## Abstract Two‐color cDNA or oligonucleotide‐based spotted microarrays have been commonly used in measuring the expression levels of thousands of genes simultaneously. To realize the immense potential of this powerful new technology, budgeted within limited resources or other constraints, practica
Experimental designs for 2-colour cDNA microarray experiments
✍ Scribed by Nam-Ky Nguyen; E. R. Williams
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 233 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1524-1904
- DOI
- 10.1002/asmb.654
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Kerr and Churchill (Biostatistics 2001; 2:183–201) showed how varieties (e.g. type of tissues, drug treatments, etc.) are paired onto arrays by a catalogue of A‐optimal incomplete block designs (IBDs) for 6–10 varieties (v), and number of blocks of size 2 between v and $ \left(v \atop 2 \right)$. These A‐optimal IBDs were obtained by (i) generating all non‐isomorphic connected graphs on v vertices using Brendan McKay's, MAKEG program (http://cs.anu.edu.au/people/bdm/nauty/) and (ii) comparing all designs of the same size on the basis of A‐optimality to obtain the best ones.
In this paper we will give a quick overview on IBDs and describe an algorithmic approach to extend the mentioned catalogue. We aim at IBDs with up to 100 varieties with equal as well as unequal replications. A catalogue of 2007 IBDs is given. We will also extend the concept of even designs in Kerr and Churchill (Biostatistics 2001; 2:183–201) to row‐orthogonal designs. Copyright © 2006 John Wiley & Sons, Ltd.
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