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library(devtools) | |
library(sleuth) | |
library(dplyr) | |
library("biomaRt") | |
#load annotation from ensembl | |
ensembl = useMart("ENSEMBL_MART_ENSEMBL",dataset="mmusculus_gene_ensembl", host="www.ensembl.org") | |
t2g <- biomaRt::getBM(attributes = c("ensembl_transcript_id", "ensembl_gene_id", "external_gene_name"), mart = ensembl) | |
t2g <- dplyr::rename(t2g, target_id = ensembl_transcript_id, ens_gene = ensembl_gene_id, ext_gene = external_gene_name) | |
#change this directory as your directory | |
base_dir = "/Volumes/Samsung_T1/RNASeq" | |
sample_id <- dir(file.path(base_dir,"results")) | |
kal_dirs <- sapply(sample_id, function(id) file.path(base_dir, "results", id)) | |
kal_dirs <- rev(kal_dirs) | |
s2c <- read.table(file.path(base_dir,"study_design.txt"), header = TRUE, stringsAsFactors=FALSE) | |
s2c <- dplyr::select(s2c, sample = run, condition) | |
s2c <- dplyr::mutate(s2c, path = kal_dirs) | |
so <- sleuth_prep(s2c, ~ condition, target_mapping = t2g) | |
so <- sleuth_fit(so) | |
so <- sleuth_wt(so, which_beta = 'conditionMII') | |
sleuth_live(so) |
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