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Understanding is made easy. Thank you

Thanks prof. Please I need your help to get genotypic correlation with MET alpha lattice design. thanks

Thanks Prof. What FA stands for in the results?

Sir how i do this analysis with adjusted mean data of augmented block design please help

I have 3 environments adjusted mean data of augmented blockdesign i want to do Ammi and MTSI analysis Please help me

Hi Wakjira I am Mohamed originally from Ethiopia, studying UG MATHS AND STATS, at university of Edinburgh. can I speak to you by email please. I need help with PCA analysis in R for my project. Appreciate your help. I hope to talk to you soon

የገዢዎች ስልክ ወይመ ኢኢሜል ካላችሁ

Genotype MTSI <chr> <dbl> 1 G821 1.36 2 G183 1.36 3 G359 1.37 4 G346 1.39 5 G674 1.50 6 G686 1.53 7 G198 1.57 8 G615 1.58 9 G85 1.61 10 G251 1.64 # ℹ 269 more rows # ℹ Use `print(n = ...)` to see more rows . Thanks Prof. Please how to use this function? thanks I want to see all the MTSI results

Super amazing..

Where is the code

In the graph, we showed that the lettering (a) started from the lowest mean value, but I want to make it from the highest value. Could you help with this?

good job. but I follow this procedure and I did not know what is wrong that, I am not successful. Can you help me what the problem behind? I can send the procedures I follow if you are willing. thank you

Thank you! it's help full.would you show me how to generate this result using table.

Sir i getting error in intializeptr how i rectify the error , pls reply me sir

very clear explanations thank u

split split in rcbd over locations and years? simple latticw design over locations and years?

It looks cool, thank you:) As a beginner I have to install packages before being able to plot the heatmap: install.packages("broom.helpers") install.packages("ggstats") install.packages("GGally") install.packages("metan")

Do we need to scale our data before performing this?

Hi, great script! I'm having an issue at the step: # extracting the cld and adding to the Tk table CLD2 <- data.frame(letters=CLD$ var:n $Letters) (your GY ~ genotype : IRR, data = AKU is my yield_ha ~ var: n, data = Data) and I'm getting the error: > CLD2 <- data.frame(letters=CLD$ var:n $Letters) Error in n$Letters : object of type 'closure' is not subsettable can you help me fixing it, please? thanks E

thank u for your tutorial, keep in touch,

sometimes you have combined data that has other factors that need to appear in SOV like season, location etc

Can you explain why it is necessary to transform or standardize data? And what it is the differences?

It's very important. Would you teach us by uploading the video on how to do AMMI & GGE by plot models using linear mixed model please? I was try to handle these models using ammistability function, but some variances such as; percent of variances and commulative variances could not generate.

Dear Wakjira , i have a warming thanks and appreciation for your kindeness to deliver us this comprehensive statistical technique work. previously before follwing you in this channel i was very confused by thinking how i will analysis my thesis data and became hopeless as soon as , but now Thanks for you, i am analysizing my data using R soft ware by following each and every video you have been posting . may the God adds you more and more creative knowledge .

OVER LOCATION AND YEARS?

HELO , CAN YOU HELP ME

Dear Dr Tesfahun would make vedio for Analysis of Alphal Lattice design with mis plot using R please? With Regards,

Can you please explain why did you use Management here in ECO$Management?

Sir, here on this video the Dependent is a categorical class & the Independent are numerical. Sir, how can we develop this model for numerical Dependent as well as numerical Independent variables.

God job.

BEST 1

In addition, Whenever you need a pkg thats not on CRAN and you dont know the path, go to google and type: Pkg_name site:github.coom The first google output of This search term will most likely be a github page containing your pkg in the format: Pkg_owner/pkg_name Copy that to your install_github in prof's tutorial like this : install_github("Pkg_owner/pkg_name") Now, youre basically telling R, use GitHub to install from this github path i found online.

Sir, from the output which information I should put on my thesis.

Sir, I am facing a problem. In the console error is add = Jitter

How can i run a one way ANOVA on 6 treatments; 3 replicates per treatment with data collected at 13 time points? (I.e. 6 light treatments; 3 plants per treatment, height measured at 13 time points and i want to run ANOVA to compare treatments to control)

can you please tell me why am I having subscript out of bound error after cld step???

How to get scatterplot

Dear Dr Wakjra, I have quesion regarding when I was computing LSD.test in CRD anova I couldn't get consol function and it says error. How can I solve this ?

Good

Plz share code for generating scatter plot

A short tutorial vedio but so impactful. Thanks

I just copy and pest this code for MGIDI index?

Thank you Sir!!

You are not supposed to use so-called P values for model selection. You should be using AIC or BIC to compare models. (The P values are questionable for mixed effects models hence they are not computed by lmer.

Hello sir, How can i draw full that contain pie on down wards and number on upwards

If the number of row is large, for example my data has 140 row so what I shall do?

thans for intersting vedios bro, how can put the specific vaalue of LSD below graph with cv, P-value

So is negative degrees of freedom bad? Because it seems weird, but I see you also get it. I know it's because the two columns in the dataframe or two time-series are the same length. Even if you do order = 1, you get -1 degrees of freedom for example. Do people ever like exclude the first observations of one time series and keep the other the same to not get negative degrees of freedom??

Does R software free access?

it is good english thank you