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Bioinformatics and Computational Biology Solutions Using R and Bioconductor

Robert Gentleman ; Vincent J. Carey ; Wolfgang Huber ; Rafael A. Irizarry ; Sandrine Dudoit (eds.)

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No disponible.

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Institución detectada Año de publicación Navegá Descargá Solicitá
No detectada 2005 SpringerLink

Información

Tipo de recurso:

libros

ISBN impreso

978-0-387-25146-2

ISBN electrónico

978-0-387-29362-2

Editor responsable

Springer Nature

País de edición

Reino Unido

Fecha de publicación

Información sobre derechos de publicación

© Springer Science+Business Media, Inc. 2005

Tabla de contenidos

Bioconductor Software for Graphs

V. J. Carey; R. Gentleman; W. Huber; J. Gentry

We describe software tools for creating, manipulating, and visualizing graphs in the Bioconductor project. We give the rationale for our design decisions and provide brief outlines of how to make use of these tools. The discussion mirrors that of Chapter 20 where the different mathematical constructs were described. It is worth differentiating between packages that are mainly infrastructure (sets of tools that can be used to create other pieces of software) and packages that are designed to provide an end-user application. The packages graph, RBGL, and Rgraphviz are infrastructure packages. Software developers may use these packages to construct tools aimed at specific applications areas, such as the GOstats package.

Palabras clave: Short Path; Random Graph; Minimal Span Tree; Edge Weight; Short Path Algorithm.

Part IV - Graphs and networks | Pp. 347-368

Case Studies Using Graphs on Biological Data

R. Gentleman; D. Scholtens; B. Ding; V. J. Carey; W. Huber

In this chapter we consider four specific data-analytic and inferential problems that can be addressed using graphs. We demonstrate the use of the software and methods described in Chapters 20 and 21 on real problems in computational biology.We will show how one can investigate relationships between gene expression and protein-protein interaction data, how GO annotations can be used to analyze gene sets, how literature citations can be related to experimental data, and how gene expression data can be mapped on pathways.

Palabras clave: Bipartite Graph; Edge Weight; Jaccard Index; Expression Cluster; Permute Graph.

Part IV - Graphs and networks | Pp. 369-394

limma: Linear Models for Microarray Data

G. K. Smyth

A survey is given of differential expression analyses using the linear modeling features of the limma package. The chapter starts with the simplest replicated designs and progresses through experiments with two or more groups, direct designs, factorial designs and time course experiments. Experiments with technical as well as biological replication are considered. Empirical Bayes test statistics are explained. The use of quality weights, adaptive background correction and control spots in conjunction with linear modelling is illustrated on the β7 data.

Palabras clave: Design Matrix; Background Correction; Limma Package; Control Spot; Target Frame.

Part V - Case studies | Pp. 397-420

Classification with Gene Expression Data

M. Dettling

A survey is given of tasks related to the construction and evaluation of classifiers applied to a renal cell cancer data set. Balanced sample splitting, non-specific filtering, linear discriminant analysis, nearest-neighbor prediction, and support vector machines are all concretely illustrated using the MLInterfaces package. Evaluations based on single and multiple random splits of data are compared. The entire presentation is given in a very generic programming format, to facilitate the adaptation and variation, by other investigators, of the techniques used here.

Palabras clave: Support Vector Machine; Linear Discriminant Analysis; Prediction Rule; Class Prediction; Variable Selection Procedure.

Part V - Case studies | Pp. 421-430

From CEL Files to Annotated Lists of Interesting Genes

R. A. Irizarry

One of the most popular applications of microarray technology is the identification of genes that are differentially expressed in two populations.With Affymetrix GeneChip technology, there are several steps between hybridization and the selection of interesting genes. The steps of preprocessing to improve signal to noise ratios, choosing a summary statistic for appropriate ranking of genes, and deciding on a final filter for candidate genes are largely statistical in nature. In this chapter, we demonstrate Bioconductor tools useful for creating such lists. We start from the raw probe level data (CEL files) and conclude with the creation of annotated reports.

Palabras clave: Interesting Gene; Volcano Plot; Average Fold Change; Probe Level Data; False Discovery Rate Adjustment.

Part V - Case studies | Pp. 431-442