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Author SHA1 Message Date
marcelcosta 560540cf1a Commit in cytometry. 2023-10-10 12:35:43 +02:00
marcelcosta bd52e8c452 Corrección nombre de fecha de extracción. Solución de bug. 2023-02-02 16:54:09 +01:00
marcelcosta 43b807cc63 Corrección de la función de backup. 2022-07-04 11:09:20 +02:00
marcelcosta cb38ea347d Añadir notificación de sincronización y backup de nitrógeno. 2022-07-04 11:08:45 +02:00
marcelcosta 6671939939 Cambiar sistema de pedir contraseña. 2022-07-04 10:58:27 +02:00
marcelcosta a6f0c97d47 Añadir la opción de pasar la ruta de citometría en texto. 2022-04-20 15:34:54 +02:00
marcelcosta 56484a5903 Volver a meter unas línias borradas por error. 2022-04-20 12:13:27 +02:00
marcelcosta b5323436ec Boleanas en la app. 2022-04-20 09:49:37 +02:00
marcelcosta a57fb3aac8 Gates booleanas se hacen en R y no en Flowjo (que enlentece mucho el análisis). 2022-04-06 16:54:51 +02:00
marcelcosta dbb8e1ed0d Merge branch 'dev' 2022-04-06 12:42:53 +02:00
marcelcosta e6c2a32ddb Corregir exportar png IC 2022-04-06 12:42:31 +02:00
marcelcosta 51acdd0ece Merge branch 'dev' 2022-04-06 12:35:16 +02:00
marcelcosta dcbf4f8b9d Canvi en l'ordre de les dependències. 2022-04-06 12:32:41 +02:00
marcelcosta 001f64cc76 Merge branch 'dev' 2022-04-06 11:18:24 +02:00
marcelcosta e95caafe28 Cambio a pie chart para Visor IC. 2022-04-05 16:57:26 +02:00
marcelcosta f45ebfd106 Merge branch 'dev' 2022-04-05 10:09:30 +02:00
marcelcosta cb6c739d14 Para actualizar la tabla Poblaciones de citometría, permitir que falten poblaciones (de cara a agrupar diferentes paneles). 2022-04-05 10:08:26 +02:00
marcelcosta 20bf1d2c20 He añadido al visor de muestras el plot de IC. 2022-04-04 17:30:55 +02:00
marcelcosta a5581182c2 Añadir al visor de muestras el plot de poblaciones. 2022-04-04 17:15:12 +02:00
marcelcosta ab1684651e Completado procesado de datos de Checkpoint Inhibitors. 2022-04-04 17:14:42 +02:00
marcelcosta 67ba4921ca Añadir sección de citometría para tinciones de Poblaciones. 2022-04-04 15:40:54 +02:00
marcelcosta db6c07595c Cambiar etiquetas. 2022-04-04 11:37:56 +02:00
marcelcosta 35e4d31495 Iniciar sección citometría. Botón para el directorio. 2022-04-04 11:35:23 +02:00
marcelcosta 38aa06c4ee Añadir etiquetas para el código. 2022-04-04 11:34:43 +02:00
marcelcosta 38e902cef0 Merge branch 'dev' 2022-04-04 10:53:51 +02:00
marcelcosta 3492b7f7ef Corregir año en la fecha de tabla clinics 2022-04-01 12:26:42 +02:00
marcelcosta 44901be490 Corregir año en la fecha de tabla clinics 2022-04-01 12:26:04 +02:00
marcelcosta 3c8a69b21c Merge branch 'main' into dev 2022-04-01 12:21:02 +02:00
Costa 9b8f24ddd8 Corregir formato en las fechas de la plantilla CLINICS. 2022-03-31 14:18:46 +02:00
Costa ea45d8c845 merge with nitro 2022-03-31 13:40:47 +02:00
Costa 134133498b Corregir carga librerías para merge 2022-03-29 12:24:11 +02:00
Costa c9d09c44a2 Cambio de "Sincronizar" a "Actualizar" nitrógeno. 2022-03-28 14:52:42 +02:00
Costa b12ae3fd5f Introducción de un botón para actualizar nitrógeno. 2022-03-28 14:52:04 +02:00
Costa 2909f49eec Añadido plot para expresión de genes. 2022-03-28 12:49:29 +02:00
Costa b14fddf8fe Visor scRNAseq. 2022-03-22 16:29:04 +01:00
Costa 5bbd25c64d Empezar visor scRNAseq. 2022-03-22 14:26:33 +01:00
Costa 5ea3b493f4 Añadir la sincronización de tablas para CC. 2022-03-22 14:25:17 +01:00
+833 -12
View File
@@ -1,5 +1,15 @@
library(shiny) library(shiny)
library(rhandsontable) library(rhandsontable)
library(openCyto)
library(flowCore)
library(flowWorkspace)
library(CytoML)
library(ggcyto)
library(reshape2)
library(Matrix)
library(CitFuns)
library(BDCIT)
library(tidyverse)
print(getwd()) print(getwd())
source("../sqlFunctions.R", encoding = "UTF-8") source("../sqlFunctions.R", encoding = "UTF-8")
@@ -14,6 +24,8 @@ rna<-data.frame("UMID"="","UM"="")
sqlInitialize(ruta="../ruta_database.R") sqlInitialize(ruta="../ruta_database.R")
# UI ----
ui <- fluidPage( ui <- fluidPage(
# Application title # Application title
@@ -22,6 +34,8 @@ ui <- fluidPage(
#sidebarLayout( #sidebarLayout(
#Navbar #Navbar
navbarPage("BDAccess", navbarPage("BDAccess",
## Update ----
tabPanel("Update", tabPanel("Update",
sidebarPanel( sidebarPanel(
selectInput("dbtype", "", selected="UM", choices=c("UM", "OV","CC")), selectInput("dbtype", "", selected="UM", choices=c("UM", "OV","CC")),
@@ -47,26 +61,74 @@ ui <- fluidPage(
) )
) )
), ),
## Visor ----
tabPanel("Visor", tabPanel("Visor",
sidebarPanel( sidebarPanel(
radioButtons("nhc", label = h3("Código"), radioButtons("nhc", label = h3("Código"),
choices = list("NHC" = 1, "UMID/OVID" = 2, "UM/OV"=3), choices = list("NHC" = 1, "UMID/OVID" = 2, "UM/OV"=3),
selected = 2), selected = 2),
textInput("id", label = "ID", value = ""), textInput("id", label = "ID", value = ""),
actionButton("nitrosync", "Actualiza Nitrógeno")
), ),
mainPanel( mainPanel(
htmlOutput("report"), htmlOutput("report"),
h3("Nitrogen"), h3("Nitrogen"),
tableOutput("nitrogen") tableOutput("nitrogen"),
plotOutput("visorplot", height = "1000px")
) )
),
## Citometría ----
tabPanel("Citometría",
sidebarPanel(
selectInput("phenotype", "Tipo de análisis", selected="Pop", choices=c("Pop", "IC")),
),
mainPanel(
tabsetPanel(
tabPanel("Entrada",
