Statistical Approaches for Hepatocellular Carcinoma (HCC) Biomarker Discovery
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[1] V. Mazzaferro,et al. Chromosome instability in human hepatocellular carcinoma depends on p53 status and aflatoxin exposure. , 2008, Mutation research.
[2] Gilles Celeux,et al. A statistical approach for CGH microarray data analysis , 2004 .
[3] Kevin P. Murphy,et al. Integrating copy number polymorphisms into array CGH analysis using a robust HMM , 2006, ISMB.
[4] Takehide Asano,et al. Integration of hepatitis B virus DNA into the myeloid/lymphoid or mixed‐lineage leukemia (MLL4) gene and rearrangements of MLL4 in human hepatocellular carcinoma , 2008, Human mutation.
[5] Daniel Pinkel,et al. Genomic microarrays in human genetic disease and cancer. , 2003, Human molecular genetics.
[6] Y. Chung,et al. An Overview of Biomarkers and Molecular Signatures in HCC , 2010, Cancers.
[7] X. Guan,et al. Prognostic significance of c‐myc and AIB1 amplification in hepatocellular carcinoma , 2002, Cancer.
[8] N. Nishida,et al. Discrete breakpoint mapping and shortest region of overlap of chromosome arm 1q gain and 1p loss in human hepatocellular carcinoma detected by semiquantitative microsatellite analysis , 2005, Genes, chromosomes & cancer.
[9] M. S. Mabrouk,et al. K6. Circular binary segmentation modeling of array CGH data on hepatocellular carcinoma , 2012, 2012 29th National Radio Science Conference (NRSC).
[10] Jaakko Astola,et al. CGH-Plotter: MATLAB toolbox for CGH-data analysis , 2003, Bioinform..
[11] R. Scharpf,et al. A multilevel model to address batch effects in copy number estimation using SNP arrays. , 2011, Biostatistics.
[12] Yunyu Zhang,et al. Hidden Markov Model inference copy number change in array-CGH data , 2005 .
[13] Xiaolin Yin,et al. Detecting Copy Number Variations from Array CGH Data Based on a Conditional Random Field Model , 2010, J. Bioinform. Comput. Biol..
[14] Johan Staaf,et al. Continuous-index hidden Markov modelling of array CGH copy number data , 2007, Bioinform..
[15] W. Kuo,et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays , 1998, Nature Genetics.
[16] M. Wigler,et al. Circular binary segmentation for the analysis of array-based DNA copy number data. , 2004, Biostatistics.
[17] R. Eils,et al. Etiology‐dependent molecular mechanisms in human hepatocarcinogenesis , 2007, Hepatology.
[18] Ajay N. Jain,et al. Assembly of microarrays for genome-wide measurement of DNA copy number , 2001, Nature Genetics.
[19] Yi Li,et al. Bayesian Hidden Markov Modeling of Array CGH Data , 2008, Journal of the American Statistical Association.
[20] Krista A. Zanetti,et al. Identification of metastasis‐related microRNAs in hepatocellular carcinoma , 2008, Hepatology.
[21] E. S. Venkatraman,et al. A faster circular binary segmentation algorithm for the analysis of array CGH data , 2007, Bioinform..
[22] J M Trent,et al. Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative genomic hybridization , 2000, Genes, chromosomes & cancer.
[23] Bradley P. Coe,et al. A tiling resolution DNA microarray with complete coverage of the human genome , 2004, Nature Genetics.
[24] Yuedong Wang,et al. Statistical methods for detecting genomic alterations through array-based comparative genomic hybridization (CGH). , 2004, Frontiers in bioscience : a journal and virtual library.
[25] Bauke Ylstra,et al. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high‐resolution microarray comparative genomic hybridization , 2003, The Journal of pathology.
[26] O. Kallioniemi,et al. Genome screening by comparative genomic hybridization. , 1997, Trends in genetics : TIG.
[27] P. Cochat,et al. Et al , 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
[28] N. Nishida,et al. Comprehensive allelotyping of well‐differentiated human hepatocellular carcinoma with semiquantitative determination of chromosomal gain or loss , 2002, Genes, chromosomes & cancer.
[29] S. L. Scott. Bayesian Methods for Hidden Markov Models , 2002 .
[30] John B. Shoven,et al. I , Edinburgh Medical and Surgical Journal.
[31] H. Döhner,et al. Matrix‐based comparative genomic hybridization: Biochips to screen for genomic imbalances , 1997, Genes, chromosomes & cancer.