\name{findPeaks.matchedFilter-methods} \docType{methods} \alias{findPeaks.matchedFilter} \alias{findPeaks.matchedFilter,xcmsRaw-method} \title{Feature detection in the chromatographic time domain} \description{ Find peaks in extracted the chromatographic time domain of the profile matrix. } \section{Methods}{ \describe{ \item{object = "xcmsRaw"}{ \code{ findPeaks.matchedFilter(object, fwhm = 30, sigma = fwhm/2.3548, max = 5, snthresh = 10, step = 0.1, steps = 2, mzdiff = 0.8 - step*steps, index = FALSE, sleep = 0) } } }} \arguments{ \item{object}{\code{xcmsRaw} object} \item{fwhm}{ full width at half maximum of matched filtration gaussian model peak. Only used to calculate the actual sigma, see below. } \item{sigma}{ standard deviation (width) of matched filtration model peak } \item{max}{ maximum number of peaks per extracted ion chromatogram } \item{snthresh}{signal to noise ratio cutoff} \item{step}{step size to use for profile generation} \item{steps}{number of steps to merge prior to filtration} \item{mzdiff}{ minimum difference in m/z for peaks with overlapping retention times } \item{index}{ return indicies instead of values for m/z and retention times } \item{sleep}{ number of seconds to pause between plotting peak finding cycles } } \value{ A matrix with columns: \item{mz}{ weighted (by intensity) mean of peak m/z across scans } \item{mzmin}{ m/z of minimum step } \item{mzmax}{ m/z of maximum step } \item{rt}{ retention time of peak midpoint } \item{rtmin}{ leading edge of peak retention time } \item{rtmax}{ trailing edge of peak retention time } \item{into}{ integrated area of original (raw) peak } \item{intf}{ integrated area of filtered peak } \item{maxo}{ maximum intensity of original (raw) peak } \item{maxf}{ maximum intensity of filtered peak } \item{i}{ rank of peak identified in merged EIC (<= \code{max}) } \item{sn}{ signal to noise ratio of the peak } } \author{Colin A. Smith, \email{csmith@scripps.edu}} \seealso{ \code{\link{findPeaks-methods}} \code{\link{xcmsRaw-class}} } \keyword{methods}