# tocID <- "RPR-GEO2R.R"
#
# Purpose:  A Bioinformatics Course:
#              R code accompanying the RPR_GEO2R unit.
#
#
# ==============================================================================
# Version:  1.3
#
# Date:     2017-09  -  2020-09
# Author:   Boris Steipe <boris.steipe@utoronto.ca>
#
# Versions:
#           1.3    use saveRDS()/readRDS() rather than save()/load()
#           1.2    Change from require() to requireNamespace(),
#                      use <package>::<function>() idiom throughout,
#                      use Biocmanager:: not biocLite()
#           1.1    Add section on GPL annotations
#           1.0    Updates for BCH441 2017
#           0.1    First code copied from 2016 material.
#
#
# TODO:
#
#
# == DO NOT SIMPLY  source()  THIS FILE! =======================================
#
# If there are portions you don't understand, use R's help system, Google for an
# answer, or ask your instructor. Don't continue if you don't understand what's
# going on. That's not how it works ...
#
# TO SUBMIT FOR CREDIT....
#
# Note: to submit tasks for credit for this unit, report on the sections
# that have "Task ..." section headers, and report on the lines that are
# identified with #TASK>  comments.
#
# ==============================================================================


#TOC> ==========================================================================
#TOC> 
#TOC>   Section  Title                                                      Line
#TOC> --------------------------------------------------------------------------
#TOC>   1        Preparations                                                 62
#TOC>   2        Loading a GEO Dataset                                        89
#TOC>   2.1        Task - understanding the data                             155
#TOC>   3        Column wise analysis - time points                          164
#TOC>   3.1        Task - Comparison of experiments                          193
#TOC>   3.2        Grouped Samples                                           226
#TOC>   4        Row-wise Analysis: Expression Profiles                      261
#TOC>   4.1        Task - Read a table of features                           296
#TOC>   4.2        Selected Expression profiles                              349
#TOC>   5        Differential Expression                                     392
#TOC>   5.1        Final task: Gene descriptions                             532
#TOC>   6        Improving on Discovery by Differential Expression           538
#TOC>   7        Annotation data                                             633
#TOC> 
#TOC> ==========================================================================


# =    1  Preparations  ========================================================

# To load and analyze GEO datasets we use a number of Bioconductor packages:


if (! requireNamespace("BiocManager", quietly = TRUE)) {
  install.packages("BiocManager")
}

if (! requireNamespace("Biobase", quietly = TRUE)) {
  BiocManager::install("Biobase")
}
# Package information:
#  library(help = Biobase)       # basic information
#  browseVignettes("Biobase")    # available vignettes
#  data(package = "Biobase")     # available datasets


if (! requireNamespace("GEOquery", quietly = TRUE)) {
  BiocManager::install("GEOquery")
}
# Package information:
#  library(help = GEOquery)       # basic information
#  browseVignettes("GEOquery")    # available vignettes
#  data(package = "GEOquery")      # available datasets


# =    2  Loading a GEO Dataset  ===============================================

# The R code below is adapted from the GEO2R scripts produced by GEO for GSE3635
# for the experiment conducted in the BIN-EXPR-GEO unit

# Version info: R 3.2.3, Biobase 2.30.0, GEOquery 2.40.0, limma 3.26.8
# R scripts generated  Wed Jan 11 17:39:46 EST 2017


# Load series and platform data from GEO. The GEO server is a bit flakey and
# I have experienced outages over several hours. If the command below does
# not work for you, skip ahead to the fallback procedure.

GSE3635 <- GEOquery::getGEO("GSE3635", GSEMatrix =TRUE, getGPL=FALSE)
# Note: GEO2R scripts call the expression data set
#       "gset" throughout ... in this script I give
#       it the name "GSE3635" for clarity.

