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

2011 ◽  
Vol 12 (7) ◽  
Author(s):  
Xiaodong Fang ◽  
Yanfeng Zhang ◽  
Rui Zhang ◽  
Lixin Yang ◽  
Ming Li ◽  
...  
2004 ◽  
Vol 49 (17) ◽  
pp. 1824-1827 ◽  
Author(s):  
Weiwu Jin ◽  
Liangxiang Hu ◽  
Zhenglin Du ◽  
Qiang Gao ◽  
Hong Gao ◽  
...  

2020 ◽  
Author(s):  
Pablo Baeza-Centurion ◽  
Belén Miñana ◽  
Juan Valcárcel ◽  
Ben Lehner

AbstractGenetic analyses and systematic mutagenesis have revealed that synonymous, non-synonymous and intronic mutations frequently alter the inclusion levels of alternatively spliced exons, consistent with the concept that altered splicing might be a common mechanism by which mutations cause disease. However, most exons expressed in any cell are highly-included in mature mRNAs. Here, by performing deep mutagenesis of highly-included exons and by analysing the association between genome sequence variation and exon inclusion across the transcriptome, we report that mutations only very rarely alter the inclusion of highly-included exons. This is true for both exonic and intronic mutations as well as for perturbations in trans. Therefore, mutations that affect splicing are not evenly distributed across primary transcripts but are focussed in and around alternatively spliced exons with intermediate inclusion levels. These results provide a resource for prioritising synonymous and other variants as disease-causing mutations.


PLoS ONE ◽  
2019 ◽  
Vol 14 (9) ◽  
pp. e0222338 ◽  
Author(s):  
Wenhai Yu ◽  
Xianhui Hao ◽  
Fengmei Yang ◽  
Jin Ma ◽  
Yuan Zhao ◽  
...  

2008 ◽  
Vol 69 ◽  
pp. S45
Author(s):  
Jin Wu ◽  
Susan Bassinger ◽  
Bridget Holder-Locker ◽  
Carrie E. Jones ◽  
Leonard Chavez ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Yaoxi He ◽  
Xin Luo ◽  
Bin Zhou ◽  
Ting Hu ◽  
Xiaoyu Meng ◽  
...  

Abstract We present a high-quality de novo genome assembly (rheMacS) of the Chinese rhesus macaque (Macaca mulatta) using long-read sequencing and multiplatform scaffolding approaches. Compared to the current Indian rhesus macaque reference genome (rheMac8), rheMacS increases sequence contiguity 75-fold, closing 21,940 of the remaining assembly gaps (60.8 Mbp). We improve gene annotation by generating more than two million full-length transcripts from ten different tissues by long-read RNA sequencing. We sequence resolve 53,916 structural variants (96% novel) and identify 17,000 ape-specific structural variants (ASSVs) based on comparison to ape genomes. Many ASSVs map within ChIP-seq predicted enhancer regions where apes and macaque show diverged enhancer activity and gene expression. We further characterize a subset that may contribute to ape- or great-ape-specific phenotypic traits, including taillessness, brain volume expansion, improved manual dexterity, and large body size. The rheMacS genome assembly serves as an ideal reference for future biomedical and evolutionary studies.


2011 ◽  
Vol 63 (5) ◽  
pp. 275-290 ◽  
Author(s):  
Scott Southwood ◽  
Christopher Solomon ◽  
Ilka Hoof ◽  
Richard Rudersdorf ◽  
John Sidney ◽  
...  

2013 ◽  
Vol 33 (1) ◽  
pp. 49-54
Author(s):  
Lin ZHU ◽  
Jian-Bao HAN ◽  
Xi-He ZHANG ◽  
Jian-Ping MA ◽  
Long-Bao LÜ ◽  
...  

2017 ◽  
Vol 5 (33) ◽  
Author(s):  
Subhiksha Nandakumar ◽  
Eunhae H. Bae ◽  
Arifa S. Khan

ABSTRACT The full-length genome sequence of a simian foamy virus (SFVmmu_K3T), isolated from a rhesus macaque (Macaca mulatta), was obtained using high-throughput sequencing. SFVmmu_K3T consisted of 12,983 bp and had a genomic organization similar to that of other SFVs, with long terminal repeats (LTRs) and open reading frames for Gag, Pol, Env, Tas, and Bet.


PLoS ONE ◽  
2013 ◽  
Vol 8 (2) ◽  
pp. e55315 ◽  
Author(s):  
Shan-Jin Wu ◽  
Jing Luo ◽  
Qing-Qing Li ◽  
Yan-Qin Wang ◽  
Robert W. Murphy ◽  
...  

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