Reconstructing DNA copy number by joint segmentation of multiple sequences

被引：0
作者：
Zhongyang Zhang
Kenneth Lange
Chiara Sabatti
机构：
[1] University of California,Department of Statistics
[2] University of California,Department of Human Genetics, Biomathematics and Statistics
[3] Stanford University,Department of Health Research and Policy and Statistics
来源：
BMC Bioinformatics | / 13卷
关键词：
Copy number variant; Copy number polymorphism; Fused lasso; Group fused lasso; MM algorithm;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 395 条
[1]  
Newton MA(2000)Inferring the location and effect of tumor suppressor genes by instability-selection modeling of allelic-loss data Biometrics 56 1088-1097
[2]  
Lee Y(2004)Detection of large-scale variation in the human genome Nat Gene 36 949-951
[3]  
Iafrate AJ(2004)Large-scale copy number polymorphism in the human genome Science 305 525-528
[4]  
Feuk L(2009)Origins and functional impact of copy number variation in the human genome Nature 464 704-712
[5]  
Rivera MN(2008)Genotype, haplotype and copy-number variation in worldwide human populations Nature 451 998-1003
[6]  
Listewnik ML(2011)Mapping copy number variation by population-scale genome sequencing Nature 470 59-65
[7]  
Donahoe PK(2006)Global variation in copy number in the human genome Nature 444 444-454
[8]  
Qi Y(2010)Functional impact of global rare copy number variation in autism spectrum disorders Nature 466 368-372
[9]  
Scherer SW(2008)Large recurrent microdeletions associated with schizophrenia Nature 455 232-236
[10]  
Lee C(2007)QuantiSNP: An objective Bayes hidden-Markov model to detect and accurately map copy number variation using SNP genotyping data Nucleic Acids Res 35 2013-2025
12345678910