# Subset, if the data contains multiple experiments with different platforms
# since we should not be mixing data from different platforms. (That's
# unfortunately very hard to do correctly). The "platform" is the type of chip
# that was used, and what I selected online when this script was produced, so
# GEO2R knows about the correct platform ID. Technically, subsetting to just one
# platform is not necessary here because we _know_ that GSE3635 contains only
# data produced with the GPL1914 platform. But that's the way GEO2R scripts are
# setup be default since they have to be able to handle a variety of cases.
if (length(GSE3635) > 1) {
  idx <- grep("GPL1914", attr(GSE3635, "names"))
} else {
  idx <- 1
}

GSE3635 <- GSE3635[[idx]]

# FALLBACK
# ... in case the GEO server is not working, load the "GSE3635" object from
# the data directory:
#
# GSE3635 <- readRDS(file="./data/GSE3635.rds")


# Checkpoint ...
if (! exists("GSE3635")) {
  stop("PANIC: GSE3635 was not loaded. Can't continue.")
}


# GSE3635 is an "Expression Set" - cf.
# https://bioconductor.org/packages/release/bioc/vignettes/Biobase/inst/doc/ExpressionSetIntroduction.pdf

# What does this contain?
help("ExpressionSet-class")

# Print it
GSE3635

# Access contents via methods:
Biobase::featureNames(GSE3635)[1:20]   # Rows. What are these features?
Biobase::sampleNames(GSE3635)[1:10]    # Columns. What are these columns?

# Access contents by subsetting:
( tmp <- GSE3635[12:17, 1:6] )

# Access data
Biobase::exprs(tmp)   # exprs() gives us the actual expression values.

# ==   2.1  Task - understanding the data  =====================================

#TASK> What are the data values:
#TASK>  ... in each cell?
#TASK>  ... in each column?
#TASK>  ... in each row?



# =    3  Column wise analysis - time points  ==================================

# Get an overview of the distribution of values in individual columns
summary(Biobase::exprs(GSE3635)[ , 1])
summary(Biobase::exprs(GSE3635)[ , 4])
summary(Biobase::exprs(GSE3635)[ , 7])

# This allows us to com pare the columns, comment on the quality of the data,
# and get a sense for the distribution. We need to know how exactly these
# numbers were produced: obviously, if we don't know how those numbers were
# created in the first place, we would produce a major sin of Cargo Cult
# bioinformatics if we would analyze them.



# compare them in a a boxplot
cyclicPalette <- colorRampPalette(c("#14b4c9",
                                    "#d2d1e6",
                                    "#e66594",
                                    "#d2d1e6",
                                    "#14b4c9",
                                    "#d2d1e6",
                                    "#e66594",
                                    "#d2d1e6",
                                    "#14b4c9"))
tCols <- cyclicPalette(13)
boxplot(Biobase::exprs(GSE3635), col = tCols)


# ==   3.1  Task - Comparison of experiments  ==================================
#TASK>     Study this boxplot. What's going on? Are these expression values?
#TASK>     What do the numbers mean? (Summarize the process and computation
#TASK>     that has gone i to the preprocessing. You need to understand why
#TASK>     these columns all have the same mean and range.) Given what common
#TASK>     sense tells you about the variability of experiments, do you
#TASK>     believe your understanding is complete?


# Lets plot the distributions of values in a more fine-grained manner:
hT0  <- hist(Biobase::exprs(GSE3635)[ ,  1], breaks = 100, col =  tCols[1])
hT3  <- hist(Biobase::exprs(GSE3635)[ ,  4], breaks = 100, col =  tCols[4])
hT6  <- hist(Biobase::exprs(GSE3635)[ ,  7], breaks = 100, col =  tCols[7])
hT9  <- hist(Biobase::exprs(GSE3635)[ , 10], breaks = 100, col =  tCols[10])
hT12 <- hist(Biobase::exprs(GSE3635)[ , 13], breaks = 100, col =  tCols[13])


plot(  hT0$mids,  hT0$counts,  type = "l", col =  tCols[1], xlim = c(-0.5, 0.5))
points(hT3$mids,  hT3$counts,  type = "l", col =  tCols[4])
points(hT6$mids,  hT6$counts,  type = "l", col =  tCols[7])
points(hT9$mids,  hT9$counts,  type = "l", col =  tCols[10])
points(hT12$mids, hT12$counts, type = "l", col =  tCols[13])
legend("topright",
       legend = c("hT0", "hT3", "hT6", "hT9", "hT12"),
       col = tCols[c(1, 4, 7, 10, 13)],
       lwd = 1)


#TASK>   Study this plot. What does it tell you? Is there systematic, global
#TASK>   change in the values over time? Within a cycle? Over the course of the
#TASK>   experiment?


# ==   3.2  Grouped Samples  ===================================================

#  This is the GEO2R code that produces the histogram you saw on the NCBI
#  Website if you went through the BIN-EXPR-GEO unit.

