Making a Phylogenetic Tree with Bootstrap Support Values in MEGA

[@joseantoniogutierrezbarran387]

Thank you very much for this video. I was using MEGA for a long time, and with this video I have learned a lot of interesting features.

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@khansaiqbal7945]

This is simply exceptional.

[@janeckagenomics2719]

Thanks!

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@karenched]

Thank you for this Sir.

[@janeckagenomics2719]

Very welcome

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@viviannwokorogu7140]

Thanks you so much for this insightful video. Please how can I hide the bootstrap values less than 70 as reported in many publications.

[@BEINGCURIOU66]

Thank you so much Sir. from India

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@anastasiyav4305]

Why do I have a small part of what should be displayed in Analysis Preferences (NJ/UPGMA)?

[@shilpinagpal1738]

Hi, Could you please tell me that while finding the best substitution model, what should be used at missing data for protein alignment? Also, what is the J-model test? IS this substitution model the same as the Jmodel test?

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@erisahabudin4508]

I have a problem after making a phylogenetic tree. The bustrap value is less than 50.. even only 30. how to get bootstrap value up than 70 or closed to 100?

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@niharikadutta632]

Thank u so much

[@janeckagenomics2719]

Very welcome

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@sizablecracker1287]

could you help me, when i choose the option to open find best dna/protein, the same file save as fasta doesn't show up,, what do i do?

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@erisahabudin4508]

if the value in the phylogenetic tree is very low. what we can do?

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@SufyanKhan-qv4js]

Hello, sir very informative video. Sir, can you tell me that how can we copy the MSA from MEGA X to MS Word for publication?

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@tanzeemazeeza.s9589]

Could please explain how to interpret phylogenetic tree

[@janeckagenomics2719]

Sure, thanks for the suggestion. I will make a video on that and post it in the next couple weeks.

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc

[@aaaa5nfgfghf]

Sir, I am aligning sequencing in MEGA format, but after opening the same file, I am getting message "Align Sequences must be of equal length". How to fix this problem?

[@BEINGCURIOU66]

Select the seq1 and paste the seqs that you copy from notes then go to alignment and perform clustalW you will get mSa

[@aaaa5nfgfghf]

@@BEINGCURIOU66 I am getting true result when performing MSA using clustal omega, but when performing same with MEGA X, i am getting two types of errors..one is 'Align sequences must be of equal lemgth' and another error is 'unnamed base found at line 351'. I have also checked the nucleotides in the note pad it is correct, then how the error is showing in MEGA X. please help in the same.

[@BEINGCURIOU66]

@@aaaa5nfgfghf make sure that all the seq that you have in note is partial seq anot if you have 1 genome seq. Then it creates issue u can check this also bcz i also had trouble doing this then i remove whole genome seq.

[@aaaa5nfgfghf]

@@BEINGCURIOU66 I had done the same,but the issue remain same...

[@BEINGCURIOU66]

@@aaaa5nfgfghf ohhh

[@salihasalematia8495]

hello sir, caN you give me your email, I'hVE SOME ISSUE WITH MY PARSIMONY TREE

[@DrZahidMumtaz]

You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc