Intermediate Phylotranscriptomics Analyses

Flat Line Test

The Flat Line Test is a permutation test quantifying the statistical significance of an observed phylotranscriptomic pattern. The goal is to detect any evolutionary signal within a developmental time course that significantly deviates from a flat line.

To build the test statistic we start with a standard PhyloExpressionSet. The myTAI package provides an example PhyloExpressionSet named PhyloExpressionSetExample:

library(myTAI)

# load an example PhyloExpressionSet stored in the myTAI package
data(PhyloExpressionSetExample) 

# look at the standardized data set format
head(PhyloExpressionSetExample, 3) 

  Phylostratum      GeneID   Zygote Quadrant Globular     Heart  Torpedo      Bent    Mature
1            1 at1g01040.2 2173.635 1911.200 1152.555 1291.4224 1000.253  962.9772 1696.4274
2            1 at1g01050.1 1501.014 1817.309 1665.309 1564.7612 1496.321 1114.6435 1071.6555
3            1 at1g01070.1 1212.793 1233.002  939.200  929.6195  864.218  877.2060  894.8189

Users will observe that the first column of the PhyloExpressionSetExample stores the Phylostratum assignments of the corresponding genes. The permutation test is based on random sampling of the Phylostratum assignment of genes. The underlying assumption is that the TAI profile of correctly assigned Phylostrata is significantly deviating from TAI profiles based on randomly assigned Phylostrata.

# TAI profile of correctly assigned Phylostrata
TAI(PhyloExpressionSetExample) 

  Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature 
3.229942 3.225614 3.107135 3.116693 3.073993 3.176511 3.390334

Visualization:

data(PhyloExpressionSetExample)
# Visualize the TAI profile of correctly assigned Phylostrata
PlotSignature( ExpressionSet = PhyloExpressionSetExample, 
               p.value       = FALSE ) 

  Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature 
3.543700 3.573999 3.554707 3.543376 3.582905 3.562813 3.523409 

Visualization:

# Visualize the TAI profile based on randomly assigned Phylostrata
PlotSignature( ExpressionSet =  randomPhyloExpressionSetExample, 
               p.value       = FALSE ) 

Users will observe that the visual pattern of the correctly assigned TAI profile and the randomly assigned TAI profile differ qualitatively.

Now we investigate the variance of the two observed patterns.

[1] 0.01147725

[1] 0.0004102549

We observe that the variance of the randomly assigned TAI profile is much smaller than the variance of the correctly assigned TAI profile. Here we use the variance to quantify the flatness of a given TAI profile. In theory the variance of a perfect flat line would be zero. So any TAI profile that is close to zero would resemble a flat line. But how exactly are the variances of randomly assigned TAI profiles distributed? For this purpose the bootMatrix() function was implemented.

The bootMatrix() takes an PhyloExpressionSet or DivergenceExpressionSet as input and computes N TAI or TDI profiles based on randomly assigned Phylostrata or Divergence-Strata.

    Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature
1 3.578000 3.577732 3.552230 3.556756 3.555627 3.553580 3.510978
2 3.590339 3.564544 3.589012 3.598754 3.583721 3.597553 3.633530
3 3.615284 3.616286 3.569486 3.566816 3.575761 3.554789 3.601522
4 3.501172 3.506554 3.486261 3.491282 3.531536 3.541634 3.494997
5 3.450857 3.458339 3.447274 3.463692 3.444261 3.468433 3.497926
6 3.539454 3.543827 3.595298 3.588149 3.582898 3.588062 3.565487

Based on this booMatrix we can compute the variance of each random TAI profile.

# compute the variance of the random TAI profile for each row
variance_vector <- apply(randomTAIs, 1 , var)

# and visualize the distribution of variances
hist(variance_vector, breaks = 100)

Now it is interesting to see where we can find the variance of the correctly assigned TAI.

# variance of the TAI profile based on correctly assigned Phylostrata
var_real <- var(TAI(PhyloExpressionSetExample)) 

# visualize the distribution of variances
hist( x      = c(variance_vector,var_real), 
      breaks = 100, 
      xlab   = "variance", 
      main   = "Histogram of variance_vector" )

# and plot a red line at the position where we can find the 
# real variance
abline(v = var_real, lwd = 5, col = "red")

This plot illustrates that variances based on random TAI profiles seem to have a smaller variance than the variance based on the correct TAI profile. To obtain a p-value that now quantifies this difference, we need to fit the histogram of variance_vector with a specific probability distribution.

