View source: R/read_qpcr_data.R
read_lightcycler_1colour_raw | R Documentation |
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",
...
)
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 |
This function is a thin wrapper around readr::read_tsv.
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.
read_lightcycler_1colour_cq
read_lightcycler_1colour_raw(system.file("extdata/Edward_qPCR_Nrd1_calibration_2019-02-02.txt.gz",
package = "tidyqpcr"))
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