really appreciate your videos🎉❤cannot wait to see spatial omics tutorial in the future😊
@sanbomics
5 ай бұрын
Right now I am eagerly waiting some interesting datasets with newer more high res technology than visium
@lly6115
5 ай бұрын
Good to see you back😊 and thank you for your update
@sanbomics
5 ай бұрын
Yeah sorry I have been busy! Shouldn't be as long between the next few videos.
@ykoy1577
5 ай бұрын
I was waiting for your video. your video is so helpful for beginner like me. Thank you so much for sharing your knowledge and experience
@babyfriedrice4878
5 ай бұрын
i love sanbomics so much!!!!!!!!!!!!!!!!!!!
@sanbomics
5 ай бұрын
I love you too!
@piroDYMSUS
5 ай бұрын
Amazing work, hope we will see second part soon
@sanbomics
5 ай бұрын
Trying to release in the next week or two!
@MrJordi94
5 ай бұрын
You trully are an inspiration for rna-seq! Love your videos and your communication skills. Hope to see the rest of the 2024 tutotial soon :D
@sanbomics
5 ай бұрын
Thank you
@caspase888
5 ай бұрын
I look forward to your videos. Your grasp on the subject and the ability to teach are amazing. Thanks a lot 👍🏻
@sanbomics
5 ай бұрын
Thank you! :)
@roberto1697
26 күн бұрын
This is amazing and I'm fully on your side about creating envs with conda, but then installing everything via pip. Such a guilty pleasure, haha!
@dardas15
5 ай бұрын
this is fantastic and really helps people with limited bioinformatics background to independently analyze data-thanks so much for making these videos, ive been using them with python ever since you shared a few years ago!
@jackmineeechen4380
5 ай бұрын
I started with the video camparing different intergration method. That one really helped me! I eventually choose scanorama for my dataset, which worked out. Looking forward to this series! I appreciate your videoes!
@avp300
5 ай бұрын
this is brilliant! can't wait for part two!! Ridge plot look awesome! thank you Mark! :-)
@sanbomics
5 ай бұрын
Tomorrow hopefully!
@taoufikbensellak9274
5 ай бұрын
I just started your sc guide and I really enjoy it. Just for some clarifications about the tools, I use mamba (conda) with python 3.8 and a lower version of pandas (
@sanbomics
3 ай бұрын
I'll be doing DE using a different approach this time which should give people fewer issues. Diffxpy can be a struggle so I don't really use it anymore
@yaseminsucu416
5 ай бұрын
You rock! Thank you for doing this, looking forward to following this series!
@jianhuacao7180
5 ай бұрын
welcome back, bro. Your channel is better than before.
@sanbomics
5 ай бұрын
Thanks! I am trying to continually improve the quality and make videos people are actually interested in.
@DuqueVJ
5 ай бұрын
Amazing! Thanks very much for the tutorial, I'm learning a lot!
@moonmoun2983
5 ай бұрын
Waiting impatiently for the next part
@sanbomics
5 ай бұрын
Wait no further! :)
@jonathanback5731
5 ай бұрын
Your work is fantastic, great content!
@alexeyryzhenkov7579
4 ай бұрын
Thank you for your work!
@sanbomics
4 ай бұрын
Thank you so much!!! Really appreciate it! :)
@laloulymounia9266
5 ай бұрын
Thx for the update !
@enkiduedmond1888
Ай бұрын
Amazing practical vedio! Just wanna ask r u still offering personalized courses? I saw it from your website and want to buy it😊
@brunovinagre427
5 ай бұрын
gratefull Mark!!
@maiduong9265
2 ай бұрын
hello, I am newbie and learning to analyse sc RNA data from smart-seq3. Please make some tutorial to help me with preprocessing. Thank you very much for your work!
@孟鹏飞-y9y
5 ай бұрын
You were great.
@islemgammoudi842
5 ай бұрын
Thanks for the Videos. Currently, I'm embarking on the journey of analyzing single-cell RNA sequencing (scRNA-seq) data combined with CITE-seq data. However, I'm facing challenges related to duplicate discrimination and assigning sub-samples via hashtags. Given your expertise in this area, I was hoping you could provide some guidance and advice on how to navigate these challenges effectively.
