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He creado la función sqlMultiSamples. También he adaptado la función sqlGenOVID para que sea usable para UM.

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Costa 2 years ago
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d863315655
1 changed files with 41 additions and 9 deletions
  1. +41
    -9
      sqlFunctions.R

+ 41
- 9
sqlFunctions.R

@ -47,23 +47,37 @@ sqlShowSamples<-function(conn=dta, nhcs=nhc.test, verb=F, dbtype){
} }
} }
sqlGenOVID<-function(conn=dta, nhcs=nhc.test, verb=T, sinc=F){
ovid<-sqlFetch(conn,"OVID")
sqlGenOVID<-function(conn=dta, nhcs=nhc.test, verb=T, sinc=F, dbtype){
if (dbtype == "OV"){
db<-c("dbcode"="OVID")
}
if (dbtype == "UM"){
db<-c("dbcode"="UMID")
}
dbid<-sqlFetch(conn,db["dbcode"])
new.nhc<-nhcs[!nhcs %in% ovid$NHC]
next.num<-gsub("OVID","",ovid$OVID) %>% as.numeric %>% max(na.rm=T)+1
new.nhc<-nhcs[!nhcs %in% dbid$NHC]
next.num<-gsub(db["dbcode"],"",dbid[,db["dbcode"]]) %>% as.numeric %>% max(na.rm=T)+1
last.num<-next.num+(length(new.nhc)-1) last.num<-next.num+(length(new.nhc)-1)
upd.ovid<-rbind(ovid,data.frame("NHC"=new.nhc, "OVID"=sprintf("OVID%04d",next.num:last.num)))
rownames(upd.ovid)<-as.character(1:nrow(upd.ovid))
upd.ovid<-filter(upd.ovid, NHC %in% new.nhc) %>% mutate(NHC=as.character(NHC))
newtab<-data.frame("NHC"=new.nhc, "ID"=sprintf("%s%04d",db["dbcode"],next.num:last.num)) %>% rename(!!db["dbcode"]:="ID")
if(dbtype=="OV"){
dbid<-rbind(dbid,newtab)
}
if(dbtype=="UM"){
dbid<-merge(dbid, newtab, all=T) %>% select(Id,NHC,UMID) %>% arrange(Id)
dbid$Id<-rownames(dbid)
}
rownames(dbid)<-as.character(1:nrow(dbid))
dbid<-filter(dbid, NHC %in% new.nhc) %>% mutate(NHC=as.character(NHC))
if (sinc){ if (sinc){
### !! Atención, esto cambia la base de datos: ### !! Atención, esto cambia la base de datos:
sqlSave(conn, upd.ovid, tablename="OVID", append = T)
sqlSave(conn, dbid, tablename=db["dbcode"], append = T)
print("La base ha sido actualizada.") print("La base ha sido actualizada.")
} }
if (verb){ if (verb){
return(upd.ovid)
return(dbid)
} }
} }
@ -149,3 +163,21 @@ sqlSincBD<-function(conn=dta, filetemp="QueryOV.xlsx", sinc.samples=F, sinc.clin
print("Tabla CLINICS sincronizada.") print("Tabla CLINICS sincronizada.")
} }
} }
sqlMultiSamples<-function(kbl=F, NHC=F){
query<-sqlQuery(dta, "SELECT M.UMID,U.NHC,M.FECHA_RECEPCION,M.CODIGO,C.CODIGO,R.CODIGO
FROM ((MUESTRAS M
LEFT OUTER JOIN CNAG C ON M.CODIGO=C.CODIGO)
LEFT OUTER JOIN RNADNA R ON M.CODIGO=R.CODIGO)
LEFT OUTER JOIN UMID U ON U.UMID=M.UMID") %>% rename("CNAG"="CODIGO.1","RNADNA"="CODIGO.2")
query<-query %>% mutate(
CNAG=case_when(!is.na(CNAG)~"X",TRUE~""),
RNADNA=case_when(!is.na(RNADNA)~"X",TRUE~"")
)
if (kbl==T){
query %>% kableExtra::kbl() %>% kableExtra::kable_styling(full_width = F, bootstrap_options = c("striped"))
}else{
return(query)
}
}

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