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作 者:Lei Chen Long Jin Mingzhou Li Shilin Tian Tiandong Che Qianzi Tang Jing Lan Zhi Jiang Ruiqiang Li Yiren Gu Xuewei Li Jinyong Wang
机构地区:[1]Chongqing Academy of Animal Sciences [2]Key Laboratory of Pig Industry Sciences, Ministry of Agriculture [3]Institute of Animal Genetics and Breeding,college of Animal Science and Technology, Sichuan Agricultural University [4]Novogene Bioinjormatics Institute [5]Sichuan Ammal Science Academy
出 处:《Journal of Genetics and Genomics》2014年第12期653-657,共5页遗传学报(英文版)
基 金:supported by the National High Technology Research and Development Program of China(863 Program)(No.2013AA102502);the National Natural Science Foundation of China(Nos.31372284 and 31402046);the Fund of Fok Ying-Tung Education Foundation(No.141117);the Fund for Distinguished Young Scientists of Sichuan Province(No. 2013JQ0013)
摘 要:Genomic structural variations (SVs), particularly insertions, deletions and inversions, can contribute to the heterogeneity of millions of nucleotides within a genome, and are likely to make an important contribution to biological diversity and phenotypic variation (Alkan et al., 2011; Bickhart and Liu, 2014). With the rapid development of the next-generation sequencing technologies and the new assembly methodolo- gies, the multiple de novo assemblies of genomes within a species allow researchers to explore more detailed SV maps (Li et al., 2011). Compared with the traditional read depth algorithm using the whole-genome resequencing approach and array-based technologies (Baker, 2012; Wang et al., 2012;Genomic structural variations (SVs), particularly insertions, deletions and inversions, can contribute to the heterogeneity of millions of nucleotides within a genome, and are likely to make an important contribution to biological diversity and phenotypic variation (Alkan et al., 2011; Bickhart and Liu, 2014). With the rapid development of the next-generation sequencing technologies and the new assembly methodolo- gies, the multiple de novo assemblies of genomes within a species allow researchers to explore more detailed SV maps (Li et al., 2011). Compared with the traditional read depth algorithm using the whole-genome resequencing approach and array-based technologies (Baker, 2012; Wang et al., 2012;
关 键 词:gene Snapshot of Structural Variations in the Tibetan Wild Boar Genome at Single-Nucleotide Resolution
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