Most useful channel for single cell RNA seq. Thank you so much for excellent explanation. Please make videos on building neural network models for single cell RNA seq data.
Your videos are just awesome! I am looking forward to the cell type identification video. Without cell type identification, all the painstaking previous steps do not have much meaning, I guess.
Thanks a lot. I've been following your tutorial for the last 8/9 months. It helped a lot with my M.S thesis and my bioinformatics Knowledge. I appreciate your time and would like to request you that it would be helpful if you make a tutorial for Cell-cell communications for scRNAseq data analysis in R.
Thanks for the video! It is very helpful, I'm looking forward to seeing a video explaining the steps of performing GO enrichment analysis, appreciate your hard work!!
New commands learn today, q10. It would be great if you show some datasets on the mouse model. Due to the lack of mouse atlas, it is a long road to annotate the cells. I believe that you will find something easy for us to do. I will be waiting for the pipeline. Thanks again! Great video as always!
Thank for these tutorials :-) I wish I had them earlier! Thanks also for including when you have errors as it is helpful for learning how to troubleshoot.
Thanks for your informative video! I have a question. Your last video had mentioned that the batch correction method 'harmony' would not change the original expression data (included 'count' or 'data' in seurat data), but add a dimensionality reduction data. However, when we use the 'FindAllMarkers' to identify the different expression genes bewteen the 'STIM' and 'CTRL', this function will use the 'count' or 'data' in our seurat data. Dose it mean we actually compared the expression bewteen 'STIM' and 'CTRL' arcoss the data without batch correction?
Great question! No matter which integration method you use, the one which returns a corrected expression matrix or the one which do not (like Harmony), we always perform differential expression test on 'unintegrated' data. That is the reason we make sure our default assay is set to 'RNA' (the assay that stores unintegrated data) prior to performing this analysis. The integration procedure inherently introduces dependencies between data points. This violates the assumptions of the statistical tests used for differential expression. So the 'count' or 'data' slot is from RNA assay that stores unintegrated data.
Lovely video! Many thanks. Do you prefer using the DEseq2 option as test.use instead of the default in the DEG analysis? Is edgeR also compatible with Seurat? Sorry, I am new to this
Your videos are super helpful and informative! Could you make a tutorial for how to integrate and analyze single-cell ATAC-seq and RNA-seq data? Thank you!!!!
Great video, thank you so much for doing it! Sorry if I missed something but I didn't finish understanding why you choose to use FindConservedMarkers() to find markers differentially expressed between one clusters and all the others. As far as I knew, this is accomplished with FindAllMarkers() and FindConservedMarkers() will give you the markers that are conserved between two groups. Maybe the reason will be that you are calculating the differentially expressed markers from one cluster versus the other groups, but with similar expressions between the two conditions (treated and untreated)?. If this is the reason, you are not supposed to have the same result using FindAllMarkers()? Thanks again and hope you can help me :)
0:18: 🔍 The video discusses finding differentially expressed features and cluster identification in single cell RNA seq data using the seurat package. 4:34: 🧬 The video discusses identifying gene expression changes in samples treated with interferon beta and the control group in a particular cell type. 9:59: ⚙ The video discusses the parameters for testing genes in clusters and populations. 14:35: 🔍 The video discusses the process of identifying cell clusters based on gene expression and grouping variables. 19:23: 📊 The video explains how to use quantiles to divide data and rename cell identities in a biological dataset. 24:20: ⚙ The video demonstrates how to perform cluster identification and find differential gene expression using pre-annotated cell data. 29:14: 🔬 The presentation discusses comparing gene expression in cd16 monocyte cells between stimulated and control groups. Recapped using Tammy AI
Thanks for the amazing tutorials! One question: how do I perform this exact analysis starting from my filtered matrix.h5 files? I have two files, for two conditions, and wanted to do the same thing you did here. Thanks !
This is extremely useful. What about using the FindconservedMarkers function to separate our cells, ie high/low PD1 expression, rather than control/treatment. Is it the same method? thanks
This videos have saved me! I have three conditions: KO/WT/DBLKO. How do I do FindMarkers() on the integrated data? I can only specify ident.1 and ident.2. There is no ident.3. Any ideas???
