Literature DB >> 19957145

R classes and methods for SNP array data.

Robert B Scharpf1, Ingo Ruczinski.   

Abstract

The Bioconductor project is an "open source and open development software project for the analysis and comprehension of genomic data" (1), primarily based on the R programming language. Infrastructure packages, such as Biobase, are maintained by Bioconductor core developers and serve several key roles to the broader community of Bioconductor software developers and users. In particular, Biobase introduces an S4 class, the eSet, for high-dimensional assay data. Encapsulating the assay data as well as meta-data on the samples, features, and experiment in the eSet class definition ensures propagation of the relevant sample and feature meta-data throughout an analysis. Extending the eSet class promotes code reuse through inheritance as well as interoperability with other R packages and is less error-prone. Recently proposed class definitions for high-throughput SNP arrays extend the eSet class. This chapter highlights the advantages of adopting and extending Biobase class definitions through a working example of one implementation of classes for the analysis of high-throughput SNP arrays.

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Mesh:

Year:  2010        PMID: 19957145      PMCID: PMC2853754          DOI: 10.1007/978-1-60327-194-3_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  10 in total

1.  Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.

Authors:  Xiaojun Di; Hajime Matsuzaki; Teresa A Webster; Earl Hubbell; Guoying Liu; Shoulian Dong; Dan Bartell; Jing Huang; Richard Chiles; Geoffrey Yang; Mei-mei Shen; David Kulp; Giulia C Kennedy; Rui Mei; Keith W Jones; Simon Cawley
Journal:  Bioinformatics       Date:  2005-01-18       Impact factor: 6.937

2.  A genotype calling algorithm for affymetrix SNP arrays.

Authors:  Nusrat Rabbee; Terence P Speed
Journal:  Bioinformatics       Date:  2005-11-02       Impact factor: 6.937

3.  Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data.

Authors:  Benilton Carvalho; Henrik Bengtsson; Terence P Speed; Rafael A Irizarry
Journal:  Biostatistics       Date:  2006-12-22       Impact factor: 5.899

4.  SNPchip: R classes and methods for SNP array data.

Authors:  Robert B Scharpf; Jason C Ting; Jonathan Pevsner; Ingo Ruczinski
Journal:  Bioinformatics       Date:  2007-01-04       Impact factor: 6.937

Review 5.  Methods and strategies for analyzing copy number variation using DNA microarrays.

Authors:  Nigel P Carter
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

6.  Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays.

Authors:  Robert B Scharpf; Giovanni Parmigiani; Jonathan Pevsner; Ingo Ruczinski
Journal:  Ann Appl Stat       Date:  2008-06-01       Impact factor: 2.083

7.  PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data.

Authors:  Thomas Laframboise; David Harrington; Barbara A Weir
Journal:  Biostatistics       Date:  2006-06-20       Impact factor: 5.899

8.  A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.

Authors:  Yasuhito Nannya; Masashi Sanada; Kumi Nakazaki; Noriko Hosoya; Lili Wang; Akira Hangaishi; Mineo Kurokawa; Shigeru Chiba; Dione K Bailey; Giulia C Kennedy; Seishi Ogawa
Journal:  Cancer Res       Date:  2005-07-15       Impact factor: 12.701

9.  Bioconductor: open software development for computational biology and bioinformatics.

Authors:  Robert C Gentleman; Vincent J Carey; Douglas M Bates; Ben Bolstad; Marcel Dettling; Sandrine Dudoit; Byron Ellis; Laurent Gautier; Yongchao Ge; Jeff Gentry; Kurt Hornik; Torsten Hothorn; Wolfgang Huber; Stefano Iacus; Rafael Irizarry; Friedrich Leisch; Cheng Li; Martin Maechler; Anthony J Rossini; Gunther Sawitzki; Colin Smith; Gordon Smyth; Luke Tierney; Jean Y H Yang; Jianhua Zhang
Journal:  Genome Biol       Date:  2004-09-15       Impact factor: 13.583

10.  CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.

Authors:  Jing Huang; Wen Wei; Joyce Chen; Jane Zhang; Guoying Liu; Xiaojun Di; Rui Mei; Shumpei Ishikawa; Hiroyuki Aburatani; Keith W Jones; Michael H Shapero
Journal:  BMC Bioinformatics       Date:  2006-02-21       Impact factor: 3.169

  10 in total
  1 in total

1.  ReadqPCR and NormqPCR: R packages for the reading, quality checking and normalisation of RT-qPCR quantification cycle (Cq) data.

Authors:  James R Perkins; John M Dawes; Steve B McMahon; David L H Bennett; Christine Orengo; Matthias Kohl
Journal:  BMC Genomics       Date:  2012-07-02       Impact factor: 3.969

  1 in total

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