Researchers have assembled thousands of eukaryotic genomes using Illumina reads, but traditional mate-pair libraries cannot span all repetitive elements, resulting in highly fragmented assemblies. However, both chromosome conformation capture techniques, such as Hi-C and Dovetail Genomics Chicago libraries and long-read sequencing, such as Pacific Biosciences and Oxford Nanopore, help span and resolve repetitive regions and therefore improve genome assemblies. One important livestock species of arid regions that does not have a high-quality contiguous reference genome is the dromedary (Camelus dromedarius). Draft genomes exist but are highly fragmented, and a high-quality reference genome is needed to understand adaptation to desert environments and artificial selection during domestication. Dromedaries are among the last livestock species to have been domesticated, and together with wild and domestic Bactrian camels, they are the only representatives of the Camelini tribe, which highlights their evolutionary significance. Here we describe our efforts to improve the North African dromedary genome. We used Chicago and Hi-C sequencing libraries from Dovetail Genomics to resolve the order of previously assembled contigs, producing almost chromosome-level scaffolds. Remaining gaps were filled with Pacific Biosciences long reads, and then scaffolds were comparatively mapped to chromosomes. Long reads added 99.32 Mbp to the total length of the new assembly. Dovetail Chicago and Hi-C libraries increased the longest scaffold over 12-fold, from 9.71 Mbp to 124.99 Mbp and the scaffold N50 over 50-fold, from 1.48 Mbp to 75.02 Mbp. We demonstrate that Illumina de novo assemblies can be substantially upgraded by combining chromosome conformation capture and long-read sequencing.

Bristol Medical School Translational Health Sciences Molecular Neuroendocrinology Research Group University of Bristol Bristol UK

Department of Animal Genetics Faculty of Veterinary Medicine Ceitec VFU RG Animal Immunogenomics University of Veterinary and Pharmaceutical Sciences Brno Czech Republic

Department of Biostatistics University of Oslo Oslo Norway

Department of Integrative Biology and Evolution Research Institute of Wildlife Ecology Vetmeduni Vienna Vienna Austria

Department of Mathematics and Statistics University of Helsinki Helsinki Finland

Institute of Molecular and Cellular Biology SB RAS and Novosibirsk State University Novosibirsk Russia

Intelligent Systems Laboratory University of Bristol Bristol UK

The Walter Reed Biosystematics Unit Smithsonian Institution Museum Support Center MRC 534 Suitland Maryland

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Microsatellite markers of the major histocompatibility complex genomic region of domestic camels

Crimean-Congo Hemorrhagic Fever Virus Past Infections Are Associated with Two Innate Immune Response Candidate Genes in Dromedaries

Innate and Adaptive Immune Genes Associated with MERS-CoV Infection in Dromedaries

A Deadly Cargo: Gene Repertoire of Cytotoxic Effector Proteins in the Camelidae

Nucleotide diversity of functionally different groups of immune response genes in Old World camels based on newly annotated and reference-guided assemblies

The Major Histocompatibility Complex of Old World Camels-A Synopsis

Natural Killer Cell Receptor Genes in Camels: Another Mammalian Model

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GENBANK
GCA_000803125.1, GCA_000767585.1, GCA_000767855.1, GCA_000311805.2, GCA_000003055.3, SRP014573, GCF_000767855.1, GCF_000003055.6, GCF_000311805.1, GCF_000164845.2