Visually it would be possible to choose a gamma distribution to fit the histogram of variance_vector. To validate this choice a Cullen and Frey graph provided by the fitdistrplus package can be used.

# install.packages("fitdistrplus")

# plot a Cullen and Frey graph
fitdistrplus::descdist(variance_vector)

Based on the observation that a gamma distribution is a suitable fit for variance_vector, we can now estimate the parameters of the gamma distribution that fits the data.

# estimate the parameters: shape and rate using 'moment matching estimation'
gamma_MME <- fitdistrplus::fitdist(variance_vector,distr = "gamma", method = "mme")
# estimate shape:
shape <- gamma_MME$estimate[1]
# estimate the rate:
rate <- gamma_MME$estimate[2]

# define an expression written as function as input for the curve() function
gamma_distr <- function(x){ return(dgamma(x = x, shape = shape, rate = rate)) }

# plot the density function and the histogram of variance_vector
curve( expr = gamma_distr,
       xlim = c(min(variance_vector),max(c(variance_vector,var_real))),
       col  = "steelblue",
       lwd  = 5,
       xlab = "Variances", 
       ylab = "Frequency" )

# plot the histogram of variance_vector
histogram <- hist(variance_vector,prob = TRUE,add = TRUE, breaks = 100)
rug(variance_vector)

# plot a red line at the position where we can find the real variance
abline(v = var_real, lwd = 5, col = "red")

Using the gamma distribution with estimated parameters the corresponding p-value of var_real can be computed.

# p-value of var_real
pgamma(var_real, shape = shape,rate = rate, lower.tail = FALSE)

Hence, the variance of the correct TAI profile significantly deviates from random TAI profiles and this allows us to assume that the underlying TAI profile captures a real evolutionary signal.

Using the FlatLineTest() Function

This entire procedure of computing the p-value having the variance of TAI profiles as test statistic is done by the FlatLineTest() function.

# Perform the FlatLineTest
FlatLineTest( ExpressionSet = PhyloExpressionSetExample, 
              permutations  = 1000 )

This function returns the p-value of the test statistic.

Additionally the FlatLineTest() function allows to investigate the goodness of the test statistic.

# perform the FlatLineTest and investigate the goodness of the test statistic
FlatLineTest( ExpressionSet = PhyloExpressionSetExample, 
              permutations  = 1000, 
              plotHistogram = TRUE )

The plotHistogram argument specifies whether analytics plots shall be drawn to quantify the goodness of the test statistic returned by the FlatLineTest.

The three resulting plots show:

• a Cullen and Frey graph

• a histogram of the test statistic and the corresponding gamma distribution that was fitted to the test statistic

• a plot showing the p-values (p_flt) for 10 individual runs. Since the underlying test statistic is generated by a permutation test, the third plot returned by FlatLineTest() shows the influence of different permutations to the corresponding p-value

In other words, to test whether or not the underlying permutation of the permutation test is causing the significance of the p-value, you can specify the runs argument within the FlatLineTest() function to perform several independent runs. In case there exists a permutation that causes a previous significant p-value to become non-significant, the corresponding phylotranscriptomic pattern shouldn’t be considered as statistically significant.

Reductive Hourglass Test

The Reductive Hourglass Test has been developed to statistically evaluate the existence of a phylotranscriptomic hourglass pattern based on TAI or TDI computations. The corresponding p-value quantifies the probability that a given TAI or TDI pattern (or any phylotranscriptomics pattern) does not follow an hourglass like shape. A p-value < 0.05 indicates that the corresponding phylotranscriptomics pattern does indeed follow an hourglass (high-low-high) shape.

To build the test statistic again we start with a standard PhyloExpressionSet.

  Phylostratum      GeneID   Zygote Quadrant Globular     Heart  Torpedo      Bent    Mature
1            1 at1g01040.2 2173.635 1911.200 1152.555 1291.4224 1000.253  962.9772 1696.4274
2            1 at1g01050.1 1501.014 1817.309 1665.309 1564.7612 1496.321 1114.6435 1071.6555
3            1 at1g01070.1 1212.793 1233.002  939.200  929.6195  864.218  877.2060  894.8189

And again compute the TAI() profile of the PhyloExpressionSetExample.

