Have you encountered this following error before? Error in Read10X_h5(filename = "/filepath/atac_v1_pbmc_10k_filtered_peak_bc_matrix.h5"): Please install hdf5r to read HDF5 files I have been able to avoid hdf5r when running locally but run into this issue on a cluster. Thank you for this video and for your help!
@mehrdadnorouzi9562Күн бұрын
Hi. thanks a lot for the great content. I really appreciate if you answer my question. is it possible that I get the results in the same order that I provide the ENSMBLEs? because I wanted to convert thousands of Ensembles to gene symbols and the I realized that the results are not in the same order. I have done DESEQ2 and at the end need to get the names of significant genes with all the other infos together. thanks again
@ashashritha214Күн бұрын
Hi mam i have completed my 12th in pcb. Is btech bioinformatics a good career option to get into this field?
@DoctorLoganPhD2 күн бұрын
Thank you for this video. How can I perform this kind of analysis on several datasets at once, to boost the number of samples being analyzed? For example, in this video, there were 4 samples in the breast cancer dataset. How would you add more breast cancer datasets to get a larger sample size and a stronger P value? Thank you!
@lukaschumchal77972 күн бұрын
Amazing video. Do you think that if I have data from gene panel in hg38, but don't know the patch, I should only cross-refer with database or try to update the data with newest assembly?
@emmayoung3303 күн бұрын
I was just trying to use lift over the other day. Great tutorial!
@marmiumiu3 күн бұрын
hi, thank you so much for the video!
@Rita-t1e5 күн бұрын
Is there any way, i can get an hour tutorial? I am Dr. Rita Bhui working as data scientist, needs some guidance on one of my project. I am stuck at calculating FPKM values after a proper alignment. I would be happy to pay you for your time.
@mahshidpooladvand85026 күн бұрын
This was the best tutorial I could possibly find online!!! You are incredibly smart! Thanks!
@Sumit5166 күн бұрын
Can this pipeline be used for variant calling in bacterial genomes? Bacterial genome is haploid as opposed to eukaryotes
@sriyellampally26498 күн бұрын
can you make a video on GeoMx bulk RNA seq analysis workflow
@PranavKatragadda-w4r9 күн бұрын
this is so good, i was paralyzed and stood up to turn it up
@cr7wakk89 күн бұрын
many many thanks to your video and it helps me a looooottt!! however there was an error when i was reading h5ad data like this : Convert("GSE246613_combined_RTPDv4_scvi_celltypist.h5ad", dest = "h5seurat", overwrite = TRUE) seurat_anndata <- LoadH5Seurat("GSE246613_combined_RTPDv4_scvi_celltypist.h5seurat") Validating h5Seurat file Error: Ambiguous assays. Is it because of the package version difference?
@nandinipatel43499 күн бұрын
Hi Khushbu, this video was really helpful and when I tried the integration tutorial, my R ran into vector exhaustion error and then the R session quit and my MacBook kinda crashed..so I wanted to ask you that which MacBook do you use ? Do you think it’s a RAM issue cuz I’m using 8gb RAM MacBook !
@fratquintero11 күн бұрын
This is conda usage video on R but you finally use renv from RStudio. renv and conda are different tools used for managing project environments, although they serve similar purposes in terms of ensuring reproducibility and consistency of dependencies.
@lincysubi673511 күн бұрын
Excellent explanation...
@ruchigupta565512 күн бұрын
How to make a scatter plot between GS AND MM
@rabiafidan925614 күн бұрын
I wish you had shown how the scatter plot and the violin plot looked after filtering... Plateuing did not start before around 6.000 but you filtered from 2.500. Why?
@072sakibsarker714 күн бұрын
Thank you so much. I learned a lot of things from your videos.
@waffles76415 күн бұрын
You mean I actually get to say I got something done tomorrow at work?! Killer tutorial, thank you so much for this
@arezoorahimi479215 күн бұрын
Hi Thanks for your great channel! I am working on identifying B cell clusters in peritoneum. Could you please provide me gene markers to identify these subpoulations? Thanks
@maert9517 күн бұрын
This is so useful, literally saving whole days of googling and trial and errors. Thank you so much!
@nikitamaurya451817 күн бұрын
I am confused between the normalization method explained in this video and the normalization method explain in another video [Difference between RPKM/FPKM and TPM | RNA-Seq Normalization Methods | Bioinformatics 101]. Which normalization is correct?
@CynthiaFrancis-sv4rc17 күн бұрын
This was great! Thank you.
@silvereyes00017 күн бұрын
From where did she get the reference genome? She didn't mention anything about it. Anyone else knows?
@moustaphagning113918 күн бұрын
GOOD JOB THANKS
@HNIK-q9x18 күн бұрын
So helpful. Thank you!