actionButton("goButtonDir","Selecciona directorio fenotipo"),
textInput("cytopath", label="Directorio fenotipo", value=""),
textOutput("session"),
hr(),
actionButton("fcsconvert", "Convertir a fcs"),
hr(),
actionButton("pngexport", "Exportar informes"),
actionButton("popexport", "Actualizar BBDD")
),
tabPanel("Visor",
)
)
)
),
## scRNAseq ----
tabPanel("scRNAseq",
sidebarPanel(
textInput("sqlquery", label = "sqlquery", value = ""),
uiOutput("PATID"),
checkboxInput("sct_sel", "Mostrar filtrados"),
checkboxInput("cd45_chk", "Purificación CD45"),
textInput("genes", label="genes", value = "")
),
mainPanel(
tabsetPanel(
tabPanel("Table", tableOutput("sc_table")),
tabPanel("Plots",
plotOutput("sc_plot", height = "1000px"),
plotOutput("sc_expr"), height = "600px")
)
)
) )
) )
) )
# Define server logic required to draw a histogram # Define server logic required to draw a histogram
# Server ----
server <- function(input, output) { server <- function(input, output) {
## Update ## Update ----
values <- reactiveValues() values <- reactiveValues()
values[["DF"]]<-DF values[["DF"]]<-DF
@@ -82,24 +144,28 @@ server <- function(input, output) {
print(CCfile) print(CCfile)
if (input$dbtype == "UM"){ if (input$dbtype == "UM"){
dta<<-odbcConnectAccess2007(access.file = UMfile, dta<<-odbcConnectAccess2007(access.file = UMfile,
pwd = .rs.askForPassword("Enter password:")) pwd = getPass::getPass("Enter password:"))
} }
if (input$dbtype == "OV"){ if (input$dbtype == "OV"){
dta<<-odbcConnectAccess2007(access.file = OVfile, dta<<-odbcConnectAccess2007(access.file = OVfile,
pwd = .rs.askForPassword("Enter password:")) pwd = getPass::getPass("Enter password:"))
} }
if (input$dbtype == "CC"){ if (input$dbtype == "CC"){
dta<<-odbcConnectAccess2007(access.file = CCfile, dta<<-odbcConnectAccess2007(access.file = CCfile,
pwd = .rs.askForPassword("Enter password:")) pwd = getPass::getPass("Enter password:"))
} }
print(dta) print(dta)
if (input$backup == T){ if (input$backup == T){
if (! input$dbtype %in% c("UM","OV")){ if (! input$dbtype %in% c("UM","OV")){
sqlBackUp(bu.dir="CC_BU") sqlBackUp(dbfile = CCfile, bu.dir="CC_BU")
}else{
sqlBackUp()
} }
if (input$dbtype == "UM"){
sqlBackUp(dbfile = UMfile)
}
if (input$dbtype == "OV"){
sqlBackUp(dbfile = OVfile)
}
print("Back up realizado.")
} }
}) })
@@ -181,7 +247,9 @@ server <- function(input, output) {
output$CLINICS <- renderRHandsontable({ output$CLINICS <- renderRHandsontable({
if (!is.null(CLINICS)){ if (!is.null(CLINICS)){
rhandsontable(values[["CLINICS"]], stretchH = "all", readOnly = F, useTypes = T) rhandsontable(values[["CLINICS"]], stretchH = "all", readOnly = F, useTypes = T) %>%
hot_col(values[["CLINICS"]] %>% select(lubridate::is.Date) %>% colnames,
dateFormat = "DD/MM/YYYY", type = "date")
} }
}) })
@@ -316,7 +384,7 @@ server <- function(input, output) {
new.samp.df<-data.frame("NHC"=values[["DF"]]$NHC, "samples"=new.samp) %>% merge(sqlFetch(dta,"OVID"), all.x=T) %>% arrange(samples) new.samp.df<-data.frame("NHC"=values[["DF"]]$NHC, "samples"=new.samp) %>% merge(sqlFetch(dta,"OVID"), all.x=T) %>% arrange(samples)
samples.exp<-merge(samples %>% slice(0), new.samp.df %>% select(-NHC), all=T) %>% select(colnames(samples)) %>% arrange(samples) samples.exp<-merge(samples %>% slice(0), new.samp.df %>% select(-NHC), all=T) %>% select(colnames(samples)) %>% arrange(samples)
if (today==TRUE){ if (today==TRUE){
samples.exp$IQ_date<-format(Sys.Date(), "%d/%m/%y") samples.exp$Date_extraction<-format(Sys.Date(), "%d/%m/%y")
} }
nhc.table<-values[["DF"]] nhc.table<-values[["DF"]]
@@ -520,9 +588,81 @@ server <- function(input, output) {
sqlSave(dta, clinics.new, tablename="CLINICS", append = T, varTypes = varTypes, rownames = F) sqlSave(dta, clinics.new, tablename="CLINICS", append = T, varTypes = varTypes, rownames = F)
print("Tabla CLINICS sincronizada.") print("Tabla CLINICS sincronizada.")
} }
if (input$dbtype %in% c("CC")){
## Nuevas entradas en MUESTRAS
nsamples<-values[["samples"]] %>% nrow
upd.samples<-values[["samples"]]
if (nrow(upd.samples) > 0){rownames(upd.samples)<-(nsamples+1):(nsamples+nrow(upd.samples)) %>% as.character}
if (nrow(upd.samples) > 0){
upd.samples$FECHA_RECEPCION<-lubridate::parse_date_time(upd.samples$FECHA_RECEPCION, c("d/m/Y","d/m/y")) %>% as.Date()
upd.samples$TIPO<-as.character(upd.samples$TIPO)
upd.samples$OBS<-as.character(upd.samples$OBS)
### !! Atención, esto cambia la base de datos:
sqlSave(dta, upd.samples, tablename="MUESTRAS", append = T, varTypes = c("FECHA_RECEPCION"="Date"), rownames = F)
print("Tabla MUESTRAS sincronizada.")
}
## Entradas modificadas en CLINICOS
upd.clinics<-values[["CLINICS"]]
PATID.mod<-upd.clinics$PATID[upd.clinics$PATID %in% (sqlFetch(dta, "CLINICOS") %>% pull(PATID))]
rnames<-sqlFetch(dta, "CLINICOS") %>% filter(PATID %in% PATID.mod) %>% rownames
clinics.mod<-upd.clinics %>% filter(PATID %in% PATID.mod) %>% select(-NHC)
rownames(clinics.mod)<-rnames
### !! Atención, esto cambia la base de datos:
fechas<-colnames(clinics.mod)[grepl("date|MET_DX|DoB", colnames(clinics.mod), ignore.case = T)]
for (i in fechas){
clinics.mod[,i]<-lubridate::parse_date_time(clinics.mod[,i], c("d/m/Y","d/m/y")) %>% as.Date()
}
sqlUpdate(dta, clinics.mod,"CLINICOS", index="PATID")
print("Tabla CLINICOS modificada.")
