seurat | scene simplification technology designed to process
kandi X-RAY | seurat Summary
kandi X-RAY | seurat Summary
The root node is a Capture object. Matrices are in row-major order.
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QUESTION
In the example below I get following error many times printed when switching back and forth between radio buttons iris and About-
...ANSWER
Answered 2021-Jun-02 at 13:20The error was coming from the esquisse
package unfortunately (https://github.com/dreamRs/esquisse/issues/164). It has been resolved now by the developer.
And second part of my question was answered by @bretauv. Thank you again!
QUESTION
My dataset is very strange. When I create the Seurat object and load the metadata for it, all of the values in the nCount_RNA are decimal values instead of integers. How should I interpret this? Is there an issue with the data itself or something I can do to work around this? I ask because later on in my analysis, the functions can't seem to find the nCount_RNA object, and I believe the decimal values are the reason why.
Here is the code I used to create this object:
...ANSWER
Answered 2021-Apr-14 at 18:05The file you read in, it is normalized somehow, and is definitely not the count data:
QUESTION
I have a Seurat object with defined clusters. I need to extract a list of all genes that are expressed by at least 10% of cells in my cluster. I need to repeat it for every cluster that I have, separately.
I know one code that could potentially extract genes expressed by at least 10% of cells from the whole Seurat:
...ANSWER
Answered 2021-Mar-27 at 00:50You could use lapply
to iterate over the factor levels of your clusters to subset and filter them individually and use setNames
to name the resulting list. Below is a reproducible example:
QUESTION
I am running R in OSX Mojave and am getting a following error when loading any packages with mgcv dependency;
...ANSWER
Answered 2021-Mar-24 at 13:01updating to the latest Brew version of r 4.0.4_2 and getting rid of /Library/Frameworks/R.framework cured it.
QUESTION
I have an object (Seurat object) an I need to get certain data out of it
...ANSWER
Answered 2021-Feb-23 at 17:02Solved it! I'm pretty disappointed by myself, because I didn't know this function existed:
QUESTION
I am trying to merge Seurat class objects that contain transcriptome count data (sparse matrix). I am relatively new to R, so any help/solutions is appreciated. I have added a screenshot of the data I'm working with.
...ANSWER
Answered 2021-Feb-06 at 23:16The machine used to process the data in the original question has a 64-bit Windows operating system running a 32-bit version of R. The result from memory.size()
shows that approximately 2.4Gb of RAM is available to the malloc()
function used by R. The 32-bit version of R on Windows can access a maximum of slightly less than 4Gb of RAM when running on 64-bit Windows, per the help for memory.size()
.
Memory Limits in R tells us that in 32-bit R on Windows it is usually not possible to allocate a single vector of 2Gb in size due to the fact that windows consumes some memory in the middle of the 2 Gb address space.
Once we load the data from the question, the zfbrainList
object consumes about 1.2Gb of RAM.
QUESTION
With this code I have this complexheatmap
...ANSWER
Answered 2021-Jan-10 at 21:30Heatmap(mat, border = T, show_column_names = F,
rect_gp = gpar(col = "white", lwd = 1),
column_split = response$response,
col = c("-2" = "blue", "0" = "grey", "1" = "red"),
heatmap_legend_param = list(at = c("-2", "0", "1"), labels = c("Del", "Netral", "Amp")),
show_column_dend = F,
show_row_dend = F,
left_annotation = left_annotation,
right_annotation = right_annotation,name = "CNV",
row_names_gp = gpar("fontface" = "italic")
)
QUESTION
{library(Seurat)
library(tidyverse)
library(purrr)}
dirNames <- unique(dirname(list.files("data/scRNA_CITE",
full.names = T,
recursive = T)))
######
#reading multiple directories and a resultant list
dat <- purrr::map(dirNames, Read10X)
names(dat) <- dirNames
#reading just one file
#M06 <- Read10X(data.dir = "data/m06/filtered_feature_bc_matrix/")
#renaming the rows of a list element (here named antibody capture) within one list works!
rownames(x = M06[["Antibody Capture"]]) <- gsub(pattern = "*_TotalSeqC", replacement = "",
x = rownames(x = M06[["Antibody Capture"]]))
#creating function for purrr
change_rname <- function(x){
rownames(x[["Antibody Capture"]]) <- sub(pattern = "*_TotalSeqC", replacement = "", x[["Antibody Capture"]])
}
# using the same function to rename multiple elements within multiple lists of a bigger list works temporarily BUT DOES not get saved within the bigger list
purrr::map(dat,
~change_rname(.x))
...ANSWER
Answered 2020-Dec-01 at 14:25Return the changed dataframe from the function.
QUESTION
ANSWER
Answered 2020-Oct-23 at 19:59We can use pivot_longer
QUESTION
I want to use OpenEXR in a Bazel project.
My WORKSPACE.bazel look like this:
...ANSWER
Answered 2020-Oct-04 at 19:17In the meantime, I was able to solve the problem. Base on the BUILD file file from seurat I took an up to date master version von OpenEXR and started to fix all issues. The final BUILD.bazel was tested successfully with Ubuntu 16.08 GCC, LLVM and Windows 10 VS2019.
I created my own bazel branch for the OpenEXR: https://github.com/Vertexwahn/openexr/tree/bazel
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