# TAI profile of correctly assigned Phylostrata
TAI(PhyloExpressionSetExample) 

  Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature 
3.229942 3.225614 3.107135 3.116693 3.073993 3.176511 3.390334 

Visualization:

# visualize the TAI profile of correctly assigned Phylostrata
PlotSignature( ExpressionSet = PhyloExpressionSetExample, 
               p.value       = FALSE ) 

The Reductive Hourglass Test is a permutation test based on the following test statistic.

1. A set of developmental stages is partitioned into three modules - early, mid, and late - based on prior biological knowledge (see Drost et al., 2015 for details).

2. The mean TAI or TDI value for each of the three modules \(T_{early}\), \(T_{mid}\), and \(T_{late}\) are computed.

3. The two differences D1 = \(T_{early}\) - \(T_{mid}\) and D2 = \(T_{late}\) - \(T_{mid}\) are calculated.

4. The minimum \(D_{min}\) of D1 and D2 is computed as final test statistic of the Reductive Hourglass Test.

In order to determine the statistical significance of an observed minimum difference \(D_{min}\) the following permutation test was performed. Based on the bootMatrix() \(D_{min}\) is calculated from each of the permuted TAI or TDI profiles, approximated by a Gaussian distribution with method of moments estimated parameters returned by fitdistrplus::fitdist(), and the corresponding p-value is computed by pnorm given the estimated parameters of the Gaussian distribution. The goodness of fit for the random vector \(D_{min}\) is statistically quantified by a Lilliefors (Kolmogorov-Smirnov) test for normality.

To perform the Reductive Hourglass Test you can use the ReductiveHourglassTest() function. Using this function you need to divide the given phylotranscriptomic pattern into three developmental modules:

• early module
• mid module
• late module

This can be done using the modules argument: module = list(early = 1:2, mid = 3:5, late = 6:7). In this example (PhyloExpressionSetExample) we divide the corresponding developmental process into the three modules:

• early module: Stages 1 - 2 = Zygote and Quadrant
• mid module: Stages 3 - 5 = Globular, Heart, and Torpedo
• late module: Stages 6 - 7 = Bent and Mature

# Perform the Reductive Hourglass Test
ReductiveHourglassTest( ExpressionSet = PhyloExpressionSetExample,
                        modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                        lillie.test   = TRUE ) 

The corresponding output shows the p-value returned by the Reductive Hourglass Test, the standard deviation of randomly permuted TAI profiles returned by bootMatrix() (apply(bootMatrix(PhyloExpressionSetExample) , 2 , sd)) and in case the argument lillie.test = TRUE, a logical value representing the goodness of fit statistic returned by the Lilliefors (Kolmogorov-Smirnov) test for normality. In case lillie.test is TRUE the corresponding Lilliefors (Kolmogorov-Smirnov) test passed the goodness of fit criterion. In case lillie.test is FALSE the corresponding goodness of fit by a normal distribution is not statistically significant.

Analogous to the plotHistogram argument that is present in the FlatLineTest() function, the ReductiveHourglassTest() function also takes an argument plotHistogram. When plotHistogram = TRUE, the ReductiveHourglassTest() function returns a multi-plot showing:

• A Cullen and Frey skewness-kurtosis plot. This plot illustrates which distributions seem plausible to fit the resulting permutation vector \(D_{min}\). Here a normal distribution seems most plausible.

• A histogram of \(D_{min}\) combined with the density plot is visualized. \(D_{min}\) is then fitted by a normal distribution. The corresponding parameters are estimated by moment matching estimation.

• A plot showing the p-values for N independent runs to verify that a specific p-value is biased by a specific permutation order.

• A bar plot showing the number of cases in which the underlying goodness of fit (returned by Lilliefors (Kolmogorov-Smirnov) test for normality) has shown to be significant (TRUE) or not significant (FALSE). This allows to quantify the permutation bias and their implications on the goodness of fit.

# perform the Reductive Hourglass Test and plot the test statistic
ReductiveHourglassTest( ExpressionSet = PhyloExpressionSetExample,
                        modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                        plotHistogram = TRUE, 
                        lillie.test   = TRUE ) 

The corresponding output shows the summary statistics of the fitted normal distribution as well as the p-value, standard deviation, and Lilliefors (Kolmogorov-Smirnov) test result.

This example output nicely illustrates that although the Lilliefors (Kolmogorov-Smirnov) test for normality is violated for some permutations, the Cullen and Frey graph shows that there is no better approximation than a normal distribution (which is also supported visually by investigating the fitted frequency distribution). The corresponding p-value returned by ReductiveHourglassTest() is significant and illustrates that the observed phylotranscriptomic pattern of PhyloExpressionSetExample does follow the Hourglass Model assumption.