## Nuevas entradas en CLINICOS
nsamples.clin<-sqlFetch(dta, "CLINICOS") %>% nrow
PATID.new<-upd.clinics$PATID[!upd.clinics$PATID %in% (sqlFetch(dta, "CLINICOS") %>% pull(PATID))]
clinics.new<-upd.clinics %>% filter(PATID %in% PATID.new) %>% select(-NHC)
if (length(PATID.new) > 0){rownames(clinics.new)<-(nsamples.clin+1):(nsamples.clin+nrow(clinics.new)) %>% as.character}
### !! Atención, esto cambia la base de datos:
fechas<-colnames(clinics.new)[grepl("date|MET_DX|DoB", colnames(clinics.new), ignore.case = T)]
varTypes<-rep("Date",length(fechas))
names(varTypes)<-fechas
for (i in fechas){
clinics.new[,i]<-lubridate::parse_date_time(clinics.new[,i], c("d/m/Y","d/m/y","Y-m-d")) %>% as.Date()
}
sqlSave(dta, clinics.new, tablename="CLINICOS", append = T, varTypes = varTypes, rownames = F)
print("Tabla CLINICOS sincronizada.")
## Nuevas entradas en CNAG
if (nrow(values[["cnag"]]) > 0){
cnag.sync<-values[["cnag"]]
fechas<-colnames(cnag.sync)[sqlFetch(dta, "CNAG") %>% sapply(lubridate::is.POSIXct)]
varTypes<-rep("Date",length(fechas))
names(varTypes)<-fechas
print(fechas)
for (i in fechas){
cnag.sync[,i]<-lubridate::parse_date_time(cnag.sync[,i], c("d/m/Y","d/m/y","Y-m-d")) %>% as.Date()
}
sqlSave(dta, cnag.sync, tablename="CNAG", append = T, varTypes = varTypes, rownames = F)
}
## Nuevas entradas en RNADNA
if (nrow(values[["rna"]]) > 0){
rna.sync<-values[["rna"]]
fechas<-colnames(rna.sync)[sqlFetch(dta, "RNADNA") %>% sapply(lubridate::is.POSIXct)]
varTypes<-rep("Date",length(fechas))
names(varTypes)<-fechas
for (i in fechas){
rna.sync[,i]<-lubridate::parse_date_time(rna.sync[,i], c("d/m/Y","d/m/y","Y-m-d")) %>% as.Date()
}
sqlSave(dta, rna.sync, tablename="RNADNA", append = T, varTypes = varTypes, rownames = F)
}
}
}) })
## Visor
## Visor ----
output$report<-renderUI({ output$report<-renderUI({
samples<-sqlFetch(dta, "samples") samples<-sqlFetch(dta, "samples")
@@ -604,6 +744,687 @@ server <- function(input, output) {
nitro nitro
}) })
observeEvent(input$nitrosync, {
if (input$dbtype == "UM"){
## Copia de backup
if (!dir.exists(NitroRoute)){
dir.create(NitroRoute)
print(paste0("Back Up directory ", NitroRoute, " created"))
}
write.xlsx(
sqlFetch(dta, "NITROGEN"),
file=paste0(NitroRoute, format(Sys.time(), format="%Y%m%d"),"-","UM-Nitrogen.xlsx")
)
print("Backup Creado.")
table<-read.xlsx(paste0(gsub("/BU_NITRO/", "", NitroRoute),"/Nitrogen_ICO.xlsx"))
table.um<-table %>% filter( grepl("UM|MU", Nombre) | grepl("Met|Prim|hep|Enn",Nombre, ignore.case = T) |
Nombre == "TILs f. 21/09/20" | Nombre == "TILS DISG f. 03/07/20")
table.um<-add_column(table.um,.before=1, "CODIGO"=str_extract(table.um$Nombre, "UM[0-9]{4}"))
table.samp<-sqlQuery(dta, "SELECT U.NHC,M.* FROM MUESTRAS M INNER JOIN UMID U ON M.UMID=U.UMID")
table.samp$FECHA_RECEPCION<-table.samp$FECHA_RECEPCION+24*60*60
table.um<-add_column(table.um, .after=1,
"FECHA"=str_extract(table.um$Nombre, "[0-9]{2}[\\./][0-9]{2}[\\./][0-9]{2}") %>% gsub("\\.","/",.))
table.um$FECHA<-as.POSIXct(table.um$FECHA, format="%d/%m/%y")
table.um<-merge(table.um, table.samp %>% select(CODIGO,FECHA_RECEPCION), by.x="FECHA", by.y="FECHA_RECEPCION", all.x=T)
table.um<-table.um %>% mutate(CODIGO=case_when(is.na(CODIGO.x)~CODIGO.y, TRUE~CODIGO.x), .before=1) %>% select(-CODIGO.x,-CODIGO.y)
table.um[table.um$Nombre == "MU Met f. 10/02/20","CODIGO"]<-"UM0009"
table.um[table.um$Nombre == "TILs Diss Met","CODIGO"]<-"UM0020"
table.um[table.um$Nombre == "UM Met","CODIGO"]<-"UM0020"
table.um[table.um$Nombre == "UM MET NHC 11489341","CODIGO"]<-"UM0044"
table.um[table.um$Nombre == "UM Primary 20278822","CODIGO"]<-"UM0029"
table.um[table.um$Nombre == "Hip Nod Hep NHC11489341","CODIGO"]<-"UM0044"
## Actualización
sqlDrop(dta, "NITROGEN")
sqlSave(dta, table.um %>% select(-FECHA) %>% filter(!is.na(CODIGO)), tablename="NITROGEN", rownames=F)
print("Tabla Actualizada.")
}
if (input$dbtype == "OV"){
## Copia de backup
if (!dir.exists(NitroRoute)){
dir.create(NitroRoute)
print(paste0("Back Up directory ", NitroRoute, " created"))
}
write.xlsx(
sqlFetch(dta, "NITROGEN"),
file=paste0(NitroRoute, format(Sys.time(), format="%Y%m%d"),"-","OV-Nitrogen.xlsx")
)
print("Backup Creado.")
