Genomics and Biomedical Informatics
2:22
Пікірлер
@kevinshi7168
@kevinshi7168 4 ай бұрын
no hablo espanol
@SamuelAru-k5h
@SamuelAru-k5h 7 ай бұрын
I will follow you forever!
@SamuelAru-k5h
@SamuelAru-k5h 7 ай бұрын
Your lecturing is so exciting and exceptional !.Dr
@janeslt
@janeslt 8 ай бұрын
Omg, finally in English!!! Thank you so much - your content is invaluable!!!
@gazwanasadi7437
@gazwanasadi7437 8 ай бұрын
thank you Dr
@danhatechav
@danhatechav Жыл бұрын
Thanks!
@mostafamohsenidvm
@mostafamohsenidvm Жыл бұрын
excellent
@hlatywayotinotenda3895
@hlatywayotinotenda3895 Жыл бұрын
wonderful💯
@taharyasmine5944
@taharyasmine5944 Жыл бұрын
Thank you 🙏 very beneficial
@magrimeryam
@magrimeryam Жыл бұрын
Very good explanation.. Thank you so much
@gargikumari4816
@gargikumari4816 Жыл бұрын
at 2:36 from where you have copied the link? kindly reply
@AyrodsGamgam
@AyrodsGamgam Жыл бұрын
bioinfo is overrated, lots of tools become obsolete,.
@SmoothJazzin
@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
@harshitpardhi4541 Жыл бұрын
can you explain how to use snpEff to annotate vcf file of e.coli k12
@nishantpatel5085
@nishantpatel5085 Жыл бұрын
Thank you for the video
@uguremre3287
@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
@ahenk94 Жыл бұрын
Merhaba, bu sorunuzun cevabını bulabildiniz mi?
@mgold9999
@mgold9999 2 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.
@ifyifemanima3972
@ifyifemanima3972 2 жыл бұрын
Hello, do you know the best tool for generating VCF files from multiple sequences at once?
@BrandonNewell222
@BrandonNewell222 2 жыл бұрын
So well done, thank you
@akhilgajjala4922
@akhilgajjala4922 2 жыл бұрын
really clear lecture
@serychristianrenaud
@serychristianrenaud 2 жыл бұрын
Thank
@madhavanjn
@madhavanjn 2 жыл бұрын
Very nice bro, thank you so much.
@felipebatalini
@felipebatalini 2 жыл бұрын
Exceptional! Very focused and practical!
@elenips7231
@elenips7231 2 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!
@melon8419
@melon8419 3 жыл бұрын
very clear! nice vedio
@ashamerin
@ashamerin 3 жыл бұрын
Concise! Brilliant
@camilocarias5501
@camilocarias5501 3 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?
@marwanmahmoodsaleh8088
@marwanmahmoodsaleh8088 3 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
@asadrasheed1000
@asadrasheed1000 3 ай бұрын
bro can i have your contact?
@phyzix_phyzix
@phyzix_phyzix 3 жыл бұрын
116 hours to evolve the Mona Lisa.
@niusha3323
@niusha3323 3 жыл бұрын
Anyone else here hopeless after the coursera project? Lol
@yasmeenomar3639
@yasmeenomar3639 3 жыл бұрын
totally lol
@nkosinathinxumalo7643
@nkosinathinxumalo7643 3 жыл бұрын
i need assistance on that please help
@julesdrums6167
@julesdrums6167 3 жыл бұрын
How do you use galaxy to convert a fasta file to a tab delimited file ?
@JenniFadoni
@JenniFadoni 3 жыл бұрын
Very clear explanation. Thank you very much
@verafruzsinagaal3646
@verafruzsinagaal3646 3 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!
@dylandog2841
@dylandog2841 3 жыл бұрын
From a multisample vcf file how can get only a subset heterozygous (1/2) using VCFfilter?
@ernestbonatph.d.9739
@ernestbonatph.d.9739 3 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.
@joaopauloluz7793
@joaopauloluz7793 3 жыл бұрын
This helped me a lot
@protexasyt6225
@protexasyt6225 3 жыл бұрын
better than my teacher !
@jgitau001
@jgitau001 4 жыл бұрын
Great presentation. . .easy to understand and follow
@amosrechard3360
@amosrechard3360 4 жыл бұрын
good skills in delivering lectures
@melon8419
@melon8419 3 жыл бұрын
exactly!
@gisellvm3170
@gisellvm3170 4 жыл бұрын
Very good explication!!!!Thank you very much!!!!the best
@genomicsandbioinformatics9628
@genomicsandbioinformatics9628 4 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
@kusumy2620
@kusumy2620 3 жыл бұрын
hey i also want to enquire the same. please help!!
@azifahahmed4462
@azifahahmed4462 4 жыл бұрын
Thank you
@delacroidnewgen4555
@delacroidnewgen4555 4 жыл бұрын
Just ended the edx course. Really hyped for your next project
@SolvingOptimizationProblems
@SolvingOptimizationProblems 4 жыл бұрын
Very good online tutorial on genetic algorithm implementation. I love your teaching style.