Your tutorials make me feel like a first year grad student getting schooled by a 5th year. Nothing better than that! Thank you. Did you ever work in the Satija lab?
Hi, thank you so much for your videos and for this topic specifically. I was trying to run it myself and I came across through this error: Error in findconservedmarkers(seurat_loom, ident.1 = 3, grouping.var = "Patient") : could not find function "findconservedmarkers" So it suggested to install these packages install.packages('BiocManager') BiocManager::install('multtest') install.packages('metap') After installing these packages, the same error keeps poping. Do you have any suggestions of what I should do?
Hi, Thanks for your great videos! You mentioned during this video that you want to make a new video about using the automatic cell annotation tools. Has this already been done?
No it hasn't been done yet, however it is very much on my list of videos to make, and hopefully I should be able to create one soon. Thanks for following up!
Great presentation. simple, clear and to the point. Application and interpretation of many functions in Seurat package are now clear to me. Just wondering did you make any video how the processed dataset: ifnb_harmony.rds was constructed using the source data? This is just to appreciate the R codes better for my own understanding as I am relatively new in this space. Thank you.
Nice content. Really helps me start from the beginning. Thank you! May I ask that how to fetch the relative expression of given genes of each animals/ conditions?
GSEA gives you an idea on what pathways are differentially enriched. It could be after you identify markers for each cluster if you are trying to understand the biological mechanism of certain cells or it could be used to help you with cluster identification. If it is latter, then it would be used after you cluster your cells. So really depends on what your goal is.
@@Bioinformagician Thank you for your response! So does this mean that you can use GSEA to find enriched gene sets between different clusters in the same dataset/condition? Like can you compare different cell type clusters in one graph using GSEA? I’m used to thinking about it as something that you can only utilize when you have a specific control dataset and another experimental dataset and you compare similar cell types between the two conditions. I’m really new to the field of scRNA-seq analysis so any thoughts would be super helpful :)
Hi, what is in your opinion the best test to use in the findmarkers or findallmakers function when comparing two cell populations with very different cell numbers?
Hi Bioinformagicain, I try to run FindConservedMarkers() but I got this message: Warning: Identity: 8 not present in group B. Skipping VVWarning: Identity: 8 not present in group A. Skipping NCError in marker.test[[i]] : subscript out of bounds. This error appears in many clusters I chose. Would you have a suggestion to troubleshoot this error? Thank you so much!
@Bioinformagician ...Yes please if you have then that would be great for people who are struggling with the unbiased annotation using packages like SingleR. Thanks in advance.
Hello thx for making such informative videos plz create video on automated cell annotation using different packages in R.. this will be a great help thx
You RenameIdents() on the Idents of the seurat object and then instead of renaming the remaining, just change the ident column to the existing annotations in the seurat object. This makes it very unclear of how someone would manually change the name of each cluster.
Thank you for your video! Would you please tell me why you choose only top gene in b.interferon.response. Could we choose more genes such as top 5 genes in this list of 1273 genes?
honestly as a computational biologist who just started working in this industry, you are so awesome
Thanks a lot. I really cannot describe how great you are
Most useful channel for single cell RNA seq. Thank you so much for excellent explanation. Please make videos on building neural network models for single cell RNA seq data.
Thank you for this very detailed and informative video, can't wait for the next scRNA-seq videos!
Your videos are just awesome! I am looking forward to the cell type identification video. Without cell type identification, all the painstaking previous steps do not have much meaning, I guess.
Absolutely, working on it. Hopefully should be able to come out with it soon.
Thanks a lot. I've been following your tutorial for the last 8/9 months. It helped a lot with my M.S thesis and my bioinformatics Knowledge.
I appreciate your time and would like to request you that it would be helpful if you make a tutorial for Cell-cell communications for scRNAseq data analysis in R.
Thanks for the video! It is very helpful, I'm looking forward to seeing a video explaining the steps of performing GO enrichment analysis, appreciate your hard work!!
I shall make a video on GO enrichment analysis soon :) Thanks!
Really amazing content. I could have saved myself months if I had found this channel earlier! Keep up the good work!