Reductive Early Conservation Test

The Early Conservation Test has been developed to statistically evaluate the existence of a monotonically increasing phylotranscriptomic pattern based on TAI or TDI computations. The corresponding p-value quantifies the probability that a given TAI or TDI pattern (or any phylotranscriptomic pattern) does not follow an early conservation like pattern. A p-value < 0.05 indicates that the corresponding phylotranscriptomics pattern does indeed follow an early conservation (low-high-high) shape.

To build the test statistic again we start with a standard PhyloExpressionSet.

library(myTAI)

# load an example PhyloExpressionSet stored in the myTAI package
data(PhyloExpressionSetExample) 

# look at the standardized data set format
head(PhyloExpressionSetExample, 3) 

And again compute the TAI() profile of the PhyloExpressionSetExample.

# TAI profile of correctly assigned Phylostrata
TAI(PhyloExpressionSetExample) 

  Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature 
3.229942 3.225614 3.107135 3.116693 3.073993 3.176511 3.390334

Visualization:

# Visualize the TAI profile of correctly assigned Phylostrata
PlotSignature( ExpressionSet = PhyloExpressionSetExample, 
               p.value       = FALSE ) 

The reductive early conservation test is a permutation test based on the following test statistic.

1. A set of developmental stages is partitioned into three modules - early, mid, and late - based on prior biological knowledge.

2. The mean TAI or TDI value for each of the three modules \(T_{early}\), \(T_{mid}\), and \(T_{late}\) are computed.

3. The two differences D1 = \(T_{mid}\) - \(T_{early}\) and D2 = \(T_{late}\) - \(T_{early}\) are calculated.

4. The minimum \(D_{min}\) of D1 and D2 is computed as final test statistic of the Reductive Early Conservation Test.

In order to determine the statistical significance of an observed minimum difference \(D_{min}\) the following permutation test was performed. Based on the bootMatrix() \(D_{min}\) is calculated from each of the permuted TAI or TDI profiles, approximated by a Gaussian distribution with method of moments estimated parameters returned by fitdistrplus::fitdist(), and the corresponding p-value is computed by pnorm given the estimated parameters of the Gaussian distribution. The goodness of fit for the random vector \(D_{min}\) is statistically quantified by an Lilliefors (Kolmogorov-Smirnov) test for normality.

To perform the Reductive Early Conservation Test you can use the EarlyConservationTest() function. Using this function you need to divide the given phylotranscriptomics pattern into three developmental modules:

• early module
• mid module
• late module

This can be done using the modules argument: module = list(early = 1:2, mid = 3:5, late = 6:7). In this example (PhyloExpressionSetExample) we divide the corresponding developmental process into the three modules:

• early module: Stages 1 - 2 = Zygote and Quadrant
• mid module: Stages 3 - 5 = Globular, Heart, and Torpedo
• late module: Stages 6 - 7 = Bent and Mature

# Perform the Reductive Early Conservation Test
EarlyConservationTest( ExpressionSet = PhyloExpressionSetExample,
                       modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                       lillie.test   = TRUE ) 

Analogous to the plotHistogram argument that is present in the FlatLineTest() and ReductiveHourglassTest() function, the EarlyConservationTest() function also takes an argument plotHistogram. When plotHistogram = TRUE, the EarlyConservationTest() function returns a multi-plot showing:

• A Cullen and Frey skewness-kurtosis plot. This plot illustrates which distributions seem plausible to fit the resulting permutation vector \(D_{min}\). Again a normal distribution seems most appropriate.

• A histogram of \(D_{min}\) combined with the density plot is visualized. \(D_{min}\) is then fitted by a normal distribution. The corresponding parameters are estimated by moment matching estimation.

• A plot showing the p-values for N independent runs to verify that a specific p-value is biased by a specific permutation order.

• A bar plot showing the number of cases in which the underlying goodness of fit (returned by Lilliefors (Kolmogorov-Smirnov) test for normality) has shown to be significant (TRUE) or not significant (FALSE). This allows to quantify the permutation bias and their implications on the goodness of fit.