#  Group names for all samples in a series
gsms <- "0123450123450" # Each digit identifies one of the 13 columns
sml <- c()
for (i in 1:nchar(gsms)) {
  sml[i] <- substr(gsms,i,i)
}
sml <- paste("G", sml, sep="")  # set group names

# order samples by group
ex <- Biobase::exprs(GSE3635)[ , order(sml)]
sml <- sml[order(sml)]
fl <- as.factor(sml)
labels <- c("t0","t10","t20","t30","t40","t50") # these are the labels we
                                                # assigned in the BIN-EXPR-GEO
                                                # unit

# Set parameters and draw the plot. I changed this from the original GEO2R
# code which overwrote the global palette(). That's evil! Utility code
# should _never_ mess with global parameters!
GEOcols <- c("#dfeaf4", "#f4dfdf", "#f2cb98", "#dcdaa5",
             "#dff4e4", "#f4dff4",  "#AABBCC")
dev.new(width = 4 + dim(GSE3635)[[2]] / 5, height = 6) # plot into a new window
par(mar = c(2 + round(max(nchar(Biobase::sampleNames(GSE3635))) / 2), 4, 2, 1))
title <- paste ("GSE3635", '/', Biobase::annotation(GSE3635),
                " grouped samples", sep ='')
boxplot(ex, boxwex = 0.6, notch = TRUE, main = title, outline=FALSE,
        las = 2, col = GEOcols[fl])
legend("topleft", labels, fill = GEOcols, bty = "n")


# =    4  Row-wise Analysis: Expression Profiles  ==============================

# What we did above was column-wise analysis and it gave us an idea about how
# our experiments relate to each other. To analyze individual genes, we need to
# do row-wise analyis.

#TASK>  Try to answer the following questions:
#TASK>     Are all rows genes?
#TASK>     What identifiers are being used?
#          (cf. https://sites.google.com/view/yeastgenome-help/community-help/nomenclature-conventions)
#TASK>     Are all rows/genes unique?
#TASK>     Are all yeast genes accounted for?

#     These are crucially important questions but you can't answer the last
#     question  because you have no information other than the gene identifiers.
#     However, any biological interpretation relies absolutely on understanding
#     the semantics of the data. Merely manipulating abstract identifiers and
#     numbers, that would surely be Cargo Cult bioinformatics.

#     To answer these questions about the data semantics, I have provided the
#     file "SGD_features.tab" in the data directory of this project. I have
#     downloaded it from SGD
#     (http://www.yeastgenome.org/download-data/curation), for a description of
#     its contents see here:
file.show("./data/SGD_features.README.txt")
#     Note: the file as downloaded from SGD actually crashed RStudio due to an
#           unbalanced quotation mark which caused R to try and read the whole
#           of the subsequent file into a single string. This was caused by an
#           alias gene name (B"). I have removed this abomination
#           by editing the file. The version in the ./data directory can be
#           read without issues.

# Leets peek into the file:
readLines("./data/SGD_features.tab", n = 5)

# ==   4.1  Task - Read a table of features  ===================================

#      Note: this task asks you to write code. You MUST identify your
#      sources when you draw on other's examples.

# This data file is rather typical of datasets that you will encounter "in the
# wild". To proceed, you need to write code to read it into an R-object. Develop
# the code in your script file according to the following specification:
#
#    -  read "./data/SGD_features.tab" into a data frame
#          called "SGD_features"
#    -  remove unneeded columns - keep the following data columns:
#         -   Primary SGDID
#         -   Feature type
#         -   Feature qualifier
#         -   Feature name - (the systematic name !)
#         -   Standard gene name
#         -   Description
#    -  give the data frame meaningful column names:
#    colnames(SGD_features) <- c("SGDID",
#                                "type",
#                                "qual",
#                                "sysName",
#                                "name",
#                                "description")
#
#    -  remove all rows that don't have a systematic name. (You'll have to check
#          what's in cells that don't have a systematic name)
#    -  check that the systematic names are unique (Hint: use the duplicated()
#          function.)
#    -  assign the systematic names as row names
#    -  confirm: are all rows of the expression data set represented in
#                  the feature table? Hint: use setdiff() to print all that
#                  are not.
#                  Example usage of setdiff():
#                      A <- c("duck", "crow", "gull", "tern")
#                      B <- c("gull", "rook", "tern", "kite", "myna")
#
#                      setdiff(A, B)  #  [1] "duck" "crow"
#                      setdiff(B, A)  #  [1] "rook" "kite" "myna"

#       If some of the features in the expression set are not listed in the
#       systematic names, you have to be aware of that, when you try to get
#       more information on them. I presume they are missing because revisions
#       of the yeast genome after these experiments were done showed that these
#       genes did not actually exist.