## Lectura del excel
table<-read.xlsx(paste0(gsub("/BU_NITRO/", "", NitroRoute),"/Nitrogen_ICO.xlsx"))
table.ov<-table %>% filter(grepl("OV",Nombre))
table.ov<-filter(table.ov, !grepl("OVA",Nombre))
table.ov<-add_column(table.ov,.before=1, "CODIGO"=str_extract(table.ov$Nombre, "OV[0-9]{4}"))
table.ov[table.ov$Nombre == "Ascitis OV","CODIGO"]<-"OV2105"
table.ov<-table.ov %>% add_column(SampType=NA, .after=1)
table.ov[grepl("TIL",table.ov$Nombre, ignore.case = T),"SampType"]<-"TILs"
table.ov[grepl("frag",table.ov$Nombre, ignore.case = T)|grepl("frag",table.ov$Observaciones, ignore.case = T),"SampType"]<-"FRAG"
table.ov[grepl("slide",table.ov$Nombre, ignore.case = T)|grepl("slide",table.ov$Observaciones, ignore.case = T),"SampType"]<-"SLIDE"
table.ov[(is.na(table.ov$SampType) | !(table.ov$SampType == "TILs")) &
(grepl("disg|diss",table.ov$Nombre, ignore.case = T)|
grepl("disg|diss",table.ov$Observaciones, ignore.case = T)),"SampType"]<-"DISG"
table.ov[table.ov$Nombre == "Ascitis OV", "SampType"]<-"ASC"
table.ov[20:25,"SampType"]<-"DISG"
table.ov[63:68,"SampType"]<-"DISG"
## Actualización
sqlDrop(dta, "NITROGEN")
sqlSave(dta, table.ov, tablename="NITROGEN", rownames=F)
print("Tabla Actualizada.")
}
})
output$visorplot<-renderPlot({
if (input$nhc == 3){
data<-sqlFetch(dta, "IC") %>% filter(samples == input$id)
data1<-data %>% gather(phen, value, -samples, -Population)
data1$phen<-gsub("p","+",data1$phen)
data1$phen<-gsub("n","-",data1$phen)
data1$phen<-gsub("_"," ",data1$phen)
data1$phen<-gsub("n","-",data1$phen, fixed = T)
data1$phen<-gsub("p","+",data1$phen, fixed = T)
data1$phen<-gsub("_"," ",data1$phen)
data1[data1$value < 0.5, "phen"]<-"Other"
data1$phen<-gsub("[A-Z]*-*[0-9T]- *", "", data1$phen)
data1$phen<-gsub("+ $", "", data1$phen)
data1$phen[data1$phen == ""]<-"All Negative"
# data1<-data1 %>% filter(value > 0.5)
data1["phen1"]<-"PD1"
data1[!grepl("PD1+", data1$phen),"phen1"]<-NA
data1["phen2"]<-"TIM3"
data1[!grepl("TIM3+", data1$phen),"phen2"]<-NA
data1["phen3"]<-"CTLA4"
data1[!grepl("CTLA4+", data1$phen),"phen3"]<-NA
data1["phen4"]<-"TIGIT"
data1[!grepl("TIGIT+", data1$phen),"phen4"]<-NA
data1["phen5"]<-"LAG3"
data1[!grepl("LAG3+", data1$phen),"phen5"]<-NA
data1<-data1 %>% arrange(desc(value))
data2<-data1 %>% filter(!phen %in% c("All Negative","Other"))
data1<-rbind(data2, data1 %>% filter(phen %in% c("All Negative","Other")) %>% arrange(desc(phen)))
data_cd8<-data1 %>% filter(Population == "CD8")
data_cd4<-data1 %>% filter(Population == "CD4")
data_cd8$ymax<-cumsum(data_cd8$value)
data_cd8$ymin<-c(0, head(data_cd8$ymax, n=-1))
data_cd4$ymax<-cumsum(data_cd4$value)
data_cd4$ymin<-c(0, head(data_cd4$ymax, n=-1))
data1<-rbind(data_cd8, data_cd4)
color<-c(c("CTLA4+ LAG3+ PD1+ TIGIT+ TIM3+"="black","All Negative"="grey90","Other"="grey50", "PD1+"="#C07AFF", "CTLA4+"="#3EB3DE","TIM3+"="#5EF551","LAG3+"="#DEBB3E","TIGIT+"="#FA7055"),
c("CTLA4+ PD1+"="#6666FF","PD1+ TIM3+"="#849CA8", "LAG3+ PD1+"="#C47F9F","PD1+ TIGIT+"="#D259AA", "CTLA4+ TIM3+"="#4ED498", "CTLA4+ LAG3+"="#8EB78E", "CTLA4+ TIGIT+"="#9C929A", "LAG3+ TIM3+"="#9ED848", "TIGIT+ TIM3+"="#ACB353", "LAG3+ TIGIT+"="#EC964A"),
c("CTLA4+ PD1+ TIGIT+"="#B86B6A","CTLA4+ PD1+ TIGIT+ TIM3+"="#B81515","LAG3+ PD1+ TIGIT+"="#007D8A", "PD1+ TIGIT+ TIM3+"="#D64545", "LAG3+ PD1+ TIGIT+ TIM3+"="#0f5860", "LAG3+ TIGIT+ TIM3+"="#50cad3"))
basic.color<-color[c("PD1+","TIGIT+","TIM3+","CTLA4+","LAG3+")]
names(basic.color)<-c("PD1","TIGIT","TIM3","CTLA4","LAG3")
# Make the plot
g1<-ggplot(data1)+
facet_wrap(.~Population)+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=4.5, xmin=0), fill=color[data1$phen])+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=5.4, xmin=5, fill=factor(phen1, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=5.9, xmin=5.5, fill=factor(phen4, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=6.4, xmin=6, fill=factor(phen2, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=6.9, xmin=6.5, fill=factor(phen3, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=7.4, xmin=7, fill=factor(phen5, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
scale_fill_manual(values = basic.color, na.value="#FFFFFF00", drop=F, limits=c("PD1","TIGIT","TIM3","CTLA4","LAG3"), name="IC")+
coord_polar(theta="y") + # Try to remove that to understand how the chart is built initially
xlim(c(0, 8)) +# Try to remove that to see how to make a pie chart
theme_classic()+
theme(strip.background = element_blank(),
strip.text = element_text(size=12, face="bold"),
axis.line = element_blank(),
axis.ticks = element_blank(),
plot.margin = margin(-200,0,0,0),
axis.text = element_blank())
# df.color<-data.frame("phen"=names(color), "color"=color)
# df.color<-rbind(
# df.color %>% filter(!phen %in% c("All Negative","Other")) %>% arrange(phen),
# df.color %>% filter(phen %in% c("All Negative","Other")) %>% arrange(desc(phen))
# )
#
# g2<-ggplot(df.color, aes(phen, 1))+
# geom_tile(fill=df.color$color)+
# scale_x_discrete(limits=df.color$phen)+
# ggtitle("Phenotype Combination")+
# theme(axis.text.x = element_text(angle=90, hjust=1, vjust=0.5),
# axis.text.y = element_blank(),
# axis.ticks = element_blank(),
# axis.title = element_blank(),
# panel.background = element_blank())+
# coord_equal()
# g_IC<-ggpubr::ggarrange(g1,g2,ncol=1)
g_IC<-g1
pops<-sqlFetch(dta, "POPULATIONS")
g_pop<-pops %>%
dplyr::filter(sample == input$id) %>%
gather(pop,value,-sample, -code, -fc_time) %>%
# mutate(pop=factor(pop, levels=c("CD45pos_Alive","T_cells","CD8","CD4","DN","NK", "B_cells",
# "CD45neg_LDneg","EpCAMneg_HLAIneg","EpCAMneg_HLAIpos","EpCAMpos_HLAIpos"))) %>%
# mutate(pop=factor(pop, levels=c("CD45pos_Alive","T_cells","CD8","CD4","DN","NK", "B_cells",
# "CD45neg_LDneg","EpCAMneg_HLAIneg","EpCAMneg_HLAIpos","EpCAMpos_HLAIpos"))) %>%
mutate(value=as.numeric(gsub(",",".",value))) %>%
