This was very helpull. Its been days since I was trying to understand the mechanism of this. Thank you!
@tolga1292
Жыл бұрын
Wonderful! Could you talk about STAR in your next video?
@tolga1292
Жыл бұрын
In addition with Post-alignment-QC would be wonderful :)
@AndazeBayan1
Жыл бұрын
Just like your name, your work's khusbu is reaching to those who need it the most ❤ Keep doing this great work.
@hridayhomechowdhury2142
Жыл бұрын
Thank you very much, I learned a lot from your tutorials.
@MarwaTawfikBadawy
Жыл бұрын
Thanks a million, Khushbu! Kindly keep creating these videos and go ahead for the IGV video please!
@sjwu571
3 ай бұрын
Hi loved your videos. Just want to point out, at 6:28, I think your labeling for Gene 1 is wrong. Please double check I'm not crazy. Thanks!
@lucasfleitasibarrola2322
2 ай бұрын
Yes I also noticed that!
@reinhardgrausenburger4095
Жыл бұрын
Great Video! It would be great if you could also show us how to check strandness in IGV. Thanks a lot!
@ThaoNguyen-sv2rg
Жыл бұрын
Great video Khushbu ! 6:14 Based on your explanation, for mRNA1, the antisense should be 3'5' and sense should be 5'3'. Do I misunderstand or is it the slide misrepresentation ? Thank you
@gadhakleons
9 ай бұрын
I had the same question.. Were you able to clear that?
@apostolosevgeniospavlos320
Жыл бұрын
Perfect presentation for someone who want to understand the differences between stranded and unstranded protocols. I have one question, how it is possible to understand the strandedness from GeneCounts option coming from STAR. In case of unstranded data it is clear that you ll choose the first column, but in case of stranded data how can you determine which column you choose between 2nd and 3rd?
@hinasultana2066
5 ай бұрын
Very nice presentation. I have a question. In stranded RNASeq, after the second strand cDNA is synthesized with dUTP, it is degraded. I am confused as to how the second strand information is generated later on , when that strand was degraded?
@MF-fk4lp
Жыл бұрын
Would you be able to do a tutorial on pathway analysis for individual clusters in Seurat? GSEA, GO, KEGG, Reactome, ... any of these would be great.
@chatomics
Жыл бұрын
I made a video on it recently kzitem.info/news/bejne/qoF5qoV7qad7d3Y
@perthteluguchronicles
Жыл бұрын
Thank you very much, I learned a lot from your tutorials. Can you make a tutorial on aberrant splicing events using FRAZER please
@tushardhyani3931
Жыл бұрын
Thank you ma'am !!
@aayushividhoy5943
Жыл бұрын
Hi your videos are soo good am currently preparing for a job in bioinformatics...if possible can you please guide us like what kind if questions will be asked and how we should prepare for an interview
@divyaagrawal6740
Жыл бұрын
Thank you for the video Khushbu :)
@kasmikaborah
Жыл бұрын
For biomarker identification which should I used like unstranded,stranded, reverse stranded
@hayabusa8319
Жыл бұрын
Please go ahead with IGV video...🤘
@naveennaveenkumar7127
Жыл бұрын
can u provide me your mail id I wanna talk with u mam regarding to r programming launage
@Bioinformagician
Жыл бұрын
You can find my contact information linked in the description section of every video
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