST-CROIX; DOMESTICATION; RESISTANCE; HISTORY;
D O I
10.1093/gigascience/giab096
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The domestic sheep (Ovis aries) is an important agricultural species raised for meat, wool, and milk across the world. A high-quality reference genome for this species enhances the ability to discover genetic mechanisms influencing biological traits. Furthermore, a high-quality reference genome allows for precise functional annotation of gene regulatory elements. The rapid advances in genome assembly algorithms and emergence of sequencing technologies with increasingly long reads provide the opportunity for an improved de novo assembly of the sheep reference genome. Findings Short-read Illumina (55x coverage), long-read Pacific Biosciences (75x coverage), and Hi-C data from this ewe retrieved from public databases were combined with an additional 50x coverage of Oxford Nanopore data and assembled with canu v1.9. The assembled contigs were scaffolded using Hi-C data with Salsa v2.2, gaps filled with PBsuitev15.8.24, and polished with Nanopolish v0.12.5. After duplicate contig removal with PurgeDups v1.0.1, chromosomes were oriented and polished with 2 rounds of a pipeline that consisted of freebayes v1.3.1 to call variants, Merfin to validate them, and BCFtools to generate the consensus fasta. The ARS-UI_Ramb_v2.0 assembly is 2.63 Gb in length and has improved continuity (contig NG50 of 43.18 Mb), with a 19- and 38-fold decrease in the number of scaffolds compared with Oar_rambouillet_v1.0 and Oar_v4.0. ARS-UI_Ramb_v2.0 has greater per-base accuracy and fewer insertions and deletions identified from mapped RNA sequence than previous assemblies. Conclusions The ARS-UI_Ramb_v2.0 assembly is a substantial improvement in contiguity that will optimize the functional annotation of the sheep genome and facilitate improved mapping accuracy of genetic variant and expression data for traits in sheep.
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页数:9
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