Your lecturing is so exciting and exceptional !.Dr
@janeslt8 ай бұрын
Omg, finally in English!!! Thank you so much - your content is invaluable!!!
@gazwanasadi74378 ай бұрын
thank you Dr
@danhatechav Жыл бұрын
Thanks!
@mostafamohsenidvm Жыл бұрын
excellent
@hlatywayotinotenda3895 Жыл бұрын
wonderful💯
@taharyasmine5944 Жыл бұрын
Thank you 🙏 very beneficial
@magrimeryam Жыл бұрын
Very good explanation.. Thank you so much
@gargikumari4816 Жыл бұрын
at 2:36 from where you have copied the link? kindly reply
@AyrodsGamgam Жыл бұрын
bioinfo is overrated, lots of tools become obsolete,.
@SmoothJazzin Жыл бұрын
Extremely helpful, thank you, this is exactly what I need for my final project in social networks masters class and Bio info
@harshitpardhi4541 Жыл бұрын
can you explain how to use snpEff to annotate vcf file of e.coli k12
@nishantpatel5085 Жыл бұрын
Thank you for the video
@uguremre3287 Жыл бұрын
Hello thank you for the excellent video but how can we trim the bad-quality data? Do you have any videos or article?
@ahenk94 Жыл бұрын
Merhaba, bu sorunuzun cevabını bulabildiniz mi?
@mgold99992 жыл бұрын
Here you know in which gene to look for a causative mutation. It's much harder if you don't know the causative gene.
@ifyifemanima39722 жыл бұрын
Hello, do you know the best tool for generating VCF files from multiple sequences at once?
@BrandonNewell2222 жыл бұрын
So well done, thank you
@akhilgajjala49222 жыл бұрын
really clear lecture
@serychristianrenaud2 жыл бұрын
Thank
@madhavanjn2 жыл бұрын
Very nice bro, thank you so much.
@felipebatalini2 жыл бұрын
Exceptional! Very focused and practical!
@elenips72312 жыл бұрын
Very helpful video , thank you!! I am not really familiar with bioinformatics and in this part of my project, I am trying two compare two VCF files corresponding to the results of healthy tissue and tumor tissue. I want to compare these VCF files and remove their similarities. More specific I want to remove the information of the healthy tissue from the tumor one. Have you any suggestions on which tool I should use or any way that I can do my analysis? thank you in advance!
@melon84193 жыл бұрын
very clear! nice vedio
@ashamerin3 жыл бұрын
Concise! Brilliant
@camilocarias55013 жыл бұрын
Hello, how do I determine the correct filtering threshold in VCFfilter? There is a minimum threshold value? Should I use 200 as a correct filtering threshold or can I use a 220 based on my first result?
@marwanmahmoodsaleh80883 жыл бұрын
Hello I had done the whole genome sequence by NGS (Illumina) of the bacteria. The files I received from the company are Fastaq1, Fastaq2, Filtered 1 Fastq Filtered 2 Fastq and analysis results file include :rmdup.bam.bai, rmdup.bam, filtered vcf and annotated vcf. Please tell me which of these files should be converted to FASTA and submitted to NCBI? Thanks
@asadrasheed10003 ай бұрын
bro can i have your contact?
@phyzix_phyzix3 жыл бұрын
116 hours to evolve the Mona Lisa.
@niusha33233 жыл бұрын
Anyone else here hopeless after the coursera project? Lol
@yasmeenomar36393 жыл бұрын
totally lol
@nkosinathinxumalo76433 жыл бұрын
i need assistance on that please help
@julesdrums61673 жыл бұрын
How do you use galaxy to convert a fasta file to a tab delimited file ?
@JenniFadoni3 жыл бұрын
Very clear explanation. Thank you very much
@verafruzsinagaal36463 жыл бұрын
This was a great video! Could you please provide any references? It would help me greatly with my final year literature review. Thanks!
@dylandog28413 жыл бұрын
From a multisample vcf file how can get only a subset heterozygous (1/2) using VCFfilter?
@ernestbonatph.d.97393 жыл бұрын
Thank you! Feel free to read the following blog paper on Medium website “Apply Machine Learning Algorithms for Genomics Data Classification”. This will help anyone to understand how to apply Machine Learning algorithms for genomic data classification.
@joaopauloluz77933 жыл бұрын
This helped me a lot
@protexasyt62253 жыл бұрын
better than my teacher !
@jgitau0014 жыл бұрын
Great presentation. . .easy to understand and follow
@amosrechard33604 жыл бұрын
good skills in delivering lectures
@melon84193 жыл бұрын
exactly!
@gisellvm31704 жыл бұрын
Very good explication!!!!Thank you very much!!!!the best
@genomicsandbioinformatics96284 жыл бұрын
Very informative session. Great work. Please make a tutorial on snpeff. How to customize snpeff according to our needs. I mean how can we do variant annotation on snpeff for a list of snps that we mostly get after genome wide association. Thanks
@kusumy26203 жыл бұрын
hey i also want to enquire the same. please help!!
@azifahahmed44624 жыл бұрын
Thank you
@delacroidnewgen45554 жыл бұрын
Just ended the edx course. Really hyped for your next project
@SolvingOptimizationProblems4 жыл бұрын
Very good online tutorial on genetic algorithm implementation. I love your teaching style.