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中国恒河猴的基因组序列和全球序列变异图谱,包含 550 万个单核苷酸多态性(SNP)。

Genome sequence and global sequence variation map with 5.5 million SNPs in Chinese rhesus macaque.

机构信息

Beijing Genomics Institute-Shenzhen, Chinese Academy of Sciences, Shenzhen 518083, China.

出版信息

Genome Biol. 2011 Jul 6;12(7):R63. doi: 10.1186/gb-2011-12-7-r63.

Abstract

BACKGROUND

Rhesus macaque (Macaca mulatta) is the most widely used nonhuman primate animal in biomedical research. A global map of genetic variations in rhesus macaque is valuable for both evolutionary and functional studies.

RESULTS

Using next-generation sequencing technology, we sequenced a Chinese rhesus macaque genome with 11.56-fold coverage. In total, 96% of the reference Indian macaque genome was covered by at least one read, and we identified 2.56 million homozygous and 2.94 million heterozygous SNPs. We also detected a total of 125,150 structural variations, of which 123,610 were deletions with a median length of 184 bp (ranging from 25 bp to 10 kb); 63% of these deletions were located in intergenic regions and 35% in intronic regions. We further annotated 5,187 and 962 nonsynonymous SNPs to the macaque orthologs of human disease and drug-target genes, respectively. Finally, we set up a genome-wide genetic variation database with the use of Gbrowse.

CONCLUSIONS

Genome sequencing and construction of a global sequence variation map in Chinese rhesus macaque with the concomitant database provide applicable resources for evolutionary and biomedical research.

摘要

背景

恒河猴(Macaca mulatta)是生物医学研究中应用最广泛的非人类灵长类动物。恒河猴遗传变异的全球图谱对于进化和功能研究都具有重要价值。

结果

我们使用新一代测序技术对一只中国恒河猴进行了测序,测序深度为 11.56 倍。总的来说,至少有一个读取覆盖了参考印度恒河猴基因组的 96%,我们鉴定出了 256 万个纯合子和 2940 万个杂合子 SNP。我们还总共检测到 125150 个结构变异,其中 123610 个是缺失,中位数长度为 184bp(范围从 25bp 到 10kb);这些缺失中有 63%位于基因间区,35%位于内含子区。我们进一步注释了 5187 个和 962 个非同义 SNP 到恒河猴与人疾病和药物靶点基因的同源基因。最后,我们使用 Gbrowse 建立了一个全基因组遗传变异数据库。

结论

中国恒河猴的基因组测序和全球序列变异图谱的构建及其数据库的建立为进化和生物医学研究提供了可用资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ba5/3218825/6fef91e7721e/gb-2011-12-7-r63-1.jpg

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