# perform the Reductive Early Conservation Test and plot the test statistic
EarlyConservationTest( ExpressionSet = PhyloExpressionSetExample,
                       modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                       plotHistogram = TRUE, 
                       lillie.test   = TRUE ) 

This example output nicely illustrates that although the Lilliefors (Kolmogorov-Smirnov) test for normality is violated, the Cullen and Frey graph shows that there is no better approximation than a normal distribution (which is also supported visually by investigating the fitted frequency distribution). The corresponding p-value returned by the EarlyConservationTest() is highly non-significant and illustrates that the observed phylotranscriptomic pattern of PhyloExpressionSetExample does not follow the Early Conservation Model assumption.

This example shall illustrate that finding the right test statistic is a multi-step process of investigating different properties of the underlying permutation test. Although single aspects might fit or fit not corresponding criteria, the overall impression (sum of all individual analyses) must be considered to obtain a valid p-value.

Reverse Hourglass Test

The Reverse Hourglass Test has been developed to statistically evaluate the existence of a reverse hourglass pattern based on TAI or TDI computations. The corresponding p-value quantifies the probability that a given TAI or TDI pattern (or any phylotranscriptomics pattern) does not follow an reverse hourglass like shape. A p-value < 0.05 indicates that the corresponding phylotranscriptomics pattern does indeed follow a reverse hourglass (low-high-low) shape.

To build the test statistic again we start with a standard PhyloExpressionSet.

  Phylostratum      GeneID   Zygote Quadrant Globular     Heart  Torpedo      Bent    Mature
1            1 at1g01040.2 2173.635 1911.200 1152.555 1291.4224 1000.253  962.9772 1696.4274
2            1 at1g01050.1 1501.014 1817.309 1665.309 1564.7612 1496.321 1114.6435 1071.6555
3            1 at1g01070.1 1212.793 1233.002  939.200  929.6195  864.218  877.2060  894.8189

And again compute the TAI() profile of the PhyloExpressionSetExample.

# TAI profile of correctly assigned Phylostrata
TAI(PhyloExpressionSetExample) 

  Zygote Quadrant Globular    Heart  Torpedo     Bent   Mature 
3.229942 3.225614 3.107135 3.116693 3.073993 3.176511 3.390334 

Visualization:

# visualize the TAI profile of correctly assigned Phylostrata
PlotSignature( ExpressionSet = PhyloExpressionSetExample, 
               p.value       = FALSE ) 

The Reverse Hourglass Test is a permutation test based on the following test statistic.

1. A set of developmental stages is partitioned into three modules - early, mid, and late - based on prior biological knowledge (see Drost et al., 2015 for details).

2. The mean TAI or TDI value for each of the three modules \(T_{early}\), \(T_{mid}\), and \(T_{late}\) are computed.

3. The two differences D1 = \(T_{mid}\) - \(T_{early}\) and D2 = \(T_{mid}\) - \(T_{late}\) are calculated.

4. The minimum \(D_{min}\) of D1 and D2 is computed as final test statistic of the Reverse Hourglass Test.

In order to determine the statistical significance of an observed minimum difference \(D_{min}\) the following permutation test was performed. Based on the bootMatrix() \(D_{min}\) is calculated from each of the permuted TAI or TDI profiles, approximated by a Gaussian distribution with method of moments estimated parameters returned by fitdistrplus::fitdist(), and the corresponding p-value is computed by pnorm given the estimated parameters of the Gaussian distribution. The goodness of fit for the random vector \(D_{min}\) is statistically quantified by a Lilliefors (Kolmogorov-Smirnov) test for normality.

To perform the Reverse Hourglass Test you can use the ReverseHourglassTest() function. Using this function you need to divide the given phylotranscriptomic pattern into three developmental modules:

• early module
• mid module
• late module

This can be done using the modules argument: module = list(early = 1:2, mid = 3:5, late = 6:7). In this example (PhyloExpressionSetExample) we divide the corresponding developmental process into the three modules:

• early module: Stages 1 - 2 = Zygote and Quadrant
• mid module: Stages 3 - 5 = Globular, Heart, and Torpedo
• late module: Stages 6 - 7 = Bent and Mature

# Perform the Reverse Hourglass Test
ReverseHourglassTest( ExpressionSet = PhyloExpressionSetExample,
                        modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                        lillie.test   = TRUE ) 

$p.value
[1] 1

$std.dev
[1] 0.05598325 0.05469016 0.05386737 0.05248817 0.05161525 0.05411684 0.05605765

$lillie.test
[1] TRUE

The corresponding output shows the p-value returned by the Reductive Hourglass Test, the standard deviation of randomly permuted TAI profiles returned by bootMatrix() (apply(bootMatrix(PhyloExpressionSetExample) , 2 , sd)) and in case the argument lillie.test = TRUE, a logical value representing the goodness of fit statistic returned by the Lilliefors (Kolmogorov-Smirnov) test for normality. In case lillie.test is TRUE the corresponding Lilliefors (Kolmogorov-Smirnov) test passed the goodness of fit criterion. In case lillie.test is FALSE the corresponding goodness of fit by a normal distribution is not statistically significant.

