This is the data from "export in text format" from the LightCycler software. The other data format, .ixo, can be converted to .txt format by the LightCycler software.

read_lightcycler_1colour_raw(
  filename,
  skip = 2,
  col_names = c("well", "sample_info", "program_no", "segment_no", "cycle", "time",
    "temperature", "fluor_raw"),
  col_types = "ccffinnn",
  ...
)

Arguments

filename

file name

skip

number of lines to skip, defaults to 2

col_names

names to give to columns

col_types

data types of columns

...

other arguments to pass to read_tsv, if needed

Value

tibble containing raw data, with default column names:

well: the well of the plate, e.g. A1

sample_info: this is the "Sample" field entered in LightCycler software, defaults to "Sample X"

program_no: the number of the cycler program, for 2-step PCR defaults to 1 = melt, 2 = amplify, 3 = melt.

segment_no: the number of the segment of the cycler program, e.g. hold/raise/lower temperature

cycle: the cycle number, for programs with repeated cycles (i.e. amplification)

time: the time of fluorescence reading acquisition (in what units???)

temperature: the temperature of the block at fluorescence acquisition

fluor_raw: the raw fluorescence reading in "arbitrary units". For SYBR safe, this would be 483nm excitation, 533nm emission.

Details

This function is a thin wrapper around readr::read_tsv.

See also

read_lightcycler_1colour_cq