Learning smoothing models of copy number profiles using breakpoint annotations
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F. Bach | Jean-Philippe Vert | T. Hocking | O. Delattre | V. Boeva | I. Janoueix-Lerosey | G. Schleiermacher | Julie Cappo | Olivier Delattre | Francis R. Bach
[1] Read OnlineThe,et al. The Biology of Cancer , 2022, Nature.
[2] Francis R. Bach,et al. Learning Sparse Penalties for Change-point Detection using Max Margin Interval Regression , 2013, ICML.
[3] Toby Dylan Hocking,et al. SegAnnot: an R package for fast segmentation of annotated piecewise constant signals , 2012 .
[4] Jeffrey Heer,et al. D³ Data-Driven Documents , 2011, IEEE Transactions on Visualization and Computer Graphics.
[5] M. Hoebeke,et al. Joint segmentation, calling, and normalization of multiple CGH profiles. , 2011, Biostatistics.
[6] Benjamin J. Raphael,et al. Detection of recurrent rearrangement breakpoints from copy number data , 2011, BMC Bioinformatics.
[7] P. Fearnhead,et al. Optimal detection of changepoints with a linear computational cost , 2011, 1101.1438.
[8] Jean-Philippe Vert,et al. Fast detection of multiple change-points shared by many signals using group LARS , 2010, NIPS.
[9] Gudrun Schleiermacher,et al. Accumulation of segmental alterations determines progression in neuroblastoma. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[10] G. Rigaill. Pruned dynamic programming for optimal multiple change-point detection , 2010, 1004.0887.
[11] Holger Hoefling. A Path Algorithm for the Fused Lasso Signal Approximator , 2009, 0910.0526.
[12] K. Lange,et al. RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. , 2009, The annals of applied statistics.
[13] Achim Zeileis,et al. Collaborative Software Development Using R-Forge , 2009, R J..
[14] Gudrun Schleiermacher,et al. Overall genomic pattern is a predictor of outcome in neuroblastoma. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[15] Polina Golland,et al. Scoring diverse cellular morphologies in image-based screens with iterative feedback and machine learning , 2009, Proceedings of the National Academy of Sciences.
[16] Antonio Torralba,et al. LabelMe: A Database and Web-Based Tool for Image Annotation , 2008, International Journal of Computer Vision.
[17] Yonina C. Eldar,et al. A fast and flexible method for the segmentation of aCGH data , 2008, ECCB.
[18] Antonio Ortega,et al. Sparse representation and Bayesian detection of genome copy number alterations from microarray data , 2008, Bioinform..
[19] David O Siegmund,et al. A Modified Bayes Information Criterion with Applications to the Analysis of Comparative Genomic Hybridization Data , 2007, Biometrics.
[20] E. S. Venkatraman,et al. A faster circular binary segmentation algorithm for the analysis of array CGH data , 2007, Bioinform..
[21] Nigel P. Carter,et al. Accurate and reliable high-throughput detection of copy number variation in the human genome. , 2006, Genome research.
[22] Nicolas Stransky,et al. VAMP: Visualization and analysis of array-CGH, transcriptome and other molecular profiles , 2006, Bioinform..
[23] Kevin P. Murphy,et al. Integrating copy number polymorphisms into array CGH analysis using a robust HMM , 2006, ISMB.
[24] H. Willenbrock,et al. A comparison study: applying segmentation to array CGH data for downstream analyses , 2005, Bioinform..
[25] Marc Lavielle,et al. Using penalized contrasts for the change-point problem , 2005, Signal Process..
[26] Franck Picard,et al. A statistical approach for array CGH data analysis , 2005, BMC Bioinformatics.
[27] Emmanuel Barillot,et al. Analysis of array CGH data: from signal ratio to gain and loss of DNA regions , 2004, Bioinform..
[28] Jean YH Yang,et al. Bioconductor: open software development for computational biology and bioinformatics , 2004, Genome Biology.
[29] W. Kuo,et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays , 1998, Nature Genetics.
[30] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .
[31] Toshiyuki Yamamoto,et al. CONFLICT OF INTEREST: None declared. , 2013 .
[32] R. Tibshirani,et al. Spatial smoothing and hot spot detection for CGH data using the fused lasso. , 2008, Biostatistics.