Nothing
if (interactive()) savehistory();
library("aroma.affymetrix");
library("R.menu");
verbose <- Verbose(threshold=-10, timestamp=TRUE);
options(width=60);
chipType <- "GenomeWideSNP_6";
cdfTags <- "Full";
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# User settings
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
## setOption(aromaSettings, "user/initials", "HB");
## setOption(aromaSettings, "user/fullname", "Henrik Bengtsson");
## obf <- sprintf("%s@%s", "henrik.bengtsson", "aroma-project.org");
## setOption(aromaSettings, "user/email", obf);
## saveAnywhere(aromaSettings);
fullname <- getOption(aromaSettings, "user/fullname");
stopifnot(!is.null(fullname));
email <- getOption(aromaSettings, "user/email");
stopifnot(!is.null(email));
user <- getOption(aromaSettings, "user/initials");
stopifnot(!is.null(user));
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# Settings
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
genomeVersions <- c("30"="hg18", "31"="hg19");
naVersions <- names(genomeVersions);
choices <- sprintf("na%s (%s)", naVersions, genomeVersions);
choice <- textMenu(choices, title="Choose NetAffx version: ", value=FALSE);
naVersion <- naVersions[choice];
genomeVersion <- genomeVersions[naVersion];
datestamp <- format(Sys.Date(), format="%Y%m%d");
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# Setup required annotation files
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
cdf <- AffymetrixCdfFile$byChipType(chipType, tags=cdfTags);
rm(csvList);
print(cdf);
csvList <- list();
tagsList <- c(
main=sprintf(".na%s", naVersion),
cn=sprintf(".cn.na%s", naVersion)
);
for (key in names(tagsList)) {
tags <- tagsList[[key]];
pathname <- AffymetrixNetAffxCsvFile$findByChipType(chipType, tags=tags);
if (isFile(pathname)) {
csvList[[key]] <- AffymetrixNetAffxCsvFile(pathname);
}
rm(tags);
}
print(csvList);
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# Import UGP from CSV files
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
tags <- sprintf("na%s,%s,%s%s", naVersion, genomeVersion, user, datestamp);
ugp <- NULL;
tryCatch({
ugp <- AromaUgpFile$byChipType(getChipType(cdf), tags=tags);
}, error = function(ex) {})
if (is.null(ugp)) {
ugp <- AromaUgpFile$allocateFromCdf(cdf, tags=tags);
}
print(ugp);
for (kk in seq_along(csvList)) {
csv <- csvList[[kk]];
print(csv);
units <- importFrom(ugp, csv, verbose=verbose);
str(units);
## GenomeWideSNP_6.na<XX>.annot.csv: int [1:934968] 334945 334944 ...
## GenomeWideSNP_6.cn.na<XX>.annot.csv: int [1:945826] 935622 935777 ...
}
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# Update the file footer
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
srcFileTags <- list();
srcFiles <- c(list(cdf), csvList);
for (kk in seq_along(srcFiles)) {
srcFile <- srcFiles[[kk]];
tags <- list(
filename=getFilename(srcFile),
filesize=getFileSize(srcFile),
checksum=getChecksum(srcFile)
);
srcFileTags[[kk]] <- tags;
}
print(srcFileTags);
footer <- readFooter(ugp);
footer$createdBy <- list(
fullname = fullname,
email = email
);
names(srcFileTags) <- sprintf("srcFile%d", seq_along(srcFileTags));
footer$srcFiles <- srcFileTags;
writeFooter(ugp, footer);
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# Statistics
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
print(ugp);
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# WHAT'S NEW:
#
# o na30 -> na31
# Lots of changes, especially large changes in positions.
# o na27.1 -> na30
# No differences
# o na27 -> na27.1
# No differences
# o na26 -> na27
# Two units (932039, 1872834) where moved from ChrX to ChrY.
# Same location.
# o na24 -> na26
# Only minor modifications for non-missing values:
# - three loci changed chromosomes
# - an additional 23 loci changed positions, of which only 17 moved
# more than 2 base pairs.
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
ugp <- AromaUgpFile$byChipType("GenomeWideSNP_6,Full", tags="na31");
ugp0 <- AromaUgpFile$byChipType("GenomeWideSNP_6,Full", tags="na30");
print(table(ugp[,1], exclude=NULL));
print(table(ugp0[,1], exclude=NULL));
## GenomeWideSNP_6,Full,na31,hg19,HB20110328
## 1 2 3 4 5 6 7 8
## 146626 153717 127767 120377 115735 112727 100925 98308
## 9 10 11 12 13 14 15 16
## 82300 93635 89598 87341 65927 57115 53596 54111
## 17 18 19 20 21 22 23 24
## 46609 52102 30365 43649 25105 24438 87271 9688
## 25 <NA>
## 455 1928
## GenomeWideSNP_6,na30,hg18,HB20100215.ugp
## 1 2 3 4 5 6 7 8
## 146401 153663 127766 120296 115672 112825 100996 98277
## 9 10 11 12 13 14 15 16
## 82168 93592 89525 87321 66067 57103 53556 54182
## 17 18 19 20 21 22 23 24
## 46632 52093 30299 43628 25111 24484 87200 9483
## 25 <NA>
## 445 2630
rr <- whichVector(ugp[,1] != ugp0[,1]);
str(rr);
## integer(0)
rr <- whichVector(ugp[,2] != ugp0[,2]);
str(rr);
## integer(0)
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