New commands learn today, q10. It would be great if you show some datasets on the mouse model. Due to the lack of mouse atlas, it is a long road to annotate the cells. I believe that you will find something easy for us to do. I will be waiting for the pipeline. Thanks again! Great video as always!
I shall consider using data from mouse models for some of my upcoming single-cell videos. Thanks for the suggestion! :)
God bless you and your videos! Thanks a lot!
Thank for these tutorials :-) I wish I had them earlier! Thanks also for including when you have errors as it is helpful for learning how to troubleshoot.
Thanks for your informative video! I have a question. Your last video had mentioned that the batch correction method 'harmony' would not change the original expression data (included 'count' or 'data' in seurat data), but add a dimensionality reduction data. However, when we use the 'FindAllMarkers' to identify the different expression genes bewteen the 'STIM' and 'CTRL', this function will use the 'count' or 'data' in our seurat data. Dose it mean we actually compared the expression bewteen 'STIM' and 'CTRL' arcoss the data without batch correction?
Great question! No matter which integration method you use, the one which returns a corrected expression matrix or the one which do not (like Harmony), we always perform differential expression test on 'unintegrated' data. That is the reason we make sure our default assay is set to 'RNA' (the assay that stores unintegrated data) prior to performing this analysis.
The integration procedure inherently introduces dependencies between data points. This violates the assumptions of the statistical tests used for differential expression.
So the 'count' or 'data' slot is from RNA assay that stores unintegrated data.
Thank you! Looking forward to your next video tutorials!☺
Lovely video! Many thanks. Do you prefer using the DEseq2 option as test.use instead of the default in the DEG analysis? Is edgeR also compatible with Seurat? Sorry, I am new to this
This is extremely helpful. If i am interested to see if there’s a cell that expressed both cd163 and cd45 how do i do that?
Your videos are super helpful and informative! Could you make a tutorial for how to integrate and analyze single-cell ATAC-seq and RNA-seq data? Thank you!!!!
That’s definitely in the pipeline. Please stay tuned :)
@@Bioinformagician You are awesome 🤩!
Really helpful tutorial. Thanks for your effort!!
Great video, thank you so much for doing it! Sorry if I missed something but I didn't finish understanding why you choose to use FindConservedMarkers() to find markers differentially expressed between one clusters and all the others. As far as I knew, this is accomplished with FindAllMarkers() and FindConservedMarkers() will give you the markers that are conserved between two groups. Maybe the reason will be that you are calculating the differentially expressed markers from one cluster versus the other groups, but with similar expressions between the two conditions (treated and untreated)?. If this is the reason, you are not supposed to have the same result using FindAllMarkers()? Thanks again and hope you can help me :)
0:18: 🔍 The video discusses finding differentially expressed features and cluster identification in single cell RNA seq data using the seurat package.
4:34: 🧬 The video discusses identifying gene expression changes in samples treated with interferon beta and the control group in a particular cell type.
9:59: ⚙ The video discusses the parameters for testing genes in clusters and populations.
14:35: 🔍 The video discusses the process of identifying cell clusters based on gene expression and grouping variables.
19:23: 📊 The video explains how to use quantiles to divide data and rename cell identities in a biological dataset.
24:20: ⚙ The video demonstrates how to perform cluster identification and find differential gene expression using pre-annotated cell data.
29:14: 🔬 The presentation discusses comparing gene expression in cd16 monocyte cells between stimulated and control groups.
Recapped using Tammy AI
Thanks for the amazing tutorials!
One question: how do I perform this exact analysis starting from my filtered matrix.h5 files?
I have two files, for two conditions, and wanted to do the same thing you did here.
Thanks !
Very informativet! Thank you! Looking forward to your next video tutorials!
This is extremely useful. What about using the FindconservedMarkers function to separate our cells, ie high/low PD1 expression, rather than control/treatment. Is it the same method? thanks
Thanks for this simplified and super informative video!
This videos have saved me! I have three conditions: KO/WT/DBLKO. How do I do FindMarkers() on the integrated data? I can only specify ident.1 and ident.2. There is no ident.3. Any ideas???
One way I can think is you can make pairwise comparisons and then intersect the DE genes from both comparisons.