#    -  confirm: how many / which genes in the feature table do not
#                have expression data?

#  How should we handle rows/columns that are missing or not unique?


# ==   4.2  Selected Expression profiles  ======================================

# The code below assumes that you have read ./data/SGD_features.tab and assigned
# the resulting data frame to SGD_features, with columns as specified above.

# Here is an expression profile for Mbp1.

gName <- "MBP1"
(iFeature <- which(SGD_features$name == gName))
(iExprs   <- which(featureNames(GSE3635) == SGD_features$sysName[iFeature]))
plot(seq(0, 120, by = 10),
     Biobase::exprs(GSE3635)[iExprs, ],
     main = paste("Expression profile for", gName),
     xlab = "time (min)",
     ylab = "expression",
     type = "b",
     col= "maroon")
abline(h =  0, col = "#00000055")
abline(v = 60, col = "#00000055")

# Print the description
SGD_features$description[iFeature]

# Here is a list of gene names that may be involved in the cell cycle switch,
# and some genes that are controls (cf. BIN-SYS-Concepts):

# Turning it on
# Cdc14, Mbp1, Swi6, Swi4, Whi5, Cdc28, Cln1, Cln2, Cln3

# Turning it off
# Rad53, Cdc28, Clb1, Clb2, Clb6, Nrm1

# Housekeeping genes
# Act1, and Alg9

#TASK>  Plot expression profiles for these genes and study them. What do you
#TASK>  expect the profiles to look like, given the role of these genes? What
#TASK>  do you find? (Hint: you will make your life much easier if you define
#TASK>  a function that plots and prints descriptions with a gene name as input.
#TASK>  Also: are the gene names in the feature table upper case, or lower case?
#TASK>  Also: note that the absolute values of change are quite different.
#TASK>  Also: note that some values may be outliers i.e. failed experiments.)

# =    5  Differential Expression  =============================================

# GEO2R discovers the top differentially expressed  expressed genes by
# using functions in the Bioconductor limma package.

if (! requireNamespace("limma", quietly = TRUE)) {
  BiocManager::install("limma")
}
# Package information:
#  library(help = limma)       # basic information
#  browseVignettes("limma")    # available vignettes
#  data(package = "limma")     # available datasets

# The GEO2R limma code is virtually uncommented, and has not been written for
# clarity, but for being easily produced by a code-generator that is triggered
# by the parameters on the GEO Web-site. Most of it is actually dispensable for
# our purposes.

# In principle, the code goes through three steps:
# 1. Prepare the data
# 2. Define groups that are to be contrasted to define "Differential"
# 3. Find genes whose expression levels are significantly different across
#     the groups
# 4. Format results.

# Biobase is a highly engineered package that is tightly integrated into
# the Bioconductor world - unfortunately that brings with it a somewhat
# undesirable level of computational overhead and dependencies. Using the
# package as we normally do - i.e. calling required functions with their
# explicit package prefix is therefore not advisable. There are generics
# that won't be propery dispatched. If you only need a small number of
# functions for a very specific context, you will probably get away with
# Biobase::<function>() - but even in the demonstration code of this script
# not everything works out of the box. We'll therefore load the library,
# but we'll (redundantly) use the prefix anyway so as to emphasize where
# the functions come from.

library(Biobase)

# We are recapitulating the experiment in which we assigned the 0, 10, 60 and
# 70 minute samples to one group, the 30, 40, 90 and 100 minute samples to
# another group, and calculated differential expression values between these
# two groups.

setA <- c(1, 2, 7, 8)    # columns for set A
setB <- c(4, 5, 10, 11)  # columns for set B

# We remove columns we don't need, and for simplicity put the experiments for
# group A in the first four columns, and the group B in the next four.

mySet <- GSE3635[ , c(setA, setB)]

# limma needs the column descriptions as factors
mySet$description <- as.factor(c(rep("A", 4), rep("B", 4)))

# Next we build the "design Matrix" for the statistical test:
myDesign <- model.matrix(~ description + 0, mySet)
colnames(myDesign) <- levels(mySet$description)
myDesign

