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very useful thank you very much

no hablo espanol

I will follow you forever!

Your lecturing is so exciting and exceptional !.Dr

Omg, finally in English!!! Thank you so much - your content is invaluable!!!

thank you Dr

Thanks!

excellent

wonderful💯

Thank you 🙏 very beneficial

Very good explanation.. Thank you so much

at 2:36 from where you have copied the link? kindly reply

bioinfo is overrated, lots of tools become obsolete,.

Extremely helpful, thank you, this is exactly what I need for my final project in social networks masters class and Bio info

can you explain how to use snpEff to annotate vcf file of e.coli k12

Thank you for the video

Hello thank you for the excellent video but how can we trim the bad-quality data? Do you have any videos or article?

Here you know in which gene to look for a causative mutation. It's much harder if you don't know the causative gene.

Hello, do you know the best tool for generating VCF files from multiple sequences at once?

So well done, thank you

really clear lecture

Thank

Very nice bro, thank you so much.

Exceptional! Very focused and practical!

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!

very clear! nice vedio

Concise! Brilliant

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?

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

116 hours to evolve the Mona Lisa.

Anyone else here hopeless after the coursera project? Lol

How do you use galaxy to convert a fasta file to a tab delimited file ?

Very clear explanation. Thank you very much

This was a great video! Could you please provide any references? It would help me greatly with my final year literature review. Thanks!

From a multisample vcf file how can get only a subset heterozygous (1/2) using VCFfilter?

This helped me a lot

better than my teacher !

Great presentation. . .easy to understand and follow

good skills in delivering lectures

Very good explication!!!!Thank you very much!!!!the best

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

Thank you

Just ended the edx course. Really hyped for your next project

Very good online tutorial on genetic algorithm implementation. I love your teaching style.