Your tutorials make me feel like a first year grad student getting schooled by a 5th year. Nothing better than that! Thank you. Did you ever work in the Satija lab?
THANK you very much. You are amazing 🤩🤩🤩🤩🤩🤩🤩🤩
Hi, thank you so much for your videos and for this topic specifically. I was trying to run it myself and I came across through this error:
Error in findconservedmarkers(seurat_loom, ident.1 = 3, grouping.var = "Patient") :
could not find function "findconservedmarkers"
So it suggested to install these packages
install.packages('BiocManager')
BiocManager::install('multtest')
install.packages('metap')
After installing these packages, the same error keeps poping. Do you have any suggestions of what I should do?
Did you load the libraries after installing these packages?
Hi, Thanks for your great videos! You mentioned during this video that you want to make a new video about using the automatic cell annotation tools. Has this already been done?
No it hasn't been done yet, however it is very much on my list of videos to make, and hopefully I should be able to create one soon. Thanks for following up!
Great presentation. simple, clear and to the point. Application and interpretation of many functions in Seurat package are now clear to me. Just wondering did you make any video how the processed dataset: ifnb_harmony.rds was constructed using the source data? This is just to appreciate the R codes better for my own understanding as I am relatively new in this space. Thank you.
This is the video - ua-cam.com/video/zEuqhiu341I/v-deo.html where I explain how ifnb_harmony.rds was generated.
Nice content. Really helps me start from the beginning. Thank you! May I ask that how to fetch the relative expression of given genes of each animals/ conditions?
thank you for these videos. Very helpful!!
When we have used SCT to normalize data, I assume with should use the SCT assay for FindMarkers?
Thank you for this video !!
Hi! At what stage of the analysis workflow can you utilize GSEA?
GSEA gives you an idea on what pathways are differentially enriched. It could be after you identify markers for each cluster if you are trying to understand the biological mechanism of certain cells or it could be used to help you with cluster identification. If it is latter, then it would be used after you cluster your cells. So really depends on what your goal is.
@@Bioinformagician Thank you for your response! So does this mean that you can use GSEA to find enriched gene sets between different clusters in the same dataset/condition? Like can you compare different cell type clusters in one graph using GSEA? I’m used to thinking about it as something that you can only utilize when you have a specific control dataset and another experimental dataset and you compare similar cell types between the two conditions. I’m really new to the field of scRNA-seq analysis so any thoughts would be super helpful :)
brilliant work！
Hi, what is in your opinion the best test to use in the findmarkers or findallmakers function when comparing two cell populations with very different cell numbers?
Hi Bioinformagicain,
I try to run FindConservedMarkers() but I got this message:
Warning: Identity: 8 not present in group B. Skipping VVWarning: Identity: 8 not present in group A. Skipping NCError in marker.test[[i]] : subscript out of bounds.
This error appears in many clusters I chose. Would you have a suggestion to troubleshoot this error? Thank you so much!
@Bioinformagician did you already make a video on automatic cell annotation tools (23:15)?
@Bioinformagician ...Yes please if you have then that would be great for people who are struggling with the unbiased annotation using packages like SingleR. Thanks in advance.
That's next on my list. Hopefully should be able to come up with a video soon. Please stay tuned :)
@@Bioinformagician SingleR is a mess. I just used the scType. Not that great either.
Hello thx for making such informative videos plz create video on automated cell annotation using different packages in R.. this will be a great help thx
That will hopefully be published on my channel soon. Please stay tuned :)
How to annotation other species other than mouse, like ferret?
I want to find number of cells present in each cluster? Please help me
table(seu.obj$seurat_clusters)
You RenameIdents() on the Idents of the seurat object and then instead of renaming the remaining, just change the ident column to the existing annotations in the seurat object. This makes it very unclear of how someone would manually change the name of each cluster.
What if the seurat ident has not been given?
How do you integrate and find markers for more than two conditions?
You could integrate data and follow the pseudo-bulking approach by aggregating counts for all cells to sample level.
Please talk slower
Thank you for your video! Would you please tell me why you choose only top gene in b.interferon.response. Could we choose more genes such as top 5 genes in this list of 1273 genes?