Conditional random pattern model for copy number aberration detection
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[1] Christian A. Rees,et al. Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[2] M. Delforge. Understanding the pathogenesis of myelodysplastic syndromes. , 2003, The hematology journal : the official journal of the European Haematology Association.
[3] C. Chang,et al. Multiple distinct clones may co-exist in different lineages in myelodysplastic syndromes. , 2009, Leukemia research.
[4] Hiroyuki Aburatani,et al. Allelic dosage analysis with genotyping microarrays. , 2005, Biochemical and biophysical research communications.
[5] Xiaojin Zhu,et al. Kernel conditional random fields: representation and clique selection , 2004, ICML.
[6] U. Germing,et al. Validation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients. , 2000, Leukemia research.
[7] R. Tibshirani,et al. A method for calling gains and losses in array CGH data. , 2005, Biostatistics.
[8] Lawrence R. Rabiner,et al. A tutorial on hidden Markov models and selected applications in speech recognition , 1989, Proc. IEEE.
[9] Charles Lee,et al. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. , 2006, Genome research.
[10] C. Yau,et al. QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data , 2007, Nucleic acids research.
[11] E. S. Venkatraman,et al. A faster circular binary segmentation algorithm for the analysis of array CGH data , 2007, Bioinform..
[12] W. Kuo,et al. Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene , 2000, Nature Genetics.
[13] P. Nguyen,et al. Myelodysplastic syndromes , 2009, Nature Reviews Disease Primers.
[14] M. Wigler,et al. Circular binary segmentation for the analysis of array-based DNA copy number data. , 2004, Biostatistics.
[15] Fred A. Wright,et al. Integrated study of copy number states and genotype calls using high-density SNP arrays , 2009, Nucleic acids research.
[16] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[17] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[18] D. Schaid. Mathematical and Statistical Methods for Genetic Analysis , 1999 .
[19] Jane Fridlyand,et al. Erratum: "Hidden Markov models approach to the analysis of array CGH data" (Journal of Multivariate Analysis (2004) vol. 90 (132-153) 10.1016/j.jmva.2004.02.008) , 2005 .
[20] Emmanuel Barillot,et al. Analysis of array CGH data: from signal ratio to gain and loss of DNA regions , 2004, Bioinform..
[21] Åsa Hedman,et al. SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data , 2005, Nucleic acids research.
[22] T. LaFramboise,et al. SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samples. , 2008, American journal of human genetics.
[23] Sarah Barber,et al. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation. , 2006, American journal of human genetics.
[24] Shigeru Chiba,et al. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. , 2005, Cancer research.
[25] D. Hanahan,et al. The Hallmarks of Cancer , 2000, Cell.
[26] Andrew McCallum,et al. Dynamic conditional random fields: factorized probabilistic models for labeling and segmenting sequence data , 2004, J. Mach. Learn. Res..
[27] Peter J. Park,et al. Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data , 2005, Bioinform..
[28] Joseph T. Glessner,et al. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. , 2007, Genome research.
[29] R. Redon,et al. Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes , 2007, Science.
[30] Ajay N. Jain,et al. Hidden Markov models approach to the analysis of array CGH data , 2004 .
[31] Cheng Li,et al. Automating dChip: toward reproducible sharing of microarray data analysis , 2008, BMC Bioinformatics.
[32] Joshua M. Korn,et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs , 2008, Nature Genetics.
[33] S. Kajigaya,et al. Distinctive gene expression profiles of CD34 cells from patients with myelodysplastic syndrome characterized by specific chromosomal abnormalities. , 2004, Blood.
[34] Marc A. Attiyeh,et al. Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. , 2008, Genome research.
[35] Marco A. Marra,et al. Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data , 2007, BMC Bioinformatics.
[36] Jr. G. Forney,et al. Viterbi Algorithm , 1973, Encyclopedia of Machine Learning.
[37] Marc A. Attiyeh,et al. Erratum: Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy (Genome Research (2009) 19 (276-283)) , 2009 .
[38] 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.
[39] Andrew McCallum,et al. Conditional Random Fields: Probabilistic Models for Segmenting and Labeling Sequence Data , 2001, ICML.
[40] E. Thiel,et al. Therapeutic spectrum in the treatment of myelodysplastic syndromes , 2004, Expert opinion on pharmacotherapy.