Description Usage Arguments Value
findGenesInterval
Use the mapping position (inferred) of each gene to
find potential candidates under a QTL confidence interval
1 2 3 | findGenesInterval(findGenecM.output = NULL, calcCis.output = NULL,
qtlname = NULL, chr, lowposition, highposition, geneID, geneChr,
geneBp, genecM)
|
findGenecM.output |
Output from findGenecM If supplied, geneID, geneChr, geneBp and genecM are ignored |
calcCis.output |
Output from calcCis. If supplied, chr, lowposition and highposition are ignored |
qtlname |
Identifier of each qtl |
chr |
QTL Chromosome |
lowposition |
Lower confidence interval bound (cM) |
highposition |
Upper confidence interval bound (cM) |
geneID |
The name of each gene |
geneChr |
The chromosome of each gene |
geneBp |
The basepair position of each gene (not currently in use) |
genecM |
The mapping position of each gene |
... |
Not currently in use. |
A named list where each element corresponds to a provided QTL confidence interval. Character vectors in each element display potential candidate genes for each QTL.
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