Excellent Muruli Sir

Sir, how do we arrange the data in case of multiple band?? Could you please share a raw data file with multiple band arranged for analysis??

Tahnku so much

how to get path digram for gcv and pcv

Sir, can you share raw data file diversity analysis

I want buy

Thanks for your great explination sir! My humble request to you could you please make a video on the different QTL mapping softwares available till 2024 and their comparison details in a short video.Im writing my PhD thesis on QTL mapping in rice and this will be helpful for me as no proper information is available. Thanking you.

How to do analysis in factorial RBD (2 factors) (2 years)

thanku this was very helpful

what to do if they are showing that there is not enough degree of freedom during analysis?

thank you for your best teaching us and if possible for you do it on different kinds of fertilizers and soil fertility

Thank you

Virat Kohli ❤️❤️👑

Sir it isn't working on my data work. When I'm using character value 5, no. Of treatment 14, no. Of replication 3 , dependent variable 5, and independent variable 1,2,3,4 ... Not working in this way. Help to get more details on it.

The page cannot be displayed because an internal server error has occurred. now i analysis my data con"t open

Sir, what if number of treatments are not equal in each block

Thank u so much sir 😊

Sir i send you data plz check it and told me plz sir i am worried

Kiya kron mn ab

Sir meri 50 genotypes hn is k liy genotypic coreltion ka 500 errer dey rha agr mn 12 ka krti hn to results ajaty hn

Analysis p click kr ti hn to errer deta h

Sir mn kr rhi hn ni hu rha errer dey rha h

can we analyse RAPD data also through this software??

How to perform pooled analysis in factorial CRD or RBD of two years data.

2. I am facing problems to save my outputs as docx file. when i give command it shows results as ------- Error in read_xml.raw(charToRaw(enc2utf8(x)), "UTF-8", ..., as_html = as_html, : PCDATA invalid Char value 27 [9]..... and it say that ''Removed 2 rows containing missing values (`geom_segment()`). How to solve this?

first of all thank you for your nice presentation about augmented block design, saying this after analysis my data "report.augmentedRCBD.bulk(bout, file.path(tempdir(),'' is not working when I doing all analysis finally it says that,,, Error in read_xml.raw(charToRaw(enc2utf8(x)), "UTF-8", ..., as_html = as_html, : PCDATA invalid Char value 27 [9]....so how to report my data result thank you.

Sir what is that DLL error in bip I couldn't able to solve it

Sir while uploading the bip file for qtl analysis it is showing DLL name = checkerrorBIP

Sir can you explain how to arrange the data for augmented design in op stat

Very useful.... thanks a lot,sir ❣️

Hi sir, nice video. In case of phenotypic data, can we feed multiple traits simultaneously or should we feed individual traits one by one?

I have unreplicated genotypes, replicated checks, 3 Blocks and two-year data. Is it possible to add year in the script so we can have also the ANOVA results for year and interaction between geno*year, block*year? Thank you!

would you like to share this software link if it is free please?

There's no SeM mentioned in analysed data... Please help

How tp calculate GCV PCV and genetic divergence sir

Good Morning Sir Is it possible to analyze GCV, PCV , path, D sq in ABD without having replicated data

Excellent tutorial. Just one doubt, what is missing data code 99/999 ??? What does that indicate??? Let me know sir

Hi Thank you for such a nice explanation in the video. It is really helpful. But when I’m entering my data my input file is not being accepted. Can you help ?

Thank you so much sir Very helpful video

sir..please i wann this app what is the name of app

pc m nhin chal raha h

sir, i am putting datas as you told but it is showing 500 internal server error. Please sir, tell me the solution.

Thank you for your neat and clear explanation..

make a video on how to conclude the observed tables that we got after analysing our data

Sir, Which R should we install for this AUGRCBD. I am trying it with R 4.5 it saying use proper R software

SIR, VIDEOS ARE VERY HELPFUL PLEASE EXPLAIN HOW TO INTERPRETTATE THE DATA OUTOUT of OPSTAT of this portion direct and indirect effects

Hello sir, I am also conducting an experimental trial in Augmented Design. The experiment consists of 3 checks, 52 genotypes and 4 blocks so the error degree of freedom is 6. I want to ask that whether it is correct or the error df should be more than 10 compulsorily. If that so then I will need to add 2 more checks in my trial in order to make error df equal to 12.

Your explanation is simple and easy to understand. You've saved me so much time . Thank you😭🤧 i subscribed

Nice Dr. Murali... Helpful to all breeding students...

Thank you very much. In your video at time point 13:59 after selecting qic[result, if the window shows nothing, does it mean no QTL is detected?