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  1. 1
    ENmix: a novel background correction method for Illumina HumanMethylation450 BeadChip

    ENmix: a novel background correction method for Illumina HumanMethylation450 BeadChip de réir Zongli Xu, Liang Niu, Leping Li, Jack A. Taylor

    Foilsithe / Cruthaithe 2015
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  2. 2
    <scp>MicroRNA</scp> levels are modulated in <i><scp>A</scp>edes aegypti</i> after exposure to <scp>D</scp>engue‐2

    <scp>MicroRNA</scp> levels are modulated in <i><scp>A</scp>edes aegypti</i> after exposure to <scp>D</scp>engue‐2 de réir Corey L. Campbell, Tabitha A. Harrison, Ann M. Hess, G. D. Ebel

    Foilsithe / Cruthaithe 2013
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  3. 3
    Chromatin segmentation based on a probabilistic model for read counts explains a large portion of the epigenome

    Chromatin segmentation based on a probabilistic model for read counts explains a large portion of the epigenome de réir Alessandro Mammana, Ho‐Ryun Chung

    Foilsithe / Cruthaithe 2015
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  4. 4
    How to build personalized multi-omics comorbidity profiles

    How to build personalized multi-omics comorbidity profiles de réir Mohammad Ali Moni, Píetro Lió

    Foilsithe / Cruthaithe 2015
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  5. 5
    Spatial normalization of array-CGH data

    Spatial normalization of array-CGH data de réir Pierre Neuvial, Philippe Hupé, Isabel Martínez Brito, Stéphane Liva, Élodie Manié, Caroline Brennetot, François Radvanyi, Alain Aurias, Emmanuel Barillot

    Foilsithe / Cruthaithe 2006
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  6. 6
    Detection of differentially methylated regions from whole-genome bisulfite sequencing data without replicates

    Detection of differentially methylated regions from whole-genome bisulfite sequencing data without replicates de réir Hao Wu, Tianlei Xu, Hao Feng, Li Chen, Ben Li, Bing Yao, Zhaohui Qin, Peng Jin, Karen N. Conneely

    Foilsithe / Cruthaithe 2015
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  7. 7
    Empirical array quality weights in the analysis of microarray data

    Empirical array quality weights in the analysis of microarray data de réir Matthew E. Ritchie, Dileepa Diyagama, Jody Neilson, Ryan K. van Laar, Alexander Dobrovic, Andrew J. Holloway, Gordon K. Smyth

    Foilsithe / Cruthaithe 2006
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  8. 8
    The Analysis of Gene Expression Data: Methods and Software

    The Analysis of Gene Expression Data: Methods and Software de réir Thomas Boyle

    Foilsithe / Cruthaithe 2005
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  9. 9
    A guide to genome‐wide association analysis and post‐analytic interrogation

    A guide to genome‐wide association analysis and post‐analytic interrogation de réir Eric Reed, Sara Núñez, David Kulp, Jing Qian, Muredach P. Reilly, Andrea S. Foulkes

    Foilsithe / Cruthaithe 2015
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  10. 10
    Analysis of cell-based RNAi screens

    Analysis of cell-based RNAi screens de réir Michael Boutros, Lı́gia P. Brás, Wolfgang Huber

    Foilsithe / Cruthaithe 2006
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  11. 11
    EMDomics: a robust and powerful method for the identification of genes differentially expressed between heterogeneous classes

    EMDomics: a robust and powerful method for the identification of genes differentially expressed between heterogeneous classes de réir Sheida Nabavi, Daniel Schmolze, Mayinuer Maitituoheti, Sadhika Malladi, Andrew H. Beck

    Foilsithe / Cruthaithe 2015
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  12. 12
    ToPASeq: an R package for topology-based pathway analysis of microarray and RNA-Seq data

    ToPASeq: an R package for topology-based pathway analysis of microarray and RNA-Seq data de réir Ivana Ihnatová, Eva Budínská

    Foilsithe / Cruthaithe 2015
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  13. 13
    diffHic: a Bioconductor package to detect differential genomic interactions in Hi-C data

    diffHic: a Bioconductor package to detect differential genomic interactions in Hi-C data de réir Aaron T. L. Lun, Gordon K. Smyth

    Foilsithe / Cruthaithe 2015
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  14. 14
    quantro: a data-driven approach to guide the choice of an appropriate normalization method

    quantro: a data-driven approach to guide the choice of an appropriate normalization method de réir Stephanie C. Hicks, Rafael A. Irizarry

    Foilsithe / Cruthaithe 2015
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  15. 15
    Modeling of RNA-seq fragment sequence bias reduces systematic errors in transcript abundance estimation

    Modeling of RNA-seq fragment sequence bias reduces systematic errors in transcript abundance estimation de réir Michael I. Love, John B. Hogenesch, Rafael A. Irizarry

    Foilsithe / Cruthaithe 2016
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  16. 16
    Interpretation of multiple probe sets mapping to the same gene in Affymetrix GeneChips

    Interpretation of multiple probe sets mapping to the same gene in Affymetrix GeneChips de réir Maria A. Stalteri, Andrew Harrison

    Foilsithe / Cruthaithe 2007
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  17. 17
    CompGO: an R package for comparing and visualizing Gene Ontology enrichment differences between DNA binding experiments

    CompGO: an R package for comparing and visualizing Gene Ontology enrichment differences between DNA binding experiments de réir Ashley J. Waardenberg, Samuel D. Bassett, Romaric Bouveret, Richard P. Harvey

    Foilsithe / Cruthaithe 2015
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  18. 18
    INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments

    INSPEcT: a computational tool to infer mRNA synthesis, processing and degradation dynamics from RNA- and 4sU-seq time course experiments de réir Stefano de Pretis, Theresia Kreß, Marco J. Morelli, Giorgio Melloni, Laura Riva, Bruno Amati, Mattia Pelizzola

    Foilsithe / Cruthaithe 2015
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  19. 19
    DiffVar: a new method for detecting differential variability with application to methylation in cancer and aging

    DiffVar: a new method for detecting differential variability with application to methylation in cancer and aging de réir Belinda Phipson, Alicia Oshlack

    Foilsithe / Cruthaithe 2014
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  20. 20
    Exploring Massive, Genome Scale Datasets with the GenometriCorr Package

    Exploring Massive, Genome Scale Datasets with the GenometriCorr Package de réir Alexander V. Favorov, Loris Mularoni, Leslie Cope, Yulia A. Medvedeva, Andrey A. Mironov, Vsevolod J. Makeev, Sarah J. Wheelan

    Foilsithe / Cruthaithe 2012
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