Description Details Author(s) References See Also Examples
Deconvolution of Chromatin-IP-to-microarray (ChIP-chip) data to identify
binding sites at high resolution across the genome.
To be published in Bioinformatics and submitted to Bioconductor.
This package includes all data described in the manuscript.
Package: | MeDiChI |
Type: | Package |
Version: | 0.1-4 |
Date: | 2007-11-25 |
License: | GPL version 3 |
demo(MeDiChI)
David J Reiss, Institute for Systems Biology
Maintainer: <dreiss@systemsbiology.org>
(1). Reiss, DJ and Facciotti, MT and Baliga, NS. (2007). "Model-based
deconvolution of genome-wide DNA binding",
Bioinformatics; doi: 10.1093/bioinformatics/btm592. http://baliga.systemsbiology.net/medichi
(2) Qi, Y and et al. (2006). "High-resolution computational models of genome
binding events", Nature Biotechnol, 24(8), 963-970. http://cgs.csail.mit.edu/jbd.
chip.deconv, deconv.entire.genome, fit.peak.profile, generate.fake.data,
generate.binding.profile, MeDiChI-data,
<lars>
, <quadprog>
, <Matrix>
1 2 3 4 5 6 7 8 9 10 11 | demo( MeDiChI )
## Run the demo yourself:
data( "halo.lowres", package="MeDiChI" )
fit <- chip.deconv( data.halo.lowres, where="Chr", fit.res=30,
center=650000, wind=20000, max.steps=100, n.boot=10,
kernel=kernel.halo.lowres, verbose=TRUE, boot.sample.opt="case" )
coef( fit ) ## Print out the coefficients
plot( fit, plot.genes=TRUE, cex=0.5, cex.lab=0.8, cex.axis=0.8 )
|
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