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Statistics for ChIP-chip and DNase hypersensitivity experiments on NimbleGen arrays
Peter C Scacheri1, Gregory E Crawford, Sean Davis
1Department of Genetics, Case Western Reserve University, Cleveland, OH, USA.
Methods in Enzymology
|August 31, 2006
Summary
A new program, ACME (Algorithm for Capturing Microarray Enrichment), analyzes high-density oligonucleotide tiling array data. This tool identifies genomic signals in ChIP-chip and DNase-chip experiments, aiding researchers in data interpretation.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- High-density oligonucleotide tiling arrays generate complex data requiring specialized analysis.
- Existing methods for analyzing tiled array data present computational challenges for researchers.
Purpose of the Study:
- To introduce ACME (Algorithm for Capturing Microarray Enrichment), a novel computational program for analyzing NimbleGen-tiled microarray data.
- To provide a robust method for identifying significant genomic regions from ChIP-chip and DNase-chip experiments.
Main Methods:
- ACME employs a sliding window and threshold strategy to detect signal enrichment (peaks) in tiled array data.
- The program assigns a probability value (p-value) to each probe, enabling statistical assessment of identified signals.
- The software is implemented in the R language and is available through Bioconductor.
Main Results:
- ACME successfully identifies genomic signals in both ChIP-chip and DNase-chip applications.
- The algorithm provides a p-value for each probe, facilitating the statistical validation of enriched regions.
- Recommendations for data quality assessment and ACME optimization are provided.
Conclusions:
- ACME offers an effective solution for analyzing high-density oligonucleotide tiling array data.
- The program aids in the interpretation of ChIP-chip and DNase-chip data, advancing genomic research.
- ACME is a freely available bioinformatics tool for the scientific community.

