DESeq2 | Differential gene expression analysis
kandi X-RAY | DESeq2 Summary
kandi X-RAY | DESeq2 Summary
Differential gene expression analysis based on the negative binomial distribution
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DESeq2 Examples and Code Snippets
Community Discussions
Trending Discussions on DESeq2
QUESTION
I'd like to generate a PCA of my bulk RNAseq data, coloured by each of my variables in the DESeq2 object "vsd". My current code looks like this (to generate a single plot):
...ANSWER
Answered 2022-Mar-09 at 18:08Let's mock up some data, since the example you provide is too short and ill-formatted to do anything with. I'm assuming you have data of roughly the following structure:
QUESTION
I have this piece of R
code that should plot some data growth_data.txt. Basically, it should plot a line graph showing a single line (or line + points) for the control and treated animals in this dataset. That is, one line for all the controls and one line for all the treated animals. Add appropriate error bars for each time point. But I don't know why the plot doesn't show the line and error bars on the plot which is weird.
What is wrong in my code? How to fix it? I included the plot I'm getting now.
...ANSWER
Answered 2021-Oct-11 at 02:50I'm sorry - I was incorrect about "Day" being a factor - thanks for fixing the broken link.
One potential solution is to add a 'group' aesthetic, e.g.
QUESTION
I have a data-set comprising of an OTU table, where rows = samples and columns = OTUs, like this:
Otus <- data.frame(OTU_1 = c(0, 0, 1), OTU_2 = c(12, 0, 5), OTU_3 = c(0, 5, 3), row.names = c("S_1", "S_2", "S_3"))
I moved it from phyloseq
over to DESeq2
using the phyloseq_to_deseq2
command without issue. Now that it's a DESeq2
object, I want to normalize the OTU table using the variance stabilizing transformation with the following command:
ANSWER
Answered 2021-Oct-08 at 05:55What is your intended purpose for the variance-stabilized matrix? Are you then going to use the matrix to calculate differential abundance? In this tutorial, the authors (Susan Holmes and Joey McMurdie) refer to this tutorial for conducting differential abundance testing using the altered geometric mean formula, e.g.
QUESTION
I am running RNA Seq analysis on a dataset and I keep receiving this error when using DESeqDataSetFromMatrix. The df is counts data and the coldata is coldata.
...Error in DESeqDataSet(se, design = design, ignoreRank) : counts matrix should be numeric, currently it has mode: logical Here is the code being used:
ANSWER
Answered 2021-Sep-27 at 16:33I am not sure which version of R you use but a couple of things you can do is:
- to indicate the separator (
sep=","
) when uploading your data frame with counts - you can also convert a data frame to numeric matrix using
data.matrix()
- go through DESeq2 vignette thoroughly.
browseVignettes("DESeq2")
QUESTION
dds$Description <- select(dds, Description == "Mammary_Tumor", "Mammary_Normal")
ddstxnmam <- DESeq2:: DESeqDataSetFromMatrix(countData = dds,
colData = cd,
design = condition)
ddstxnmam <- DESeq2:: DESeq(ddstxnmam)
...ANSWER
Answered 2021-Sep-24 at 19:38select is for selecting columns, you are filtering here ( at least it looks like that since you did not provide any description and did not add a dataset).
QUESTION
I'm new to R and I'm trying to run R package EnhancedVolcano for generating a plot. My input csv file is a list of differentially expressed genes from DESeq2. The first column contains gene names that do not occur uniquely and so as to avoid duplicate rownames error
, I decided to make.unique by adding .1 etc to the column 1 names as below. However, I keep getting the error log2FoldChange is not numeric!
" for the below code
ANSWER
Answered 2021-Sep-02 at 10:29Here is a potential solution:
QUESTION
I am trying to run DESeq2 through rpy2 for the first time and am having some difficulties.
...ANSWER
Answered 2021-Aug-13 at 14:23If you open R and type:
QUESTION
I am using the magrittr
pipe %>%
to pipe an object into multiple arguments in the righthand side function, using curly braces to force :
ANSWER
Answered 2021-Aug-03 at 21:54We can use
QUESTION
I am trying to make a shiny dashboard. I have two datasets, and based upon the selection of the datasets figures will be generate in the tab panels. However, by default only the last dataset that has been loaded/read is selected and I cannot select the first dataset. Even though I have made it default selection.
Below is my code.
...ANSWER
Answered 2021-Aug-01 at 13:05Assuming you have access to both datasets, you plot them both and display the selection. Try this
QUESTION
I'm having issues trying to run a snakemake rule that invokes an R script. The relevant snakemake rule looks like this:
...ANSWER
Answered 2021-Jun-29 at 21:41The examples use script:
rather than shell:
So change to
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