ggplot(aes(pop, value))+
geom_bar(stat="identity", color="black", fill="grey70")+
labs(title = input$id, y="% parent", x="")+
theme_bw()+
theme(axis.text.x = element_text(angle=90, hjust=1, vjust=0.5))
# tl<-sqlFetch(dta, "IC") %>% filter(samples == input$id)
#
# mtl<-melt(tl, variable.name = "Receptors")
# mtl$Receptors<-as.character(mtl$Receptors) #Para poder depurar bien el texto, lo pasamos a tipo character
# mtl$Receptors<-gsub("n","-",mtl$Receptors, fixed = T)
# mtl$Receptors<-gsub("p","+",mtl$Receptors, fixed = T)
# mtl$Receptors<-gsub("_"," ",mtl$Receptors)
# mtl[mtl$value < 1, "Receptors"]<-"Other"
# mtl$Receptors<-gsub("[A-Z]*-*[0-9T]- *", "", mtl$Receptors)
# mtl$Receptors<-gsub("+ $", "", mtl$Receptors)
# mtl$Receptors[mtl$Receptors == ""]<-"All Negative"
#
# mtl$Receptors<-factor(mtl$Receptors)
# mtl$Population<-factor(mtl$Population, levels = c("CD8", "CD4"))
#
# # colorCount<-length(unique(mtl$Receptors))
# # getPalette = colorRampPalette(RColorBrewer::brewer.pal(12, "Set3"))
#
# color<-c(c("CTLA4+ LAG3+ PD1+ TIGIT+ TIM3+"="black","All Negative"="white","Other"="grey50", "PD1+"="#C07AFF", "CTLA4+"="#3EB3DE","TIM3+"="#5EF551","LAG3+"="#DEBB3E","TIGIT+"="#FA7055"),
# c("CTLA4+ PD1+"="#6666FF","PD1+ TIM3+"="#849CA8", "LAG3+ PD1+"="#C47F9F","PD1+ TIGIT+"="#D259AA", "CTLA4+ TIM3+"="#4ED498", "CTLA4+ LAG3+"="#8EB78E", "CTLA4+ TIGIT+"="#9C929A", "LAG3+ TIM3+"="#9ED848", "TIGIT+ TIM3+"="#ACB353", "LAG3+ TIGIT+"="#EC964A"),
# c("CTLA4+ PD1+ TIGIT+"="#B86B6A","CTLA4+ PD1+ TIGIT+ TIM3+"="#B81515","LAG3+ PD1+ TIGIT+"="#007D8A", "PD1+ TIGIT+ TIM3+"="#D64545", "LAG3+ PD1+ TIGIT+ TIM3+"="#0f5860", "LAG3+ TIGIT+ TIM3+"="#50cad3"))
#
# g_IC<-ggplot(mtl, aes(samples, value, fill=Receptors))+
# geom_bar(stat="summary", fun="sum",color="black")+
# labs(x="Patient", y="% CD8+", fill="")+
# facet_grid(.~Population)+
# scale_fill_manual(values = color[levels(mtl$Receptors)[levels(mtl$Receptors) %in% unique(mtl$Receptors)]])+
# theme_bw()+
# theme(axis.text.x=element_text(angle=45, hjust=1))
ggpubr::ggarrange(g_pop, g_IC, heights = c(0.4, 0.6), ncol = 1)
}
})
## Citometría ----
observe({
if(input$goButtonDir > 0){
if (input$cytopath == ""){
cito_dir<<-choose.dir() %>% gsub("\\","/",. ,fixed=T) %>% paste0("/")
}else{
cito_dir<<-input$cytopath %>% gsub("\\","/",. ,fixed=T) %>% gsub("/$", "", .) %>% paste0("/")
}
output$session <- renderText(
cito_dir
)
}
})
observeEvent(input$fcsconvert,{
route<-cito_dir
files<-list.files(route, ".LMD")
for (lmd in files){
fcs<-read.FCS(paste0(route,lmd), dataset = 2)
# fcs@parameters$desc<-c("FS-A","SS-A", paste("FL",1:10,"-A", sep = ""), "TIME")
# fcs@parameters$desc<-c("FS-H","FS-A","FS-W","SS-H","SS-A","TIME", paste("FL",1:10,"-A", sep = ""))
keyword(fcs)['$FIL']<-paste0(gsub(".LMD","",lmd), ".fcs")
write.FCS(fcs, paste0(route, gsub(".LMD","",lmd), ".fcs"))
}
})
observeEvent(input$pngexport,{
if (input$phenotype == "Pop"){
route<-cito_dir
ws<-open_flowjo_xml(paste0(route,"Populations.wsp"))
gs<-flowjo_to_gatingset(ws, name="All Samples")
sampleNames(gs)<-sapply(sampleNames(gs), function(x) strsplit(x, "Pop ")[[1]][2]) %>%
gsub("[[:space:]][0-9]*.fcs_.[0-9]*","", . , perl = T)
for (samp in sampleNames(gs)){
print(samp)
p<-autoplot(gs[[samp]], bins=64)
ggsave(paste0(route, samp,".pop.png"),p,width = 10, height = 10)
}
}
if (input$phenotype == "IC"){
route<-stringi::stri_enc_tonative(cito_dir)
ws<-open_flowjo_xml(paste0(route,"IC.wsp"))
gs<-flowjo_to_gatingset(ws, name="All Samples")
sampleNames(gs)<-sapply(sampleNames(gs), function(x) strsplit(x, "ICs ")[[1]][2]) %>%
gsub("[[:space:]][0-9]*.fcs_.[0-9]*","", . , perl = T)
bool.comb<-apply(
expand.grid(c("","!"), c("","!"),c("","!"), c("","!"), c("","!")),
1,
function(x) paste0(x[1],"CTLA4 & ",x[2],"LAG3 & ",x[3],"PD1 & ",x[4], "TIGIT & ",x[5], "TIM3")
)
bool.name<-apply(
expand.grid(c("+","-"), c("+","-"),c("+","-"), c("+","-"), c("+","-")),
1,
function(x) paste0("CTLA4",x[1]," LAG3",x[2]," PD1",x[3]," TIGIT",x[4]," TIM3",x[5])
)
print("Booleanos CD8")
for (i in 1:length(bool.comb)){
call<-substitute(booleanFilter(v), list(v=as.symbol(bool.comb[i])))
boolgate<-eval(call)
gs_pop_add(gs, boolgate, parent="CD8", name = bool.name[i])
}
print("Booleanos CD4")
for (i in 1:length(bool.comb)){
call<-substitute(booleanFilter(v), list(v=as.symbol(bool.comb[i])))
boolgate<-eval(call)
gs_pop_add(gs, boolgate, parent="CD4", name = bool.name[i])
}
recompute(gs)
names<-sampleNames(gs) %>% gsub("ab|Ab|AB|iso|Iso|ISO| ","",.) %>% unique()
nodes<-gs_get_pop_paths(gs)
# nodes<-gsub("â\u0081»", "-", nodes)
# nodes<-gsub("â\u0081º", "+", nodes)
nodes<-nodes[grepl("CTLA4", nodes)]
nodes<-nodes[!grepl("CD4$|CD8$|CTLA4$|TIM3$|PD1$|LAG3$|TIGIT$", nodes)]
pop<-gs_pop_get_stats(gs, nodes=nodes,type="percent") %>% as.data.frame %>% mutate(percent=percent*100)
pop$percent<-round(pop$percent, digits=2)
# pop$pop<-gsub("â\u0081»", "n", pop$pop)
# pop$pop<-gsub("â\u0081º", "p", pop$pop)
pop$pop<-gsub("-", "n", pop$pop, fixed=T)
pop$pop<-gsub("+", "p", pop$pop, fixed=T)
pop$pop<-gsub(" ", "_", pop$pop)
pop["Type"]<-"ab"
pop[grepl("iso|ISO|Iso",pop$sample),"Type"]<-"iso"
pop$sample<-gsub("iso|ISO|Iso|ab|AB|Ab| ","",pop$sample)
pop_sp<-pop %>% spread(Type, percent)
pop_sp["Net"]<-pop_sp$ab
pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"Net"]<-pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"ab"]-pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"iso"]
pop_sp$Net[pop_sp$Net < 0]<-0
pop_sp["Population"]<-str_extract(pop_sp$pop, "/CD[4,8]{1}/") %>% gsub("/","",.)
