View source: R/measure_dna_concentration.R
measure_dna_concentration | R Documentation |
Measure DNA concentration for using qubit to quantify DNA
measure_dna_concentration(plate_reader_file, standards_plate_reader_file = plate_reader_file, standard_wells, dye_used, qubit_volume = 2, elution_volume = 100, plate_size = 96, plate_name = "DNA_Plate", print_standard_curve = FALSE, omit_standards = NULL)
plate_reader_file |
relative location to relevant plate reader file (accepts excel files) |
standards_plate_reader_file |
relative location to the plate reader file containing the standards (if it is the same as the plate you want to quantify, it is not necessary to explicitly specify |
standard_wells |
a vector containing the wells that contain the standards in increasing concentration (e.g. c("A01", "A02", "A03", "A04", "A05", "A06", "A07", "A08")) - needs to be sequential. If you need to exclude any standards, use omit_standards |
dye_used |
"BR" or "HS" to specify quantification with HS or BR dye |
qubit_volume |
volume of sample used for quantification (default = 2) |
elution_volume |
volume of your sample (used to compute total DNA in sample, default = 100) |
plate_size |
size of plate (default = 96, alternative is 384 - not tested yet) |
plate_name |
name to give plate (helps when using multiple plates) |
print_standard_curve |
TRUE or FALSE to indicate whether or not to save a .pdf image containing the standard curve |
omit_standards |
pass along a well location to exclude from standard analysis (helpful for when one fails) |
table with DNA concentrations for each sample, given the input parameters
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