@fsh9134
3 ай бұрын
Thanks for making very useful videos. I was wondering if you would like to make a video related to single cell analysis using Julius AI a data analysis AI.
@kristifourie8427
5 ай бұрын
best page ever
@sanbomics
5 ай бұрын
Thank you :)
@frutitadelosmares
3 ай бұрын
Hi! Thanks so much for such a great tutorial! Have a naïve question of someone who just started in this world: When raw data is not available, for example, you can only download normalised filtered values, do you skip the pre-processing step? Is it correct to pre-process normalised values, let's say tmm? Again, thanks so much for all the videos!
@sanbomics
3 ай бұрын
Yeah if there are no raw counts then you will have to skip the ambient removal. Unfortunately, this is the only way sometimes.
@moonmoun2983
5 ай бұрын
I would like to thank you immensely because you’re one of the few bioinfo channels I can follow along, I have a question regarding a result I obtained from a following the previous full scRnA seq walkthrough you posted a year ago. I tried applying the code to a before and after chemotherapy treatment. Everything worked perfectly until i got to the deg analysis part with heat maps, With 25 top upregulated and downregulated genes and the filtering codes it didn’t yield more than 12 degs, so I had to reduce the filtering and kept genes with significant fold change above 0.05 . And I ended up with more differentially expressed genes, however in both cases my heat map was devoid of pattern, both the condition and control looked mostly downregulated. Should I conclude that there is no deg or expression signatures in both cancer sample before and aftertreatment? Because the original paper i took my data from didn’t do a deg analysis for the whole dataset but selected 4 patients out of 12 to create a deg heatmap with less than 10 genes. thank you, I’d highly appreciate your insight on my results
@sanbomics
5 ай бұрын
Its really hard to say without knowing more and actually getting a feel for the data. You can try a pseduobulk approach and see if you have and degs. I have a video on that, but will also be covering it soon in the new tutorial series.
@MinnnWang-uv8bn
5 ай бұрын
🎉🎉🎉thanks!
@asshimul1168
2 ай бұрын
Hello, Would you please make a tut on advance workflow (based on good paper) on sc RNA Seq by using R?
@hehe-k2c
6 күн бұрын
Very good tutorial, but this error is bothering me, can you help me with it, thanks a lot! ”ValueError: row index exceeds matrix dimensions“
@ncedilemankahla9758
2 ай бұрын
love your channel. quick question at the beginning when you rename the files. 's/genes/features/'* why the "s" at the beginning?
@freeweed4all
Ай бұрын
It's a common way to say "substitute". It is used also with sed, vi and in general regex patterns.
@mehdiraouine2979
5 ай бұрын
amazing work as always ! on a side note, if I were to download a fastq data from GEO with no specification of whether the adapters were removed or not in the paper, how should I check if they were removed on python.
@sanbomics
4 ай бұрын
I wouldn't use python to do it only because there are several command line tools that are much faster that can do the same thing. Like cutadapt
@DeeptiMittalArora-e7z
20 күн бұрын
Amazing video, but I am having issues with codes as I am working on windows. What would you suggest?
@cocomom1808
2 ай бұрын
thanks a lot! However, when I was using your pp function to handle the doublets, it always gave me the AttributeError: 'csr_matrix' object has no attribute 'A'. Do you have any idea of how to fix it? Thanks in advance
@CaveCrack
5 ай бұрын
Thanks for the great video and series. I have a question at around 36:40 on how to interpret the graph. If the experiment had loaded say 14000 cells it appears that around 8000 would be recovered which I assume we would interpret as the number called by cellranger... For 14000 cells loaded the multiplet rate appears to be 6%, 6% of 14000 being 840 expected multiplets. However, all the blue recovery dots are aligned around 4.5%. 4.5% of 8000 would be only 360 expected multiplets. The document from which the graph is extracted says "Generally an increased number of cells per sample will increase the doublet rate". I've not been able to find clarification. Thank you
@CaveCrack
5 ай бұрын
Also, I am wondering if your low number of detected doublets at 1e-16 was due to the previous QC step where you exclude cells with the highest logp_total_counts and log1p_n_genes_by_counts, as these could filter a lot of doublets.
