Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models
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Wenyi Wang | Jonathan Pevsner | Rafael A. Irizarry | Aravinda Chakravarti | Benilton Carvalho | Nathaniel D. Miller | R. Irizarry | A. Chakravarti | B. Carvalho | J. Pevsner | Wenyi Wang
[1] L. Brooks,et al. A DNA polymorphism discovery resource for research on human genetic variation. , 1998, Genome research.
[2] C. Li,et al. Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[3] David M. Rocke,et al. A Model for Measurement Error for Gene Expression Arrays , 2001, J. Comput. Biol..
[4] Martin Vingron,et al. Variance stabilization applied to microarray data calibration and to the quantification of differential expression , 2002, ISMB.
[5] S. P. Fodor,et al. Large-scale genotyping of complex DNA , 2003, Nature Biotechnology.
[6] Rafael A Irizarry,et al. Exploration, normalization, and summaries of high density oligonucleotide array probe level data. , 2003, Biostatistics.
[7] Luc Girard,et al. An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays. , 2004, Cancer research.
[8] Kenny Q. Ye,et al. Large-Scale Copy Number Polymorphism in the Human Genome , 2004, Science.
[9] Rafael A. Irizarry,et al. A Model-Based Background Adjustment for Oligonucleotide Expression Arrays , 2004 .
[10] M. Shapero,et al. High-resolution analysis of DNA copy number using oligonucleotide microarrays. , 2004, Genome research.
[11] Keith W. Jones,et al. Whole genome DNA copy number changes identified by high density oligonucleotide arrays , 2004, Human Genomics.
[12] L. Feuk,et al. Detection of large-scale variation in the human genome , 2004, Nature Genetics.
[13] E. Eichler,et al. Segmental duplications and copy-number variation in the human genome. , 2005, American journal of human genetics.
[14] Hiroyuki Aburatani,et al. Allelic dosage analysis with genotyping microarrays. , 2005, Biochemical and biophysical research communications.
[15] Jing Huang,et al. CARAT: A novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays , 2006, BMC Bioinformatics.
[16] E. Eichler,et al. Fine-scale structural variation of the human genome , 2005, Nature Genetics.
[17] Shigeru Chiba,et al. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. , 2005, Cancer research.
[18] Andrew J Sharp,et al. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome , 2006, Nature Genetics.
[19] D. Conrad,et al. A high-resolution survey of deletion polymorphism in the human genome , 2006, Nature Genetics.
[20] K. Frazer,et al. Common deletions and SNPs are in linkage disequilibrium in the human genome , 2006, Nature Genetics.
[21] K. Gunderson,et al. High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping. , 2006, Genome research.
[22] Jing Huang,et al. Noise Reduction from Genotyping Microarrays Using Probe Level Information , 2006, Silico Biol..
[23] Pardis C Sabeti,et al. Common deletion polymorphisms in the human genome , 2006, Nature Genetics.
[24] Terence P. Speed,et al. Genome analysis A genotype calling algorithm for affymetrix SNP arrays , 2005 .
[25] David Harrington,et al. PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data. , 2007, Biostatistics.
[26] N. Carter,et al. Ultra-high resolution array painting facilitates breakpoint sequencing , 2006, Journal of Medical Genetics.
[27] Rafael A Irizarry,et al. Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data. , 2006, Biostatistics.
[28] Yong-shu He,et al. [Structural variation in the human genome]. , 2009, Yi chuan = Hereditas.