pop_sp$pop<-sapply(strsplit(pop_sp$pop, "/"), tail, 1)
pop_sp<-pop_sp %>% select(-ab,-iso) %>% spread(pop,Net)
pop_sp$CTLA4n_LAG3n_PD1n_TIGITn_TIM3n<- pop_sp %>% select(-CTLA4n_LAG3n_PD1n_TIGITn_TIM3n) %>% group_by(sample,Population) %>%
gather(pop, value, -sample,-Population) %>% summarise(n=100-sum(value)) %>% pull(n)
if (input$dbtype == "OV"){
pop_sp <- rename(pop_sp, "samples"="sample")
}
if (input$dbtype %in% c("UM", "CC")){
pop_sp <- rename(pop_sp, "CODIGO"="sample")
}
pop_sql<-sqlFetch(dta, "IC") %>% slice(0)
pop_sp<-pop_sp %>% merge(pop_sql, all=T) %>% select(colnames(pop_sql))
for (id in names){
print(id)
iso<-sampleNames(gs)[grepl(id, sampleNames(gs)) & grepl("iso|Iso|ISO",sampleNames(gs))]
ab<-sampleNames(gs)[grepl(id, sampleNames(gs)) & grepl("ab|Ab|AB",sampleNames(gs))]
if (input$dbtype == "OV"){
data<-pop_sp %>% filter(samples == id)
data1<-data %>% gather(phen, value, -samples, -Population)
}
if (input$dbtype %in% c("UM", "CC")){
data<-pop_sp %>% filter(CODIGO == id)
data1<-data %>% gather(phen, value, -CODIGO, -Population)
}
data1$phen<-gsub("p","+",data1$phen)
data1$phen<-gsub("n","-",data1$phen)
data1$phen<-gsub("_"," ",data1$phen)
data1$phen<-gsub("n","-",data1$phen, fixed = T)
data1$phen<-gsub("p","+",data1$phen, fixed = T)
data1$phen<-gsub("_"," ",data1$phen)
data1[data1$value < 0.5, "phen"]<-"Other"
data1$phen<-gsub("[A-Z]*-*[0-9T]- *", "", data1$phen)
data1$phen<-gsub("+ $", "", data1$phen)
data1$phen[data1$phen == ""]<-"All Negative"
# data1<-data1 %>% filter(value > 0.5)
data1["phen1"]<-"PD1"
data1[!grepl("PD1+", data1$phen),"phen1"]<-NA
data1["phen2"]<-"TIM3"
data1[!grepl("TIM3+", data1$phen),"phen2"]<-NA
data1["phen3"]<-"CTLA4"
data1[!grepl("CTLA4+", data1$phen),"phen3"]<-NA
data1["phen4"]<-"TIGIT"
data1[!grepl("TIGIT+", data1$phen),"phen4"]<-NA
data1["phen5"]<-"LAG3"
data1[!grepl("LAG3+", data1$phen),"phen5"]<-NA
data1<-data1 %>% arrange(desc(value))
data2<-data1 %>% filter(!phen %in% c("All Negative","Other"))
data1<-rbind(data2, data1 %>% filter(phen %in% c("All Negative","Other")) %>% arrange(desc(phen)))
data_cd8<-data1 %>% filter(Population == "CD8")
data_cd4<-data1 %>% filter(Population == "CD4")
data_cd8$ymax<-cumsum(data_cd8$value)
data_cd8$ymin<-c(0, head(data_cd8$ymax, n=-1))
data_cd4$ymax<-cumsum(data_cd4$value)
data_cd4$ymin<-c(0, head(data_cd4$ymax, n=-1))
data1<-rbind(data_cd8, data_cd4)
color<-c(c("CTLA4+ LAG3+ PD1+ TIGIT+ TIM3+"="black","All Negative"="grey90","Other"="grey50", "PD1+"="#C07AFF", "CTLA4+"="#3EB3DE","TIM3+"="#5EF551","LAG3+"="#DEBB3E","TIGIT+"="#FA7055"),
c("CTLA4+ PD1+"="#6666FF","PD1+ TIM3+"="#849CA8", "LAG3+ PD1+"="#C47F9F","PD1+ TIGIT+"="#D259AA", "CTLA4+ TIM3+"="#4ED498", "CTLA4+ LAG3+"="#8EB78E", "CTLA4+ TIGIT+"="#9C929A", "LAG3+ TIM3+"="#9ED848", "TIGIT+ TIM3+"="#ACB353", "LAG3+ TIGIT+"="#EC964A"),
c("CTLA4+ PD1+ TIGIT+"="#B86B6A","CTLA4+ PD1+ TIGIT+ TIM3+"="#B81515","LAG3+ PD1+ TIGIT+"="#007D8A", "PD1+ TIGIT+ TIM3+"="#D64545", "LAG3+ PD1+ TIGIT+ TIM3+"="#0f5860", "LAG3+ TIGIT+ TIM3+"="#50cad3"))
basic.color<-color[c("PD1+","TIGIT+","TIM3+","CTLA4+","LAG3+")]
names(basic.color)<-c("PD1","TIGIT","TIM3","CTLA4","LAG3")
# Make the plot
g_coex<-ggplot(data1)+
facet_grid(factor(Population, levels=c("CD8","CD4"))~.)+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=4.5, xmin=0), fill=color[data1$phen])+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=5.4, xmin=5, fill=factor(phen1, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=5.9, xmin=5.5, fill=factor(phen4, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=6.4, xmin=6, fill=factor(phen2, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=6.9, xmin=6.5, fill=factor(phen3, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
geom_rect(aes(ymax=ymax, ymin=ymin, xmax=7.4, xmin=7, fill=factor(phen5, levels=c("PD1","TIGIT","TIM3","CTLA4","LAG3"))))+
scale_fill_manual(values = basic.color, na.value="#FFFFFF00", drop=F, limits=c("PD1","TIGIT","TIM3","CTLA4","LAG3"), name="IC")+
coord_polar(theta="y") + # Try to remove that to understand how the chart is built initially
xlim(c(0, 8)) +# Try to remove that to see how to make a pie chart
theme_classic()+
theme(strip.background = element_blank(),
strip.text = element_text(size=12, face="bold"),
axis.line = element_blank(),
axis.ticks = element_blank(),
# plot.margin = margin(-200,0,0,0),
axis.text = element_blank())
nodes<-gs_get_pop_paths(gs)