# Now we can calculate the fit of all rows to a linear model that depends
# on the two groups as specified in the design:
myFit <- limma::lmFit(mySet, myDesign)

# Next we calculate the contrasts, given the fit ...
myCont.matrix <- limma::makeContrasts(A - B, levels = myDesign)
myFit2 <- limma::contrasts.fit(myFit, myCont.matrix)

# ... compute appropriate probabilites from a modified t-test
#     (empirical Bayes) ...
myFit2 <- limma::eBayes(myFit2, 0.01)

# ... add the gene names to the fit - object ...
myFit2$genes <- featureNames(mySet)

# ... and pick the top N differentially expressed genes while controlling
#     for multiple testing with a False Discovery Rate (fdr) correction. GEO2R
#     gave us only the top 250 genes, but we might as well do 1000, just so we
#     can be reasonable sure that our gens of interest are included.
N <- 1000
myTable <- limma::topTable(myFit2,
                           adjust.method = "fdr",
                           sort.by = "B",
                           number = N)

str(myTable)
# The gene names are now in the $ID column

# These are the top 10
write.table(myTable[1:10 , c("ID","P.Value","B")],
            file = stdout(),
            row.names = FALSE,
            sep="\t")

# Let's see what we got: let's plot the full expression profiles (all 13
# columns) for the top ten genes from exprs(GSE3635).

plot(seq(0, 120, by = 10),
     rep(0, 13),
     type = "n",
     ylim = c(-1, 1),
     xlab = "time",
     ylab = "log-ratio expression")
rect( 0,  -2,  15, 2, col = "#dfeaf4", border = NA)   # setA
rect( 55, -2,  75, 2, col = "#dfeaf4", border = NA)   # setA
rect( 25, -2,  45, 2, col = "#f4dfdf", border = NA)   # setB
rect( 85, -2, 105, 2, col = "#f4dfdf", border = NA)   # setB
abline(h = 0, col = "#00000055")

for (i in 1:10) {
  thisID <- myTable$ID[i]
  points(seq(0, 120, by = 10), Biobase::exprs(GSE3635)[thisID, ], type = "b")
}

# Our guess that we might discover interesting genes by selecting groups A and B
# like we did was not bad. But limma knows nothing about the biology and though
# the expression profiles look good, there is no guarantee that these are the
# most biologically relevant genes. Significantly different in expression
# according to the groups we define is not necessarily the same as a cyclically
# varying gene, nor does it necessarily find the genes whose expression levels
# are _most_ different, i.e. if the variance of a highly, differentially
# expressed gene within a group is large, it may not be very significant. Also,
# we are not exploiting the fact that these values are time series.
# Nevertheless, we find genes for which we see a change in expression levels
# along two cell-cycles.

# Let's superimpose some "real" cell-cycle genes:
myControls <- c("Cdc14", "Mbp1", "Swi6", "Swi4", "Whi5", "Cln1", "Cln2", "Cln3")
for (name in toupper(myControls)) {
  thisID <- SGD_features$sysName[which(SGD_features$name == name)]
  points(seq(0, 120, by=10),
         Biobase::exprs(GSE3635)[thisID, ],
         type="b",
         col="#AA0000")
}

# Indeed, the discovered gene profiles look much "cleaner" than the real cycle
# genes and this just means that differential expression in the way that we
# have performed it is an approximation to the biology.

# ==   5.1  Final task: Gene descriptions  =====================================

#TASK> Print the descriptions of the top ten differentially expressed genes
#TASK> and comment on what they have in common (or not).


# =    6  Improving on Discovery by Differential Expression  ===================


# There are many ways to improve on purely statistical methods, if we have
# better ideas about the biology. I would just like to demonstrate one
# possibility here: calculate correlation values to a sample gene - such as Cln2
# for which we know that it is involved in the cell cycle. Let's plot it first:

gName <- "CLN2"
(iFeature <- which(SGD_features$name == gName))
(iExprs   <- which(featureNames(GSE3635) == SGD_features$sysName[iFeature]))
Cln2Profile <- Biobase::exprs(GSE3635)[iExprs, ]
plot(seq(0, 120, by = 10),
     Cln2Profile,
     ylim = c(-1, 1),
     main = paste("Expression profile for", gName),
     xlab = "time (min)",
     ylab = "expression",
     type = "b",
     pch = 16,
     cex = 1.5,
     lwd = 2,
     col= "#40b886")
abline(h =  0, col = "#0000FF55")
abline(v = 60, col = "#0000FF55")

