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82 changes: 39 additions & 43 deletions modules/nf-core/ctree/templates/main_script.R
Original file line number Diff line number Diff line change
Expand Up @@ -61,52 +61,48 @@ add_dummy_driver = function(input_table, variant_colname, is_driver_colname) {
return(input_table)
}

initialize_ctree_obj_pyclone = function(ctree_input) {
driver_cluster = unique(ctree_input[which(ctree_input["is.driver"]==TRUE),c("cluster")])
# the CCF table must report CCF values for each cluster and sample
# cluster | nMuts | is.driver | is.clonal | sample1 | sample2 | ...
CCF_table = ctree_input %>%
dplyr::select(sample_id, cluster, nMuts, is.driver, is.clonal, CCF) %>%
dplyr::mutate(is.driver=ifelse(is.driver=="", FALSE, TRUE)) %>%
dplyr::filter(cluster!="Tail") %>%
dplyr::group_by(cluster) %>%
dplyr::mutate(is.driver=any(is.driver)) %>%
dplyr::filter(any(CCF>0)) %>%
dplyr::ungroup() %>%
unique() %>%
tidyr::pivot_wider(names_from="sample_id", values_from="CCF", values_fill=0)

# the driver table must contain patient and variant IDs and report clonality and driver status
# patientID | variantID | is.driver | is.clonal | cluster | sample1 | sample2 | ...
drivers_table = ctree_input %>%
dplyr::filter(cluster %in% CCF_table[["cluster"]]) %>%
dplyr::mutate(is.driver=as.logical(is.driver)) %>%
dplyr::select(patientID, sample_id, variantID, cluster, is.driver, is.clonal, CCF) %>%
dplyr::filter(is.driver==TRUE) %>%
dplyr::mutate(variantID=replace(variantID, is.na(variantID), "")) %>%
tidyr::pivot_wider(names_from="sample_id", values_from="CCF", values_fill=0) %>%
dplyr::mutate(cluster=as.character(cluster))

samples = unique(ctree_input[["sample_id"]]) # if multisample, this is a list
patient = unique(ctree_input[["patientID"]])

CCF_table = add_dummy_driver(CCF_table, variant_colname="variantID", is_driver_colname="is.driver") %>%
dplyr::mutate(cluster=as.character(cluster))

if (nrow(drivers_table)==0) {
drivers_table = CCF_table %>%
dplyr::filter(is.driver) %>%
dplyr::select(-nMuts) %>%
dplyr::mutate(patientID=patient)
}

ctree_init = list("CCF_table"=CCF_table,
"drivers_table"=drivers_table,
"samples"=samples,
"patient"=patient)
return(ctree_init)
initialize_ctree_obj_pyclone = function(ctree_input) {
ctree_input = add_dummy_driver(ctree_input, variant_colname="variantID", is_driver_colname="is.driver")


# the CCF table must report CCF values for each cluster and sample
# cluster | nMuts | is.driver | is.clonal | sample1 | sample2 | ...
CCF_table = ctree_input %>%
dplyr::select(sample_id, cluster, nMuts, is.driver, is.clonal, CCF) %>%
dplyr::mutate(is.driver=replace(is.driver, is.driver=="", "FALSE")) %>%
dplyr::mutate(is.driver=as.logical(is.driver)) %>%
dplyr::filter(cluster!="Tail") %>%
dplyr::mutate(cluster=as.character(cluster)) %>%
dplyr::group_by(cluster) %>%
dplyr::mutate(is.driver=any(is.driver)) %>%
dplyr::filter(any(CCF>0)) %>%
dplyr::ungroup() %>% unique() %>%
tidyr::pivot_wider(names_from="sample_id", values_from="CCF", values_fill=0)

# the driver table must contain patient and variant IDs and report clonality and driver status
# patientID | variantID | is.driver | is.clonal | cluster | sample1 | sample2 | ...
drivers_table = ctree_input %>%
dplyr::filter(cluster %in% CCF_table[["cluster"]]) %>%
dplyr::mutate(is.driver=as.logical(is.driver)) %>%
dplyr::mutate(cluster=as.character(cluster)) %>%
dplyr::select(patientID, sample_id, variantID, cluster, is.driver, is.clonal, CCF) %>%
dplyr::filter(is.driver==TRUE) %>%
dplyr::mutate(variantID=replace(variantID, is.na(variantID), "")) %>%
tidyr::pivot_wider(names_from="sample_id", values_from="CCF", values_fill=0)

samples = unique(ctree_input[["sample_id"]]) # if multisample, this is a list
patient = unique(ctree_input[["patientID"]])


ctree_init = list("CCF_table"=CCF_table,
"drivers_table"=drivers_table,
"samples"=samples,
"patient"=patient)
return(ctree_init)
}


if ( grepl(".rds\$", tolower("$ctree_input")) ) {
best_fit = readRDS("$ctree_input")
do_fit = TRUE
Expand Down
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