nodes_parent<-nodes[!grepl("CTLA4|LAG3|PD1|TIGIT|TIM3|root$", nodes)]
nodes_cd4<-nodes[grepl("CTLA4$|LAG3$|PD1$|TIGIT$|TIM3$", nodes) & grepl("/CD4/",nodes)]
nodes_cd8<-nodes[grepl("CTLA4$|LAG3$|PD1$|TIGIT$|TIM3$", nodes) & grepl("/CD8/",nodes)]
# g1<-ggcyto_arrange(autoplot(gs[[ab]], nodes_parent, bins=128), nrow=1)
# g2<-ggcyto_arrange(autoplot(gs[[iso]], nodes_cd8, bins=64), nrow=1)
# g3<-ggcyto_arrange(autoplot(gs[[ab]], nodes_cd8, bins=64), nrow=1)
# g4<-ggcyto_arrange(autoplot(gs[[iso]], nodes_cd4, bins=64), nrow=1)
# g5<-ggcyto_arrange(autoplot(gs[[ab]], nodes_cd4, bins=64), nrow=1)
g1<-ggcyto_arrange(autoplot(gs[[ab]], nodes_parent), nrow=1)
g2<-ggcyto_arrange(autoplot(gs[[iso]], nodes_cd8), nrow=1)
g3<-ggcyto_arrange(autoplot(gs[[ab]], nodes_cd8), nrow=1)
g4<-ggcyto_arrange(autoplot(gs[[iso]], nodes_cd4), nrow=1)
g5<-ggcyto_arrange(autoplot(gs[[ab]], nodes_cd4), nrow=1)
g_dots<-gridExtra::gtable_rbind(g1,g2,g3,g4,g5)
g_all<-ggpubr::ggarrange(g_dots, g_coex, nrow=1, widths=c(0.65,0.35))
ggsave(paste0(route,id,".IC.png"), g_all, width = 14, height = 10)
}
}
})
observeEvent(input$popexport,{
if (input$phenotype == "Pop"){
route<-cito_dir
ws<-open_flowjo_xml(paste0(route,"Populations.wsp"))
gs<-flowjo_to_gatingset(ws, name="All Samples")
sampleNames(gs)<-sapply(sampleNames(gs), function(x) strsplit(x, "Pop ")[[1]][2]) %>%
gsub("[[:space:]][0-9]*.fcs_.[0-9]*","", . , perl = T)
nodes<-sapply(strsplit(gs_get_pop_paths(gs), "/"), tail, 1)
nodes<-nodes[grepl("_",nodes)]
pop<-gs_pop_get_stats(gs, nodes=nodes,type="percent") %>% as.data.frame %>% mutate(percent=percent*100)
pop[,"pop"]<-gsub("_","",pop$pop)
pop$pop<-gsub(" ","_",pop$pop)
pop$pop<-gsub("+","pos",pop$pop, fixed=T)
pop$pop<-gsub("-","neg",pop$pop, fixed=T)
pop<-rename(pop, "samples"="sample")
pop$percent<-round(pop$percent, digits=2)
pop_sp<-pop %>% spread(pop, percent)
pop_sql<-sqlFetch(dta, "POPULATIONS") %>% slice(0)
pop_sp<-pop_sp %>% merge(pop_sql, all=T) %>% select(colnames(pop_sql))
vartypes<-rep("Number", pop_sp %>% select(-samples) %>% colnames %>% length)
names(vartypes)<-pop_sp %>% select(-samples) %>% colnames
sqlSave(dta, pop_sp, tablename="POPULATIONS", append = T, varTypes = vartypes, rownames = F)
print("Tabla POPULATIONS sincronizada.")
}
if (input$phenotype == "IC"){
route<-cito_dir
ws<-open_flowjo_xml(paste0(route,"IC.wsp"))
gs<-flowjo_to_gatingset(ws, name="All Samples")
sampleNames(gs)<-sapply(sampleNames(gs), function(x) strsplit(x, "ICs ")[[1]][2]) %>%
gsub("[[:space:]][0-9]*.fcs_.[0-9]*","", . , perl = T)
bool.comb<-apply(
expand.grid(c("","!"), c("","!"),c("","!"), c("","!"), c("","!")),
1,
function(x) paste0(x[1],"CTLA4 & ",x[2],"LAG3 & ",x[3],"PD1 & ",x[4], "TIGIT & ",x[5], "TIM3")
)
bool.name<-apply(
expand.grid(c("+","-"), c("+","-"),c("+","-"), c("+","-"), c("+","-")),
1,
function(x) paste0("CTLA4",x[1]," LAG3",x[2]," PD1",x[3]," TIGIT",x[4]," TIM3",x[5])
)
for (i in 1:length(bool.comb)){
print("Booleanos CD8")
call<-substitute(booleanFilter(v), list(v=as.symbol(bool.comb[i])))
boolgate<-eval(call)
gs_pop_add(gs, boolgate, parent="CD8", name = bool.name[i])
}
for (i in 1:length(bool.comb)){
print("Booleanos CD4")
call<-substitute(booleanFilter(v), list(v=as.symbol(bool.comb[i])))
boolgate<-eval(call)
gs_pop_add(gs, boolgate, parent="CD4", name = bool.name[i])
}
recompute(gs)
nodes<-gs_get_pop_paths(gs)
# nodes<-gsub("â\u0081»", "-", nodes)
# nodes<-gsub("â\u0081º", "+", nodes)
nodes<-nodes[grepl("CTLA4", nodes)]
nodes<-nodes[!grepl("CD4$|CD8$|CTLA4$|TIM3$|PD1$|LAG3$|TIGIT$", nodes)]
pop<-gs_pop_get_stats(gs, nodes=nodes,type="percent") %>% as.data.frame %>% mutate(percent=percent*100)
pop$percent<-round(pop$percent, digits=2)
# pop$pop<-gsub("â\u0081»", "n", pop$pop)
# pop$pop<-gsub("â\u0081º", "p", pop$pop)
pop$pop<-gsub("-", "n", pop$pop, fixed=T)
pop$pop<-gsub("+", "p", pop$pop, fixed=T)
pop$pop<-gsub(" ", "_", pop$pop)
pop["Type"]<-"ab"
pop[grepl("iso|ISO|Iso",pop$sample),"Type"]<-"iso"
pop$sample<-gsub("iso|ISO|Iso|ab|AB|Ab| ","",pop$sample)
pop_sp<-pop %>% spread(Type, percent)
pop_sp["Net"]<-pop_sp$ab
pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"Net"]<-pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"ab"]-pop_sp[!grepl("CTLA4n_LAG3n_PD1n_TIGITn_TIM3n",pop_sp$pop),"iso"]
pop_sp$Net[pop_sp$Net < 0]<-0
pop_sp["Population"]<-str_extract(pop_sp$pop, "/CD[4,8]{1}/") %>% gsub("/","",.)
