ArticleG3 (Bethesda, Md.)2023
Chromosomal-level reference genome of a wild North American mallard (Anas platyrhynchos).
Article in G3 (Bethesda, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Assessing consequences of anthropogenic hybridization: Great Lakes mallard movement and resource selection.Movement ecology · 2026Article
- Unknown Biases: Understanding How Anthropogenic Hybridization Impacts Genomic Diversity and Demographic Estimates.Animals : an open access journal from MDPI · 2026Article
- Whole genome sequence analysis supports the genomic mosaicism of the endangered Hawaiian duck (Anas wyvilliana).Scientific reports · 2026Article
- Anthropogenic Hybridization Contributes to the Naturalization of Introduced Domestic Mallards (Ecology and evolution · 2025Article
- A high-quality assembly revealing the PMEL gene for the unique plumage phenotype in Liancheng ducks.GigaScience · 2025Article
- Human-Induced Range Expansions Result in a Recent Hybrid Zone between Sister Species of Ducks.Genes · 2024Article
- Consistent changes in muscle metabolism underlie dive performance across multiple lineages of diving ducks.Proceedings. Biological sciences · 2023Article
- The meaning of wild: Genetic and adaptive consequences from large-scale releases of domestic mallards.Communications biology · 2023Article
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Authors and funding
4 authors.
Funding
Abstract
The mallard (Anas platyrhynchos) is one of the most common, economically, and socially important birds around the world. Mallards were not only an important food source for early humans but eventually becoming intimately linked with people as they were domesticated over the last 2,000 years. To date, mallard genomes are largely reconstructed from samples of domestic or unknown genetic heritage. Here, we report the first high-quality genome assembly and annotation of a genetically vetted wild mallard from North America (NAwild_v1.0). The genome was assembled using a combination of shotgun libraries, proximity ligation Chicago, and Dovetail Hi-C libraries. The final assembly is ∼1.04 Gb in size, with 98.3% of the sequence located in 30 full or nearly full chromosome-level scaffolds, and with a N50/L50 of 79.1 Mb/4 scaffolds. We used a combination of gene prediction and similarity approaches to annotate a total of 23,584 functional genes, of which 19,242 were associated to GO terms. The genome assembly and the set of annotated genes yielded a 95.4% completeness score when compared with the BUSCO aves_odb10 dataset. Next, we aligned 3 previously published mallard genomes to ours, and demonstrate how runs of homozygosity and nucleotide diversity are substantially higher and lower, respectively, to ours and how these artificially changed genomes resulted in profoundly different and biased demographic histories. Our wild mallard assembly not only provides a valuable resource to shed light onto genome evolution, speciation, and other adaptive processes, but also helping with identifying functional genes that have been significantly altered during the domestication process.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.