Nothing
## ----setup, include=FALSE-----------------------------------------------------
knitr::opts_chunk$set(echo = TRUE)
## ----eval=FALSE---------------------------------------------------------------
# if (!require("devtools")) {
# install.packages("devtools")
# }
# devtools::install_github("chencxxy28/InteRD")
## ----message=FALSE------------------------------------------------------------
#load
library(InteRD)
## ----message=FALSE------------------------------------------------------------
readRDSFromWeb <- function(ref) {
readRDS(gzcon(url(ref)))
}
seger <- readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/segerstolpe.rds")
baron <- readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/baron.rds")
xin<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/Xin_nonD.rds")
## ---- message=FALSE-----------------------------------------------------------
set.seed(1234567)
pseudo.seger<-generateBulk(seger[["sc.eset.qc"]], ct.varname = "cluster", sample = "sample", ct.sub = c("alpha","beta","delta","gamma"), nbulk = 40, low_s = 0.3, upp_s = 0.7)
truep<-pseudo.seger$true_p[complete.cases(pseudo.seger$true_p),]
## ---- message=FALSE,eval=FALSE------------------------------------------------
# set.seed(1234567)
# library(SCDC)
# ##ensemble of multiple reference sets
# #resuts based on SCDC
# pancreas.sc <- list(baron = baron$sc.eset.qc,
# xin = xin
# )
# SCDC_results<-SCDC_ENSEMBLE(bulk.eset = pseudo.seger$pseudo_eset, sc.eset.list = pancreas.sc, ct.varname = "cluster",
# sample = "sample", weight.basis =TRUE,truep = truep, ct.sub = c("alpha","beta","delta","gamma"), search.length = 0.02,grid.search=TRUE)
# comb<-SCDC_results$prop.only
# weight_matrix<-SCDC_results$w_table["mAD_Y",1:2]
# SCDC_ENSEMBLE_MAD<-SCDC:::wt_prop(weight_matrix,comb)
#
# # saveRDS(SCDC_ENSEMBLE_MAD,"/Users/chixiang.chen/Library/CloudStorage/OneDrive-UniversityofMarylandSchoolofMedicine/postdoc/postdoc/deconvolution/ref_based_rd/data_InteRD/SCDC_ENSEMBLE_MAD_seger.rds")
# # saveRDS(comb,"/Users/chixiang.chen/Library/CloudStorage/OneDrive-UniversityofMarylandSchoolofMedicine/postdoc/postdoc/deconvolution/ref_based_rd/data_InteRD/comb_seger.rds")
## ---- message=FALSE-----------------------------------------------------------
#results based on InteRD1
SCDC_ENSEMBLE_MAD<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/SCDC_ENSEMBLE_MAD_seger.rds")
comb<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/comb_seger.rds")
list_marker<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/list_markerbaron20.rds") #get markers selected from xin et al (2016)
lambda_option<-c(0,0.01,0.05,0.1,1,5,100)
cell_type_unique<-c("alpha","beta","delta","gamma")
InteRD1.output<-InteRD1(bulk.data =pseudo.seger$pseudo_eset,list_marker,cell_type_unique,comb_used=comb,lambda_option)
InteRD1<-InteRD.predict.prop(InteRD.output=InteRD1.output)
## ---- message=FALSE-----------------------------------------------------------
evaluate(SCDC_ENSEMBLE_MAD,pseudo.seger$true_p)$all.eva
evaluate(InteRD1,pseudo.seger$true_p)$all.eva
## ---- message=FALSE-----------------------------------------------------------
ave_est = pop.ct.prop.scRNA(scRNA=seger[["sc.eset.qc"]],cell_type_unique=cell_type_unique)$pop.ct.prop
ave_sd = pop.ct.prop.scRNA(scRNA=seger[["sc.eset.qc"]],cell_type_unique=cell_type_unique)$pop.ct.sd
lambda_option<-c(0,seq(from=1,to=20,length=4),seq(from=30,to=100,length=4),200,500,1000000^2)
InteRD2.output<-InteRD2(bulk.data=pseudo.seger$pseudo_eset,list_marker,cell_type_unique,comb_sampled=InteRD1,ave_est,ave_sd,lambda_option=lambda_option)
