Germination data and time-to-event methods: comparing germination curves

Published at July 20, 2019 ·  11 min read

Very often, seed scientists need to compare the germination behaviour of different seed populations, e.g., different plant species, or one single plant species submitted to different temperatures, light conditions, priming treatments and so on. How should such a comparison be performed? Let’s take a practical approach and start from an appropriate example: a few years ago, some collegues studied the germination behaviour for seeds of a plant species (Verbascum arcturus, BTW…), in different conditions....

Survival analysis and germination data: an overlooked connection

Published at July 2, 2019 ·  16 min read

The background Seed germination data describe the time until an event of interest occurs. In this sense, they are very similar to survival data, apart from the fact that we deal with a different (and less sad) event: germination instead of death. But, seed germination data are also similar to failure-time data, phenological data, time-to-remission data… the first point is: germination data are time-to-event data. You may wonder: what’s the matter with time-to-event data?...

Stabilising transformations: how do I present my results?

Published at June 15, 2019 ·  5 min read

ANOVA is routinely used in applied biology for data analyses, although, in some instances, the basic assumptions of normality and homoscedasticity of residuals do not hold. In those instances, most biologists would be inclined to adopt some sort of stabilising transformations (logarithm, square root, arcsin square root…), prior to ANOVA. Yes, there might be more advanced and elegant solutions, but stabilising transformations are suggested in most traditional biometry books, they are very straightforward to apply and they do not require any specific statistical software....

Genotype experiments: fitting a stability variance model with R

Published at June 6, 2019 ·  8 min read

Yield stability is a fundamental aspect for the selection of crop genotypes. The definition of stability is rather complex (see, for example, Annichiarico, 2002); in simple terms, the yield is stable when it does not change much from one environment to the other. It is an important trait, that helps farmers to maintain a good income in most years. Agronomists and plant breeders are continuosly concerned with the assessment of genotype stability; this is accomplished by planning genotype experiments, where a number of genotypes is compared on randomised complete block designs, with three to five replicates....

How do we combine errors, in biology? The delta method

Published at May 25, 2019 ·  7 min read

In a recent post I have shown that we can build linear combinations of model parameters (see here ). For example, if we have two parameter estimates, say Q and W, with standard errors respectively equal to \(\sigma_Q\) and \(\sigma_W\), we can build a linear combination as follows: \[Z = AQ + BW + C\] where A, B and C are three coefficients. The standard error for this combination can be obtained as:...

Dealing with correlation in designed field experiments: part II

Published at May 10, 2019 ·  16 min read

With field experiments, studying the correlation between the observed traits may not be an easy task. Indeed, in these experiments, subjects are not independent, but they are grouped by treatment factors (e.g., genotypes or weed control methods) or by blocking factors (e.g., blocks, plots, main-plots). I have dealt with this problem in a previous post and I gave a solution based on traditional methods of data analyses. In a recent paper, Piepho (2018) proposed a more advanced solution based on mixed models....

Dealing with correlation in designed field experiments: part I

Published at April 30, 2019 ·  7 min read

Observations are grouped When we have recorded two traits in different subjects, we can be interested in describing their joint variability, by using the Pearson’s correlation coefficient. That’s ok, altough we have to respect some basic assumptions (e.g. linearity) that have been detailed elsewhere (see here). Problems may arise when we need to test the hypothesis that the correlation coefficient is equal to 0. In this case, we need to make sure that all the couples of observations are taken on independent subjects....

How do we combine errors? The linear case

Published at April 15, 2019 ·  7 min read

In our research work, we usually fit models to experimental data. Our aim is to estimate some biologically relevant parameters, together with their standard errors. Very often, these parameters are interesting in themselves, as they represent means, differences, rates or other important descriptors. In other cases, we use those estimates to derive further indices, by way of some appropriate calculations. For example, think that we have two parameter estimates, say Q and W, with standard errors respectively equal to \(\sigma_Q\) and \(\sigma_W\): it might be relevant to calculate the amount:...

Some everyday data tasks: a few hints with R

Published at March 27, 2019 ·  8 min read

We all work with data frames and it is important that we know how we can reshape them, as necessary to meet our needs. I think that there are, at least, four routine tasks that we need to be able to accomplish: subsetting sorting casting melting Obviously, there is a wide array of possibilities; I’ll just mention a few, which I regularly use. #Subsetting the data Subsetting means selecting the records (rows) or the variables (columns) which satisfy certain criteria....

Drowning in a glass of water: variance-covariance and correlation matrices

Published at February 19, 2019 ·  3 min read

One of the easiest tasks in R is to get correlations between each pair of variables in a dataset. As an example, let’s take the first four columns in the ‘mtcars’ dataset, that is available within R. Getting the variances-covariances and the correlations is straightforward. data(mtcars) matr <- mtcars[,1:4] #Covariances cov(matr) ## mpg cyl disp hp ## mpg 36.324103 -9.172379 -633.0972 -320.7321 ## cyl -9.172379 3.189516 199.6603 101.9315 ## disp -633....