rutledge: qPCR data set by Rutledge et al. (2004)

In rutledge: Real-Time PCR Data Sets by Rutledge et al. (2004)

qPCR data set by Rutledge et al. (2004)

Description

Each data set comprises a six-point, ten-fold dilution series, repeated in five independent runs, for two different amplicons: K1/K2, 102 bp, and K3/K2, 218 bp. Fluorescence readings were exported after background subtraction via baseline averaging of the 5 cycles immediately preceding the cycles in which fluorescence was first detected. Please read the Materials and Methods section of Rutledge et al. (2004) for more details.

Format

A tibble with 10,800 rows and 10 variables:

plate

Plate identifier. Because one plate (run) was used per dilution series, plate values are simply numbered 1 thru 5.

well

Well identifier. Values are always NA (not available). This variable is kept nevertheless to be coherent with other data sets from other similar R data packages.

dye

The type of dye used. In this data set the values are always "SYBR", meaning SYBR Green I master mix (Roche).

target

Target identifier: the amplicon used, K1/K2 or K3/K2.

sample_type

Sample type (all curves are standards, i.e. "std").

replicate

Replicate identifier: 1 thru 4.

copies

Standard copy number.

dilution

Dilution factor. Higher number means greater dilution.

cycle

PCR cycle.

fluor

Raw fluorescence values.

Source

\Sexpr[results=rd]{tools:::Rd_expr_doi("10.1093/nar/gnh177")}

Examples

rutledge

rutledge documentation built on May 29, 2024, 7:35 a.m.