Analogous to the plotHistogram argument that is present in the FlatLineTest() function, the ReductiveHourglassTest() function also takes an argument plotHistogram. When plotHistogram = TRUE, the ReductiveHourglassTest() function returns a multi-plot showing:

• A Cullen and Frey skewness-kurtosis plot. This plot illustrates which distributions seem plausible to fit the resulting permutation vector \(D_{min}\). Here a normal distribution seems most plausible.

• A histogram of \(D_{min}\) combined with the density plot is visualized. \(D_{min}\) is then fitted by a normal distribution. The corresponding parameters are estimated by moment matching estimation.

• A plot showing the p-values for N independent runs to verify that a specific p-value is biased by a specific permutation order.

• A bar plot showing the number of cases in which the underlying goodness of fit (returned by Lilliefors (Kolmogorov-Smirnov) test for normality) has shown to be significant (TRUE) or not significant (FALSE). This allows to quantify the permutation bias and their implications on the goodness of fit.

# perform the Reverse Hourglass Test and plot the test statistic
ReverseHourglassTest( ExpressionSet = PhyloExpressionSetExample,
                        modules       = list(early = 1:2, mid = 3:5, late = 6:7),
                        plotHistogram = TRUE, 
                        lillie.test   = TRUE ) 

The corresponding output shows the summary statistics of the fitted normal distribution as well as the p-value, standard deviation, and Lilliefors (Kolmogorov-Smirnov) test result.

This example output nicely illustrates that although the Lilliefors (Kolmogorov-Smirnov) test for normality is violated for some permutations, the Cullen and Frey graph shows that there is no better approximation than a normal distribution (which is also supported visually by investigating the fitted frequency distribution). The corresponding p-value returned by ReverseHourglassTest() is significant and illustrates that the observed phylotranscriptomic pattern of PhyloExpressionSetExample does follow the Hourglass Model assumption.

log2 transformation (TAI)

data(PhyloExpressionSetExample)
# plotting the TAI using log2 transformed expression levels
# and performing the Flat Line Test to obtain the p-value
PlotSignature( ExpressionSet = tf(PhyloExpressionSetExample, log2),
               TestStatistic = "FlatLineTest",
               xlab          = "Ontogeny", 
               ylab          = "TAI" )

sqrt transformation (TAI)

data(PhyloExpressionSetExample)
# plotting the TAI using sqrt transformed expression levels
# and performing the Flat Line Test to obtain the p-value
PlotSignature( ExpressionSet = tf(PhyloExpressionSetExample, sqrt),
               TestStatistic = "FlatLineTest",
               xlab          = "Ontogeny", 
               ylab          = "TAI" )

For the PhyloExpressionSetExample all transformations result in a significant phylotranscriptomics pattern deviating from a flat line.

Nevertheless, it is not clear which transformation is the most appropriate one since the original TAI and TDI measure were defined for absolute expression levels.

The same accounts for TDI profiles:

log2 transformation (TDI)

data(DivergenceExpressionSetExample)
# plotting the TDI using log2 transformed expression levels
# and performing the Flat Line Test to obtain the p-value
PlotSignature( ExpressionSet = tf(DivergenceExpressionSetExample, log2),
               TestStatistic = "FlatLineTest",
               xlab          = "Ontogeny", 
               ylab          = "TDI" )

sqrt transformation (TDI)

data(DivergenceExpressionSetExample)
# plotting the TDI using sqrt transformed expression levels
# and performing the Flat Line Test to obtain the p-value
PlotSignature( ExpressionSet = tf(DivergenceExpressionSetExample, sqrt),
               TestStatistic = "FlatLineTest",
               xlab          = "Ontogeny", 
               ylab          = "TDI" )

As a result, observed patterns should always be quantified using statistical tests (for ex. FlatLineTest(), ReductiveHourglassTest(), and EarlyConservationTest()). In case the observed pattern is significant, qualitative differences of the observed patterns based on different data transformations must be investigated in more detail, since most data transformations are known to cause different effects on a measure that isn’t robust against data transformations.