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DnA lab short read sequencing workshop
Приєднався 12 лип 2021
Single Cell Clustering and Cell Type Identification
This video covers clustering of single cell expression patterns and identifying cell type.
Created by: Jesse Kurland, 2024.
This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Created by: Jesse Kurland, 2024.
This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Переглядів: 162
Відео
An Introduction to Cell Chat
Переглядів 152Місяць тому
This video covers examination of cell-cell comunication in single cell sequencing. Created by: Georgia Barone, 2024. This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Single Cell Sequencing
Переглядів 750Місяць тому
This video will provide an overview of single cell sequencing. Created by: Chris Ozeroff, 2024. This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Single Cell Sequencing Analysis and Seurat
Переглядів 98Місяць тому
This video covers the basics of analyzing single cell sequencing data and the Seurat package. Created by: Jesse Kurland, 2024 This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Single cell cell-type annotations
Переглядів 1042 місяці тому
This video details the two main methods people use to get cell type annotations: mapping to a known atlas & using marker genes.
Single Cell Sequencing Analysis (Abbreviated)
Переглядів 157Рік тому
This video covers the basics of analyzing single cell sequencing data. Created by: Jesse Kurland and Chris Ozeroff, 2023 This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
R for Beginners PHD Mamas version
Переглядів 125Рік тому
This video demonstrates the use of R for people that have never coded before. I taught this class over Zoom for the Facebook group Ph.D. Mamas, because there was a large discussion about the best ways to learn R if you have never used R before. You can learn R via a book, but it's much easier after seeing this video.
Introduction to BEDTools
Переглядів 2,8 тис.2 роки тому
This video will describe the file formats, uses and usage of BEDTools. Created by: Rutendo Sigauke 2022. This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Multifactor Designs in DESeq2
Переглядів 9 тис.2 роки тому
This video will talk about advanced conditions and designs for differential expression analysis in DESeq2. Created by: Sam Hunter 2022. This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
DnA Lab Short Read Sequencing Workshop BIOTA18 7 21 2021
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DnA Lab Short Read Sequencing Workshop BIOTA18 7 21 2021
DnA Lab Short Read Sequencing Workshop BIOTA18 7 22 2021
Переглядів 1393 роки тому
DnA Lab Short Read Sequencing Workshop BIOTA18 7 22 2021
DnA Lab Short Read Sequencing Workshop BIOTA18 7 20 2021
Переглядів 1003 роки тому
DnA Lab Short Read Sequencing Workshop BIOTA18 7 20 2021
DnA Lab Short Read Sequencing Workshop BIOTA18 7 26 2021 complete video only
Переглядів 1083 роки тому
DnA Lab Short Read Sequencing Workshop BIOTA18 7 26 2021 complete video only
DnA Lab Short Read Sequencing Workshop BIOTA18 7 19 2021
Переглядів 1343 роки тому
This is the in-class recording of the short read workshop.
Visualizing sequencing data
Переглядів 8073 роки тому
Visualizing sequencing data with IGV Credit by , 2017 This video is part of the DnA Lab short read sequencing workshop run every summer in Boulder, Colorado. For more information go to dna.colorado.edu/education.html.
Isoform differential expression analysis with Ballgown
Переглядів 7733 роки тому
Isoform differential expression analysis with Ballgown
I want to love and be loved like that
Thx for the good explanation !
Thank you
This video is like a journey that I never want to end. Magnificent!
Thank you very much, it is very helpful. Can you share the complied bash script (#!/bin/bash/ for all WGS and GBS starting from fastqc, multiqc, trimmonatic, bwa, samtools, GATK(bcftool/vcftool), please? Thanks in advance.
Thank you very much for sharing! I am a biologist without any computational background, your video is very helpful to get me started using R in my research!
Thank you, this is very helpful!
How do I download and install Bowtie 2
Is day 7 where dispersion and other estimates explained uploaded anywhere? I would love to see know what is explained there.
HELP
HELP
This is a helpful and well written explanation of Bowtie2. The audio quality of this explanation, however, is incredibly poor. I had to crank up the volume to barely understand what you were saying.
Hello! Thank you for your video this topic is definitely cause for confusion. I am stuck on chapter 8 and hoping you could clarify where my thinking error is? I have an RNASeq exp with 3 time points and 3 treatment types+a control(DMSO). I run DESeq() as below twice, once using the 24hour as a reference point and once for the 48hour. I believe I should be extracting the same result below as you explain in your video (here treatment effect "Ibr" at 48 hours), but the results differ. design<-~passage+inc_time+treatment+inc_time:treatment dds1 <- DESeqDataSetFromMatrix(countData=countData, colData=colData, design=design) dds1$inc_time <- relevel(dds1$inc_time, ref = "24") dds1 <- DESeq(dds1) R1<-results(dds1,contrast=list("treatment_Ibr_vs_DMSO","inc_time48.treatmentIbr"))%>%as.data.frame() dds2 <- DESeqDataSetFromMatrix(countData=countData, colData=colData, design=design) dds2$inc_time <- relevel(dds2$inc_time, ref = "48") dds2 <- DESeq(dds2) R2<-results(dds2,name="treatment_Ibr_vs_DMSO")%>%as.data.frame() > R1[4,] baseMean log2FoldChange lfcSE stat pvalue ENSCAFG00000000007 469.7007 0.1701164 0.2742005 0.6204087 0.5349888 padj ENSCAFG00000000007 0.8295431 > R2[4,] baseMean log2FoldChange lfcSE stat pvalue ENSCAFG00000000007 469.7007 0.08185999 0.1228012 0.6666058 0.505024 padj ENSCAFG00000000007 0.7109824 Would greatly appreciate any help!
I will share your channel with my firends
thansk so much for this videos I really enjoy it and I know it is really hard to create a content on youtube without high interaction to make to income but all I can do is subscirbe and push the like button for you thanks again
Please upload more videos on variant calling you could be saving a life literarily. Thank you
can you send me script of these all commonds
hi, very well explained, thanks. question: I have a set of data which has this condition: 1. severe drought in short time 2. severe drought in long time 3. mild drought in short time 4. mild drought in long time now, I want to make a meta data but I'm not sure whether I should make one single column which contains all the conditions and their controls or I should make separate columns for short + long + severe + mild any suggestion would be appreciated.
Hey! I also have similar case. Did you find a way to design your conditions? Thanks in advance!
Tbh I want my dna short read
why dont you short read my DNA ;)
Everyone who doesn't code thinks bioinformaticians hit some magic button to spit out analysis. LOL. Super amped for this class.
Thank you so much! I was really lost with the analysis of ATAC-seq, but I feel way more confident in my essay of ATAC thanks to your video. Greetings from Chile.
it's a really hard topic lol check out this video as well ua-cam.com/video/5HfNP-VVJWU/v-deo.html
@@pancake9191 thank you! I already turned my essay, but I'll check it out anyway! ☺️
Can i trim my rawreads twice?... meaning i trim raw reads and take the results and trim them?
Hi, I would like to ask if my understanding about how the mean gene expression level is calculated in the figure on the right is corrected: Suppose that there are 5 replicates and each cover 1000 different genes. Next, we calculate the mean of expression levels for each gene over 5 replicates and show them in the X axis. For the Y axis, we calculate the variance instead of mean. Is that correct? I am a little bit concern about the word "Pooled" in the Y-axis's title. Does it has any different meaning compared to those for calculating values on the X-axis? Many thanks!
Very good presentation