InteRD2<-InteRD.predict.prop(InteRD.output=InteRD2.output)
## ---- message=FALSE-----------------------------------------------------------
ref_free.output<-Ref_free(bulk.data=pseudo.seger$pseudo_eset,list_marker=list_marker,cell_type_unique=cell_type_unique)
reffree<-InteRD.predict.prop(InteRD.output=ref_free.output)
## ---- message=FALSE-----------------------------------------------------------
evaluate(SCDC_ENSEMBLE_MAD,pseudo.seger$true_p)$all.eva
evaluate(reffree,pseudo.seger$true_p)$all.eva
evaluate(InteRD1,pseudo.seger$true_p)$all.eva
evaluate(InteRD2,pseudo.seger$true_p)$all.eva
## ---- message=FALSE,eval=FALSE------------------------------------------------
# set.seed(1234567)
# pseudo.baron<-generateBulk(baron[["sc.eset.qc"]], ct.varname = "cluster", sample = "sample", ct.sub = c("alpha","beta","delta","gamma"), nbulk = 40, low_s = 0.3, upp_s = 0.7)
# truep<-pseudo.baron$true_p[complete.cases(pseudo.baron$true_p),]
## ---- message=FALSE,results='hide',eval=FALSE---------------------------------
# set.seed(1234567)
# ##ensemble of multiple reference sets
# #resuts based on SCDC
# pancreas.sc <- list(seger = seger$sc.eset.qc,
# xin = xin
# )
# SCDC_results<-SCDC_ENSEMBLE(bulk.eset = pseudo.baron$pseudo_eset, sc.eset.list = pancreas.sc, ct.varname = "cluster",
# sample = "sample", weight.basis =TRUE,truep = truep, ct.sub = c("alpha","beta","delta","gamma"), search.length = 0.02,grid.search=TRUE)
# comb<-SCDC_results$prop.only
# weight_matrix<-SCDC_results$w_table["mAD_Y",1:2]
# SCDC_ENSEMBLE_MAD<-SCDC:::wt_prop(weight_matrix,comb)
#
# # saveRDS(SCDC_ENSEMBLE_MAD,"/Users/chixiang.chen/Library/CloudStorage/OneDrive-UniversityofMarylandSchoolofMedicine/postdoc/postdoc/deconvolution/ref_based_rd/data_InteRD/SCDC_ENSEMBLE_MAD_baron.rds")
# # saveRDS(comb,"/Users/chixiang.chen/Library/CloudStorage/OneDrive-UniversityofMarylandSchoolofMedicine/postdoc/postdoc/deconvolution/ref_based_rd/data_InteRD/comb_baron.rds")
## ---- message=FALSE,eval=FALSE------------------------------------------------
# #results based on InteRD1
# SCDC_ENSEMBLE_MAD<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/SCDC_ENSEMBLE_MAD_baron.rds")
# comb<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/comb_baron.rds")
# list_marker<-readRDSFromWeb("https://github.com/chencxxy28/Data/raw/main/data_InteRD/list_markerbaron20.rds") #get markers selected from xin et al (2016)
# lambda_option<-c(0,0.01,0.05,0.1,1,5,100)
# cell_type_unique<-c("alpha","beta","delta","gamma")
# InteRD1.output<-InteRD1(bulk.data =pseudo.baron$pseudo_eset,list_marker,cell_type_unique,comb_used=comb,lambda_option)
# InteRD1<-InteRD.predict.prop(InteRD.output=InteRD1.output)
## ---- message=FALSE,eval=FALSE------------------------------------------------
# ave_est = pop.ct.prop.scRNA(scRNA=baron[["sc.eset.qc"]],cell_type_unique=cell_type_unique)$pop.ct.prop
# ave_sd = pop.ct.prop.scRNA(scRNA=baron[["sc.eset.qc"]],cell_type_unique=cell_type_unique)$pop.ct.sd
# lambda_option<-c(0,seq(from=1,to=20,length=4),seq(from=30,to=100,length=4),200,500,1000000^2)
# InteRD2.output<-InteRD2(bulk.data=pseudo.baron$pseudo_eset,list_marker,cell_type_unique,comb_sampled=InteRD1,ave_est,ave_sd,lambda_option=lambda_option)
# InteRD2<-InteRD.predict.prop(InteRD.output=InteRD2.output)
## ---- message=FALSE,eval=FALSE------------------------------------------------
# evaluate(SCDC_ENSEMBLE_MAD,pseudo.baron$true_p)$all.eva
# evaluate(InteRD1,pseudo.baron$true_p)$all.eva
# evaluate(InteRD2,pseudo.baron$true_p)$all.eva
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