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.
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@khansaiqbal79453 жыл бұрын
This is simply exceptional.
@janeckagenomics27193 жыл бұрын
Thanks!
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@karenched3 жыл бұрын
Thank you for this Sir.
@janeckagenomics27193 жыл бұрын
Very welcome
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@viviannwokorogu7140 Жыл бұрын
Thanks you so much for this insightful video. Please how can I hide the bootstrap values less than 70 as reported in many publications.
@BEINGCURIOU663 жыл бұрын
Thank you so much Sir. from India
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@anastasiyav4305 Жыл бұрын
Why do I have a small part of what should be displayed in Analysis Preferences (NJ/UPGMA)?
@shilpinagpal17383 жыл бұрын
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?
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@erisahabudin45082 жыл бұрын
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?
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@niharikadutta6323 жыл бұрын
Thank u so much
@janeckagenomics27193 жыл бұрын
Very welcome
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@sizablecracker12872 жыл бұрын
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?
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@erisahabudin45082 жыл бұрын
if the value in the phylogenetic tree is very low. what we can do?
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@SufyanKhan-qv4js2 жыл бұрын
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?
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@tanzeemazeeza.s95893 жыл бұрын
Could please explain how to interpret phylogenetic tree
@janeckagenomics27193 жыл бұрын
Sure, thanks for the suggestion. I will make a video on that and post it in the next couple weeks.
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc
@aaaa5nfgfghf3 жыл бұрын
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?
@BEINGCURIOU663 жыл бұрын
Select the seq1 and paste the seqs that you copy from notes then go to alignment and perform clustalW you will get mSa
@aaaa5nfgfghf3 жыл бұрын
@@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.
@BEINGCURIOU663 жыл бұрын
@@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.
@aaaa5nfgfghf3 жыл бұрын
@@BEINGCURIOU66 I had done the same,but the issue remain same...
@BEINGCURIOU663 жыл бұрын
@@aaaa5nfgfghf ohhh
@salihasalematia84953 жыл бұрын
hello sir, caN you give me your email, I'hVE SOME ISSUE WITH MY PARSIMONY TREE
@DrZahidMumtaz2 жыл бұрын
You will also like this method for phylogenetic tree preparation. kzbin.info/www/bejne/r5nNh6ehip2lfLc