theta.aa, theta.ab, theta.bb should have columns equal to the number of samples in the batch
git-svn-id: file:///home/git/hedgehog.fhcrc.org/bioconductor/trunk/madman/Rpacks/crlmm@59943 bc3139a8-67e5-0310-9ffc-ced21a209358
... | ... |
@@ -63,7 +63,8 @@ getFeatureData <- function(cdfName, copynumber=FALSE){ |
63 | 63 |
M[index, "isSnp"] <- 0L |
64 | 64 |
} |
65 | 65 |
##A few of the snpProbes do not match -- I think it is chromosome Y. |
66 |
- M[is.na(M[, "chromosome"]), "isSnp"] <- 1L |
|
66 |
+ if(any(is.na(M[, "chromosome"]))) |
|
67 |
+ M[is.na(M[, "chromosome"]), "isSnp"] <- 1L |
|
67 | 68 |
M <- data.frame(M) |
68 | 69 |
return(new("AnnotatedDataFrame", data=M)) |
69 | 70 |
} |
... | ... |
@@ -1383,9 +1384,6 @@ imputeCenterX <- function(muA, muB, Ns, index.complete, MIN.OBS){ |
1383 | 1384 |
} |
1384 | 1385 |
|
1385 | 1386 |
|
1386 |
- |
|
1387 |
- |
|
1388 |
- |
|
1389 | 1387 |
## constructors for Illumina platform |
1390 | 1388 |
constructIlluminaFeatureData <- function(gns, cdfName){ |
1391 | 1389 |
pkgname <- paste(cdfName, "Crlmm", sep="") |
... | ... |
@@ -1406,6 +1404,8 @@ constructIlluminaFeatureData <- function(gns, cdfName){ |
1406 | 1404 |
data=data.frame(mapping), |
1407 | 1405 |
varMetadata=data.frame(labelDescription=colnames(mapping))) |
1408 | 1406 |
} |
1407 |
+ |
|
1408 |
+ |
|
1409 | 1409 |
constructIlluminaAssayData <- function(np, snp, object, storage.mode="environment", nr){ |
1410 | 1410 |
stopifnot(identical(snp$gns, featureNames(object))) |
1411 | 1411 |
gns <- c(featureNames(object), np$gns) |
... | ... |
@@ -1669,7 +1669,8 @@ summarizeSnps <- function(strata, |
1669 | 1669 |
index.list, |
1670 | 1670 |
object, |
1671 | 1671 |
GT.CONF.THR, |
1672 |
- verbose, CHR.X, ...){ |
|
1672 |
+ verbose, |
|
1673 |
+ CHR.X, ...){ |
|
1673 | 1674 |
## if(is.lds) { |
1674 | 1675 |
## physical <- get("physical") |
1675 | 1676 |
## open(object) |
... | ... |
@@ -2776,6 +2777,9 @@ calculateRTheta <- function(cnSet, genotype=c("AA", "AB", "BB"), batch.name){ |
2776 | 2777 |
x[x < 64] <- 64 |
2777 | 2778 |
y[y < 64] <- 64 |
2778 | 2779 |
theta[, "theta"] <- atan2(y, x)*2/pi |
2780 |
+ if(any(is.na(theta))){ |
|
2781 |
+ stop("NA's in thetas. Can not compute theta / R values for batches with fewer than 10 samples") |
|
2782 |
+ } |
|
2779 | 2783 |
## so that 'R' is available for NP probes |
2780 | 2784 |
y[is.na(y)] <- 0 |
2781 | 2785 |
theta[, "R"] <- x+y |
... | ... |
@@ -540,11 +540,12 @@ setMethod("calculateRBaf", signature(object="CNSet"), |
540 | 540 |
RTheta.ab <- calculateRTheta(object, "AB", batch.name) |
541 | 541 |
RTheta.bb <- calculateRTheta(object, "BB", batch.name) |
542 | 542 |
|
543 |
- theta.aa <- matrix(RTheta.aa[, "theta"], nrow(object), ncol(object), byrow=FALSE) |
|
544 |
- theta.ab <- matrix(RTheta.ab[, "theta"], nrow(object), ncol(object), byrow=FALSE) |
|
545 |
- theta.bb <- matrix(RTheta.bb[, "theta"], nrow(object), ncol(object), byrow=FALSE) |
|
546 |
- |
|
547 | 543 |
J <- which(batch(object) == batch.name) |
544 |
+ |
|
545 |
+ theta.aa <- matrix(RTheta.aa[, "theta"], nrow(object), length(J), byrow=FALSE) |
|
546 |
+ theta.ab <- matrix(RTheta.ab[, "theta"], nrow(object), length(J), byrow=FALSE) |
|
547 |
+ theta.bb <- matrix(RTheta.bb[, "theta"], nrow(object), length(J), byrow=FALSE) |
|
548 |
+ |
|
548 | 549 |
a <- A(object)[, J, drop=FALSE] |
549 | 550 |
b <- B(object)[, J, drop=FALSE] ## NA's for b where nonpolymorphic |
550 | 551 |
dns <- dimnames(a) |
... | ... |
@@ -74,7 +74,8 @@ pathToCels <- "/thumper/ctsa/snpmicroarray/hapmap/raw/affy/1m" |
74 | 74 |
if(getRversion() < "2.13.0"){ |
75 | 75 |
rpath <- getRversion() |
76 | 76 |
} else rpath <- "trunk" |
77 |
-outdir <- paste("/amber1/archive/oncbb/rscharpf/crlmm_vignette/", rpath, sep="") |
|
77 |
+##outdir <- paste("/amber1/archive/oncbb/rscharpf/crlmm_vignette/", rpath, sep="") |
|
78 |
+outdir <- paste("/amber1/archive/oncbb/rscharpf/crlmm_vignette/", rpath, "/gw6v1.5/", sep="") |
|
78 | 79 |
dir.create(outdir, recursive=TRUE, showWarnings=FALSE) |
79 | 80 |
@ |
80 | 81 |
|