Description Usage Arguments Details Value Author(s) References See Also Examples
Calculate read-enrichment scores for each nucleotide position
1 | ChIPseqScore(control, sample, backg = -1, file = NA, norm = 3 * 10^9, test = "Ratio",times=1e6,digits=2)
|
control |
data.frame structure obtained by mappedReads2Nhits |
sample |
data.frame structure obtained by mappedReads2Nhits |
backg |
Due low coverage in the control, there could be regions with no hits. Any region with a hit value lower than |
file |
Name of the file where you wan to save the results (if desired) |
norm |
Integer value. Number of hits will be reported by number of hits per |
test |
Use a score based on the poisson distribution ("Poisson") or in the ratio ("Ratio") |
times |
To be memory efficient, CSAR will only upload to the RAM memory fragments of length |
digits |
Number of decimal digits used to report the score values |
Different sequencing efforts yield different number of sequenced reads, for this reason the "number of hits" at each nucleotide position is normalized by the total number of nucleotides sequenced.
Subsequently, the number of hits for the sample is normalize to have the same mean and variance than the control, for each chromosome independently or for the whole set of chromosomes (depending of the value of normEachChrInd
).
Due low coverage, there could be regions with no hits. Any region with a hit value lower than backg
in the control
will be set to the value of backg
For each nucleotide position, a read-enrichment score will be calculated with the Poisson test, or with the ratio.
A list to be used for other functions of the CSAR package
chr |
Chromosme names |
chrL |
Chromosme length (bp) |
filenames |
Name of the files where the score values are storaged |
digits |
Score values storaged on the files need to be divided by 10^ |
Jose M Muino, jose.muino@wur.nl
Muino et al. (submitted). Plant ChIP-seq Analyzer: An R package for the statistical detection of protein-bound genomic regions.
Kaufmann et al.(2009).Target genes of the MADS transcription factor SEPALLATA3: integration of developmental and hormonal pathways in the Arabidopsis flower. PLoS Biology; 7(4):e1000090.
CSAR-package
1 2 3 4 5 6 7 8 9 | ##For this example we will use the a subset of the SEP3 ChIP-seq data (Kaufmann, 2009)
data("CSAR-dataset");
##We calculate the number of hits for each nucleotide posotion for the control and sample. We do that just for chromosome chr1, and for positions 1 to 10kb
nhitsS<-mappedReads2Nhits(sampleSEP3_test,file="sampleSEP3_test",chr=c("CHR1v01212004"),chrL=c(10000))
nhitsC<-mappedReads2Nhits(controlSEP3_test,file="controlSEP3_test",chr=c("CHR1v01212004"),chrL=c(10000))
##We calculate a score for each nucleotide position
test<-ChIPseqScore(control=nhitsC,sample=nhitsS)
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