pop_sp$pop<-sapply(strsplit(pop_sp$pop, "/"), tail, 1)
pop_sp<-pop_sp %>% select(-ab,-iso) %>% spread(pop,Net)
pop_sp$CTLA4n_LAG3n_PD1n_TIGITn_TIM3n<- pop_sp %>% select(-CTLA4n_LAG3n_PD1n_TIGITn_TIM3n) %>% group_by(sample,Population) %>%
gather(pop, value, -sample,-Population) %>% summarise(n=100-sum(value)) %>% pull(n)
if (input$dbtype == "OV"){
pop_sp <- rename(pop_sp, "samples"="sample")
}
if (input$dbtype %in% c("UM", "CC")){
pop_sp <- rename(pop_sp, "CODIGO"="sample")
}
pop_sql<-sqlFetch(dta, "IC") %>% slice(0)
pop_sp<-pop_sp %>% merge(pop_sql, all=T) %>% select(colnames(pop_sql))
if (input$dbtype == "OV"){
vartypes<-rep("Number", pop_sp %>% select(-samples, -Population) %>% colnames %>% length)
names(vartypes)<-pop_sp %>% select(-samples, -Population) %>% colnames
}
if (input$dbtype %in% c("UM", "CC")){
vartypes<-rep("Number", pop_sp %>% select(-CODIGO, -Population) %>% colnames %>% length)
names(vartypes)<-pop_sp %>% select(-CODIGO, -Population) %>% colnames
}
sqlSave(dta, pop_sp, tablename="IC", append = T, varTypes = vartypes, rownames = F)
print("Tabla IC sincronizada.")
}
})
## scRNAseq ----
output$PATID = renderUI({
observeEvent(input$goButton, {})
sc_cod<-sqlFetch(dta, "CNAG") %>% pull(CODIGO)
selectizeInput("sc_cod", "CÓDIGO", sc_cod, multiple = T)
})
output$sc_table<-renderTable({
if (input$sct_sel){
if (input$sqlquery != ""){
print(input$sqlquery)
sqlQuery(dta, input$sqlquery)
}else{
if (!is.null(input$sc_cod)){
sqlFetch(dta, "CNAG") %>% filter(CODIGO %in% input$sc_cod)
}else{
sqlFetch(dta, "CNAG")
}
}
}else{
sqlFetch(dta, "CNAG")
}
})
output$sc_plot <-renderPlot({
meta<<-readRDS(paste0(scRNAseqRoute,"metadata_full_object.rds"))
if (input$sqlquery != ""){
sc_codigos<-sqlQuery(dta, input$sqlquery) %>% pull(CNAG_NAME)
}else{
if (!is.null(input$sc_cod)){
sc_codigos<-sqlFetch(dta, "CNAG") %>% filter(CODIGO %in% input$sc_cod) %>% pull(CNAG_NAME)
}else{
sc_codigos<-sqlFetch(dta, "CNAG") %>% pull(CNAG_NAME)
}
}
sc_codigos<-gsub(" _","_", sc_codigos )
sc_codigos<-gsub("_ ","_", sc_codigos )
sc_codigos<-gsub(" ","_", sc_codigos )
meta<-meta %>% mutate(sample2=gsub("_CD45", "", sample)) %>% filter(sample2 %in% sc_codigos)
if (isFALSE(input$cd45_chk)){ meta<-meta %>% filter(!grepl("_CD45", sample))}
g1<-ggplot(meta, aes(coord_x, coord_y, color=predicted.id))+
geom_point(size=0.2)+
guides(colour = guide_legend(override.aes = list(size=2)))+
theme_bw()+
theme(aspect.ratio = 1)
meta_perc<-meta %>% group_by(sample, predicted.id) %>% summarise(N=n()) %>% mutate(N=perc(N)) %>%
spread(predicted.id, N) %>% gather("predicted.id","N",-sample) %>% mutate(N=case_when(is.na(N)~0,TRUE~N))
g2<-ggheatmap(meta_perc, "sample","predicted.id", "N", color = "grey50")
ggpubr::ggarrange(g1,g2, ncol=1, heights = c(0.3, 0.7))
})
output$sc_expr <-renderPlot({
if (input$genes != ""){
expr<-readRDS(paste0(scRNAseqRoute,"expression_full_object.rds"))
genes<-strsplit(input$genes, ",")[[1]]
if (length(genes) > 1){
df.expr<-as.data.frame(as.matrix(expr[genes,]))
df.expr["Gene"]<-rownames(df.expr)
mdf.expr<-melt(df.expr)
}else{
df.expr<-as.data.frame(t(as.matrix(expr[genes[1],])))
df.expr["Gene"]<-genes[1]
mdf.expr<-melt(df.expr)
}
alldata<-merge(meta, mdf.expr, by.x="barcode", by.y = "variable")
}
# order <- clustsort(alldata %>% spread(Gene, value) %>% select(predicted.id, all_of(genes)) %>%
# group_by(predicted.id) %>% summarise(across(all_of(genes), mean)) %>% as.data.frame)
#
# g1<-ggplot(alldata, aes(predicted.id, value, fill=predicted.id))+
# geom_violin(scale = "width")+
# geom_jitter(width=0.2, size=0.1, alpha=0.3)+
# scale_x_discrete(limits=order$x)+
# guides(fill=F)+
# facet_wrap(.~Gene)+
# theme_bw()+
# theme(axis.text.x = element_text(angle=90, hjust=1, vjust = 0.5))
g2<-ggheatmap(alldata, x="predicted.id",y="Gene",value="value", color="grey")+coord_equal()
# ggpubr::ggarrange(g1,g2, ncol=1)
g2
})
} }
# Run the application # Run the application