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rxSeq (version 0.99.3)

rcX: Reformatted data for chromosome X set to be used as input to process function

Description

This is an object of type readCounts provides with example of experimental data for a subset of X chromosome genes. The full model requires a combination of total read counts (y) - all the reads belonging for a gene, and finding out which of these reads we can specifically attribute to allele A or allele B - allele specific counts (n), separately the reads attributed specifically to allele B (n0B). Also, tausB - is the Xce effect for each F1 mouse, which specifies the proportion of allele specific reads belonging to allele B. Also, it includes the other data pieces to fit the model: kappas - total number of counts for each mouse, on log scale, index - specifying which cross each mouse belongs to, and geneids - Ensembl ids of genes. They, as well as the datasets simulated with simRX can be fitted using process with appropriate options chrom="X" and field model to be either "full" or "short".

Arguments

Value

genes.switch=genes.switch, geneids=geneids,

See Also

process,readCounts,simRX.

Examples

Run this code
# see total read counts (TReC) for first 2 X chromosome genes of a data example:
rcX

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