chipPCR: Toolkit of helper functions to pre-process amplification data

The chipPCR package is a toolkit of functions to preprocess amplification curve data. Amplification data can be obtained from conventional PCR reactions or isothermal amplification reactions. The package contains functions to normalize and baseline amplification curves, a routine to detect the start of an amplification reaction, several smoothers for amplification data, a function to distinguish positive and negative amplification reactions and a function to determine the amplification efficiency. The smoothers are based on LOWESS, moving average, cubic splines, Savitzky-Golay and others. In addition the first approximate approximate derivative maximum (FDM) and second approximate derivative maximum (SDM) can be calculated by a 5-point-stencil as quantification points from real-time amplification curves. chipPCR contains data sets of experimental nucleic acid amplification systems including the VideoScan HCU and a capillary convective PCR (ccPCR) system. The amplification data were generated by helicase dependent amplification (HDA) or polymerase chain reaction (PCR) under various temperature conditions. As detection system intercalating dyes (EvaGreen, SYBR Green) and hydrolysis probes (TaqMan) were used. The latest source code is available via:

Version: 0.0.7
Depends: R (≥ 3.0.0), methods
Imports: MASS, outliers, ptw, quantreg, Rfit, robustbase, shiny, signal
Suggests: MBmca (≥ 0.0.2)
Published: 2014-06-25
Author: Stefan Roediger, Michal Burdukiewicz
Maintainer: Stefan Roediger <stefan.roediger at>
License: GPL-3
NeedsCompilation: no
Materials: README ChangeLog
CRAN checks: chipPCR results


Reference manual: chipPCR.pdf
Package source: chipPCR_0.0.7.tar.gz
Windows binaries: r-devel:, r-release:, r-oldrel:
OS X Snow Leopard binaries: r-release: chipPCR_0.0.7.tgz, r-oldrel: chipPCR_0.0.7.tgz
OS X Mavericks binaries: r-release: chipPCR_0.0.7.tgz
Old sources: chipPCR archive

Reverse dependencies:

Reverse depends: MBmca
Reverse imports: dpcR