@sanbomics
5 ай бұрын
I think in this case just ignore the blue line. The more cells you load the higher multiplet rate and more total multiplets you will have
@sanbomics
5 ай бұрын
Exactly, it's hard to say exactly what percent the multiplets are because of the first step. I think I mention it in the video briefly... or at least i thought it
@gerolduntergasser4000
5 ай бұрын
cool good job😁
@abellopez8017
5 ай бұрын
Hello! Thanks for the Video, I will begin my PhD in Bioinformatics in August, what computer do you have?
@sanbomics
5 ай бұрын
Well.. at home I have a 32 vCPU, 128 gb ram, rtx 4090. At werk I have a 64 cpu, 256 gb RAM, rtx 4090. Sometimes I have to use AWS when I need more than that. Depending on what you plan to do it can vary a lot.
@mehdiraouine2979
5 ай бұрын
Another question: if you were to choose between SCVi model for detecting doublets and this clf doubletdetection method, which one is more straightforward? I feel like this method needs some tinkering around depending on the specific dataset
@sanbomics
4 ай бұрын
The best method would be to use multiple methods. They will all give you slightly different results but hopefully have significant overlap. The reason I used doubletdetection here is because it is fast/simple and I already have multiple video tutorials on SOLO (scVI). It's hard to say which is more accurate. Changing parameters in scvi/SOLO will likely change the results a lot too just like what happened here.
@caspase888
3 ай бұрын
Your videos are amazing. Thanks a lot. Could I use 3050 with 64 GB RAM for this kind of analysis? Thanks a lot.
@sanbomics
3 ай бұрын
You can do a decent number of cells with 64 gb ram. I would think you could handle around ~200k in memory at the same time without too many issues. Some steps/algoirthms use a lot more memory though so it is highly dependent on what you do. In my experience 64 gb wont be enough for large datasets/atlases but you can def do small numbers of samples.
@555gong9
5 ай бұрын
Thank you for such a great video. Which is better for removing doublets, doubletdetection or the previous SCVI method?
@sanbomics
5 ай бұрын
I haven't done or seen a comparison between the two. The best would probably be to run both and see how they overlap. All i can say is that doubletdetection is easier and faster
@555gong9
5 ай бұрын
Thank you for your advice, I will try it next, thank you very much, my superhero.
@supakornpongpakdee1544
5 ай бұрын
Thank you very much for creating this tutorial! Looking forward to the next lessons!😊❤
@pinchos90
4 ай бұрын
are you're still going to develop workflows for R or you're sticking with python?
@sanbomics
4 ай бұрын
I prefer python, but even this tutorial series will have some R in it because it is unavoidable. So I will have more R videos in the future
@AP-vo7gp
5 ай бұрын
Sir, I have count matrix and want generate annotation matrix out of it then do the batch correction and then DGA plz help via process as i am not getting suitable results.
@sanbomics
3 ай бұрын
Hi it is hard for me to help without knowing more specifics and what the issue you are having is
@AP-vo7gp
3 ай бұрын
@@sanbomics thanks alot sir I was able do it :)
@goddyhong
5 ай бұрын
thx for sharing! if i use a filtered matrix for analysis, do i still need to remove the background RNA? since i dont have a 4090🤣
@sanbomics
5 ай бұрын
If you have a filtered matrix you can't remove background RNA. But if its just a time thing, you can use your CPUs with SoupX. I have another video on that. If you only have filtered counts, you are stuck with what you have!
@ghujka
4 ай бұрын
Have a beer on me bro🍺
@sanbomics
4 ай бұрын
Thank you!!! I can do that ;)
@charlieintampa6769
5 ай бұрын
F%(k. Seems super useful but you could have been speaking any random language and I would have understood about the same.
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