Hey Lana, I just used your code for counting the point mutations - resulted always in 1 independently on the amount of point mutations. But I found a way to fix it :) - Maybe also interesting for others trying to solve the problem :) def hamming_distances(s,t): if len(s) != len(t): print("Strings are not equal size!") else: hamming_dist = 0 for position in range(0, len(s)): if s[position] == t[position]: continue else: hamming_dist = hamming_dist + 1 return hamming_dist print(f"Hamming distance for this example is: {hamming_distances(s, t)}")
@LanaDominkovic2 жыл бұрын
Thank you Lisa for checking. I pinned your comment just in case anyone else get’s the same problem. Thank you so much for sharing!:)
@AliRaza-lo5tg2 жыл бұрын
actually, you are not using the same function. recheck please
@CaucherIlami Жыл бұрын
Hey Lana, Your channel is awesome. Thanks for sharing such mind catching videos. I've learned Biopython using your tutorials.
@LanaDominkovic Жыл бұрын
Glad you like them!
@CaucherIlami Жыл бұрын
You made life live! thanks for your support. May I have your email id? I have some queries about codes that you run in this tutorial@@LanaDominkovic
@danielnakamura64302 жыл бұрын
I just found your channel! You are amazing
@LanaDominkovic2 жыл бұрын
Thank you for nice words :) hopefully it will be useful to you and you will learn something new :)
@chandansaini58603 жыл бұрын
Thank you so much for this video. Keep uploading such videos
@LanaDominkovic3 жыл бұрын
Thank you so much for nice feedback. I will, I am uploading videos once per week :)
@lacapmf3 жыл бұрын
thank you, this helped me a lot!
@LanaDominkovic3 жыл бұрын
Happy to hear that! 🥰
@LanaDominkovic3 жыл бұрын
Thank you for visiting my channel! Please don’t forget to show some support by subscribing and liking the content. Let me know in the comments below what would you like to see next :)
@vincentdarbot7743 жыл бұрын
Nice video, hope you will resolve others Rosalind problems ( I'm stuck with some of them 😄 )
@LanaDominkovic3 жыл бұрын
Let me know which one you are stick with so maybe I can help! Thanks for nice feedback. I am happy that you liked it! ❤️❤️
@jessehines40447 ай бұрын
Which code editor for python do you use? Great video BTW, I loved it.
@LanaDominkovic7 ай бұрын
Hi, I use PyCharm. Thank you for your comment :D I am really glad you loved it
@jessehines40447 ай бұрын
@LanaDominkovic Of course, you're welcome your videos are great. Wow pycharm, that's expensive because for the scientific version, they charge 99$/month.
@LanaDominkovic7 ай бұрын
@@jessehines4044 you dont need professional, download community edition should be enough :) and that one is free
@sanaomar21822 жыл бұрын
to understand what you are saying I need to understand the symbols TTT and so on, and other stuffs. considering this, what so you recommend me to study first? thanks
@LanaDominkovic2 жыл бұрын
Genetic code and nucleotides :)
@shoebikhlas5784 Жыл бұрын
Hi Lana, really appriciate your efforts. You really explains it very well. I am a bigginer in this feild. I was curious, if we can count number of mutations in each individual sequence of a fasta file (fasta file having multiple sequences) and print out the result " sequence header and corresponding number of mutation detected". In one of my project i have to sort and remove sequences from my fatsa file having mutations more than a set threshold.
@LanaDominkovic Жыл бұрын
Hi, thank you for the nice comment. yes it would be possible to count number of mutation in each individual sequence, you would just need to know delimiter in file which recognises the start of new sequence and when reading file, count sequence by sequence