@SinergiasHolisticas20 күн бұрын
Love it!!!!!!!!!
@alfredomontes213321 күн бұрын
Hi, I'm running your code on the same dataset as you and I bumped into an Error: vector memory exhausted (limit reached?). I'm working on a MacBook Pro 2017 with a 2.3GHz Dual-Core intel Core i5 with 8Gb of RAM. I'm assuming that either the processor or RAM simply aren't enough or could there be another issue? I'm aware that this data set is quite heavy. I see you're also woking on Mac, which one would you recommend or should I just move to a PC?
@rabiafidan925614 күн бұрын
Just to complete the tutorial, use a small dataset. For your actual analyses, especially if you will integrate multiple samples/datasets, you will probably need access to an HPC.
@rezaamirahmadi601322 күн бұрын
Thanks a lots, if you have two file SRR15852371_1.fastq and SRR15852371_2.fastq ( that you teached in other your video) , what are you doing ?
@vetlove405622 күн бұрын
How did you take that geneids to the serial number ?? Please guide mee
@HominidPetro23 күн бұрын
In case 1, you said DESeq2 fits the count data to a linear model. Did you mean a negative binomial model?
@suspect_device8819 күн бұрын
The model that is fit to the counts data is a negative binomial generalised linear model which is still a linear model.
@abuhurairah499423 күн бұрын
Thank you, I am truly passionate about your mission in bioinformatics.
@Bio_infoverse24 күн бұрын
Thank you for this video. Can you please make a video on how to post projects in GitHub? Thank you
@ranamasud89724 күн бұрын
Nc
@a.k.nikson398724 күн бұрын
Awesome !
@a.k.nikson398724 күн бұрын
Great !
@qwerty1111112224 күн бұрын
0:10 what is this molecule? CH3OF?
@lanternofthegreen24 күн бұрын
I always do "a + b + a:b" and pick the results I want from it. Trying to work with a+b or a:b alone confuses me.
@qwerty1111112224 күн бұрын
As you should usually, unless a:b is very small and not significant, then just use a+b. Simpler equations are subjectively better. You can use "a*b" as shorthand for "a + b + a:b". It makes it a lot shorter when you have an experiment like "a*b*c", short for "a+b+c+a:b+a:c+b:c+a:b:c"
@lanternofthegreen24 күн бұрын
@@qwerty11111122 Damn I didn't know that. Thanks a lot!
@Spirrie200224 күн бұрын
Some of the best teaching content on KZfaq! Thank you so much and well done! 😊
@lexieoppong294624 күн бұрын
Thank you for this video! Very helpful! I have a question, if you do not mind. What would the design look like if you are controlling for multiple treatments? Would it be something like this: design = ~treatment1+treatment2+treatment3+genotype
@lanternofthegreen24 күн бұрын
Yes, but put "genotype" at the beginning. And also if you are interested in interaction terms, it would be: design = ~ genotype + treatment1 + treatment2 + treatment3 + genotype:treatment1 + genotype:treatment2 + genotype:treatment3 If you are applying each treatment separately though, meaning that your design matrix looks something like this: genotype treatment sample1 I NONE sample2 II treatment1 sample3 I treatment2 sample4 II treatment3 then you just do genotype+treatment+genotype:treatment as shown in the video.
@amirtemer72124 күн бұрын
I have to put your channel in my CV 😂. Thank you so much ^^
@BUY_YOUTUB_VIEWS_227324 күн бұрын
Mind-blowing stuff!
@mayconmarcao455424 күн бұрын
Very interesting and important topic. deseq2 is really powerful but requires different levels of understanding to be used properly. What do you mean by “doesn’t affect the fit” ? In case of a DE analysis can the DEGs be different depending the order we specify the factors in the design matrix? - not even talking about interaction terms Thanks !
@SamipSapkota-zg8hy25 күн бұрын
the value of strain samples and cell.type becomes null
@ayaqz314425 күн бұрын
thank you
@ayaqz314426 күн бұрын
thanks
@melinaguillon244928 күн бұрын
Hello :) I got an error message in my terminal when I try to unzip the file : gunzip: can't stat: GSE183947_fpkm.csv.gz (GSE183947_fpkm.csv.gz.gz): No such file or directory as well as "/Desktop/Demo/ zsh: permission denied"
@melinaguillon244928 күн бұрын
Hi! I can't install GEOquery, I get this error message: Warning in install.packages : package ‘GEOquery’ is not available for this version of R
@faezedarbaniyan178729 күн бұрын
Thank you so much for elaborating this. I can't relate the definition of Allele Frequency that you mentioned here for rows 2 and 3 in your sample (at 23:44 minutes). Can you please explain it for those?