Description Usage Arguments Value Author(s) See Also Examples
Checks marker redundancy, understood as comcordance between genotypic distributions (including missing values)
1 |
data |
gwaa.data or snp.data object |
pairs |
"bychrom" or "all" to check pairs within chromosome only or genome-wide |
minconcordance |
find "redundant" pairs of markers with concordance >= "minconcordance". If "minconcordance" is more then 1.0, only pairs of markers which are exactly the same (independent of coding), including NA pattern, are considered as redundant. If "minconcordance" is <= 1, the concordance rate is computed as percent of genotypes which are the same, including the genotypes with NA. I.e. if both genotypes are NA, this is counted as a match, if one is NA and other is measured, this is counted as dismatch. Note that option with "minconcordance" <= 1 takes much longer time to run. |
A list containing reference SNP as a name and all SNPs which has "the same" genotypic distribution as values:
"refSNP1" |
SNP11, SNP12, ... |
"refSNP2" |
SNP21, SNP22, ... |
... |
etc. |
"refSNPlast" |
SNPlast1, SNPlast2, ... |
"all" |
list of all redundant SNPs, which can be dropped from consideration |
Yurii Aulchenko
1 2 3 4 |
Loading required package: MASS
Loading required package: GenABEL.data
$all
character(0)
$rs435
[1] "rs455"
$rs663
[1] "rs675"
$rs404
[1] "rs620"
$rs10
[1] "rs29"
$rs611
[1] "rs615"
$rs377
[1] "rs386"
$all
[1] "rs29" "rs128" "rs298" "rs332" "rs361" "rs386" "rs388" "rs455" "rs573"
[10] "rs614" "rs615" "rs620" "rs675"
$rs568
[1] "rs573"
$rs73
[1] "rs128" "rs298" "rs332" "rs614"
$rs348
[1] "rs361"
$rs383
[1] "rs388"
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