# Set up a vector of correlation values


myCorrelations <- numeric(nrow(Biobase::exprs(GSE3635)))
names(myCorrelations) <- Biobase::featureNames(GSE3635)
for (i in 1:length(myCorrelations)) {
  myCorrelations[i] <- cor(Cln2Profile, Biobase::exprs(GSE3635)[i, ])
}

nTOP <- 20
myTopC <- order(myCorrelations, decreasing = TRUE)[1:nTOP]

# Number 1
(ID <- Biobase::featureNames(GSE3635)[myTopC[1]])

# Get information
SGD_features[which(SGD_features$sysName == ID), ]
# Of course: the highest correlation is Cln1 itself. This is our positive
# control for the experiment.

# Let's plot the rest
myPal <- colorRampPalette(c("#82f58d", "#E0F2E2", "#f6f6f6"))

for (i in 2:nTOP) {
  ID <- Biobase::featureNames(GSE3635)[myTopC[i]]
  points(seq(0, 120, by = 10),
         Biobase::exprs(GSE3635)[ID, ],
       type = "b",
       cex = 0.8,
       col= myPal(nTOP)[i])
  print(SGD_features[which(SGD_features$sysName == ID),
                     c("name", "description")])
}

# Note that all of these genes are highly correlated with a known cell cycle
# gene, but because the absolute values of expression differences are not very
# large for some of them, they might not be picked up by any algorithm that is
# focussed on large differential expression changes. Do small relative changes
# mean small biological effects? Certainly not!

# And we haven't even looked at the anticorrelated genes yet...
nBOT <- nTOP
myBottomC <- order(myCorrelations, decreasing = FALSE)[1:nBOT]  # bottom ten
myPal <- colorRampPalette(c("#ba112a", "#E3C8CC", "#ebebeb"))

for (i in 1:nBOT) {
  ID <- Biobase::featureNames(GSE3635)[myBottomC[i]]
  points(seq(0, 120, by = 10),
         Biobase::exprs(GSE3635)[ID, ],
         type = "b",
         cex = 0.8,
         col= myPal(nBOT)[i])
  print(SGD_features[which(SGD_features$sysName == ID),
                     c("name", "description")])
}
# ... which are very interesting in their own right.

# What I hope you appreciate from this example is:
#   -  convenient general purpose methods exist that analyze expression data
#        with sophisticated statistical methods;
#   -  the results of these methods depend on whether the statistics model
#        the biology well;
#   -  you will draw Cargo Cult conclusions if you can't cast your biology
#        of interest in terms of a model, "canned" solutions are unlikely
#        to give you all the answers you need;
#   -  being able to write your own code gives you the freedom to experiment
#        and explore. There is a learning curve - but the payoffs are
#        significant.

# =    7  Annotation data  =====================================================
#
# Loading feature data "by hand" as we've done above, is usually not necessary
# since GEO provides rich annotations in the GPL platform files, which are
# associated with its Gene Expression Sets files. In the code above,
# we used getGEO("GSE3635", GSEMatrix = TRUE, getGPL = FALSE), and the GPL
# annotations were not loaded. We could use getGPL = TRUE instead ...

GSE3635annot <- GEOquery::getGEO("GSE3635", GSEMatrix = TRUE, getGPL = TRUE)
GSE3635annot <- GSE3635annot[[1]]

# ... and the feature data is then available in the GSE3635@featureData@data
#     slot:
str(GSE3635annot@featureData@data)
GSE3635annot@featureData@data[ 1:20 , ]

# ... from where you can access the columns you need, e.g. spotIDs and gene
#     symbols:

myAnnot <- GSE3635annot@featureData@data[ , c("SPOT_ID", "Gene")]
str(myAnnot)

# ... Note that this is a data frame and it is easy to find things we
#  might be looking for ...
myAnnot[which(myAnnot$Gene == "MBP1"), ]

# ... or identify rows that might give us trouble, such as probes that
#     hybridize to more than one gene.


# Alternatively, we could have identified the GPL file for this set:
GSE3635@annotation   # "GPL1914"

# ... and downloaded it directly from NCBI:
GPL1914 <- GEOquery::getGEO("GPL1914")
str(GPL1914)

# ... from which we can get the data - which is however NOT necessarily
# matched to the rows of our expression dataset.


# [END]