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引用次数: 0
摘要
我们展示了红冠雉(Netta rufina;脊索动物门;鸟纲;雉形目;雉科)雌性标本的基因组序列。基因组序列总长度为 1,167.00 兆字节。基因组的大部分(98.76%)组装成 42 个染色体假分子支架,包括 Z 和 W 性染色体。线粒体基因组也已组装完成,长度为 16.62 千碱基。
The genome sequence of the red-crested pochard, Netta rufina (Pallas, 1773).
We present a genome assembly from a female specimen of Netta rufina (the red-crested pochard; Chordata; Aves; Anseriformes; Anatidae). The genome sequence has a total length of 1,167.00 megabases. Most of the assembly (98.76%) is scaffolded into 42 chromosomal pseudomolecules, including the Z and W sex chromosomes. The mitochondrial genome has also been assembled and is 16.62 kilobases in length.
Wellcome Open ResearchBiochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
5.50
自引率
0.00%
发文量
426
审稿时长
1 weeks
期刊介绍:
Wellcome Open Research publishes scholarly articles reporting any basic scientific, translational and clinical research that has been funded (or co-funded) by Wellcome. Each publication must have at least one author who has been, or still is, a recipient of a Wellcome grant. Articles must be original (not duplications). All research, including clinical trials, systematic reviews, software tools, method articles, and many others, is welcome and will be published irrespective of the perceived level of interest or novelty; confirmatory and negative results, as well as null studies are all suitable. See the full list of article types here. All articles are published using a fully transparent, author-driven model: the authors are solely responsible for the content of their article. Invited peer review takes place openly after publication, and the authors play a crucial role in ensuring that the article is peer-reviewed by independent experts in a timely manner. Articles that pass peer review will be indexed in PubMed and elsewhere. Wellcome Open Research is an Open Research platform: all articles are published open access; the publishing and peer-review processes are fully transparent; and authors are asked to include detailed descriptions of methods and to provide full and easy access to source data underlying the results to improve reproducibility.