#' Function to improve accuracy of DNA measurements for samples measured with both HS and BR dye
#'
#' @param hs_data data frame with HS dye data
#' @param br_data data frame with BR dye data
#'
#' @return data frame with more accurate DNA concentrations and microbial density measurements
#' @export
qubit_merger <- function(hs_data, br_data) {
hs_data_long <- hs_data %>% dplyr::mutate_(HS_fluorescence = "Fluorescence", HS_dna_concentration = "dna_concentration") %>% dplyr::select_("-Fluorescence", "-dna_concentration", "-microbial_density", "-total_dna", "-Experiment", "-ReaderWell") %>% dplyr::select( -dplyr::contains('vol'), -dplyr::contains('possible'))
br_data_long <- br_data %>% dplyr::mutate_(BR_fluorescence = "Fluorescence", BR_dna_concentration = "dna_concentration") %>% dplyr::select_("-Fluorescence", "-dna_concentration", "-microbial_density", "-total_dna", "-Experiment", "-ReaderWell") %>% dplyr::select( -dplyr::contains('vol'), -dplyr::contains('possible'))
combined_data <- dplyr::full_join(hs_data_long, br_data_long)
output_data <- combined_data %>% dplyr::mutate(
dna_concentration = ifelse(
test = (HS_dna_concentration < 75 & BR_dna_concentration < 50), yes = HS_dna_concentration, no = ifelse(
test = (BR_dna_concentration > 50 & HS_dna_concentration > 75), yes = BR_dna_concentration, no = (HS_dna_concentration + BR_dna_concentration)/2
)
),
dye_used = ifelse(
test = (HS_dna_concentration < 75 & BR_dna_concentration < 50), yes = "HS", no = ifelse(
test = (BR_dna_concentration > 50 & HS_dna_concentration > 75), yes = "BR", no = "Average"
)
),
total_dna = dna_concentration*scale_factor*0.1,
microbial_density = total_dna/SampleMass,
X16S_possible = (dna_concentration > 1.5 & dna_concentration > 0),
vol_needed_for_PCR = 400/dna_concentration,
water_volume_up_PCR = 200 - vol_needed_for_PCR,
metagenomics_possible = dna_concentration >= 20,
vol_needed_for_metagenomics = 600/dna_concentration,
water_volume_up_metagenomics = 30 - vol_needed_for_metagenomics
)
return(output_data)
}
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