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Find peaks in the chromatographic time domain of the profile matrix. For more details see do_findChromPeaks_matchedFilter().

Usage

# S4 method for class 'xcmsRaw'
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,
  scanrange = numeric()
)

Arguments

object

The xcmsRaw object on which peak detection should be performed.

fwhm

numeric(1) specifying the full width at half maximum of matched filtration gaussian model peak. Only used to calculate the actual sigma, see below.

sigma

numeric(1) specifying the standard deviation (width) of the matched filtration model peak.

max

numeric(1) representing the maximum number of peaks that are expected/will be identified per slice.

snthresh

numeric(1) defining the signal to noise cutoff to be used in the chromatographic peak detection step.

step

numeric(1) specifying the width of the bins/slices in m/z dimension.

steps

numeric(1) defining the number of bins to be merged before filtration (i.e. the number of neighboring bins that will be joined to the slice in which filtration and peak detection will be performed).

mzdiff

numeric(1) defining the minimum difference in m/z for peaks with overlapping retention times

index

logical(1) specifying whether indicies should be returned instead of values for m/z and retention times.

sleep

(DEPRECATED). The use of this parameter is highly discouraged, as it could cause problems in parallel processing mode.

scanrange

Numeric vector defining the range of scans to which the original object should be sub-setted before peak detection.

Value

A matrix, each row representing an intentified chromatographic peak.

References

Colin A. Smith, Elizabeth J. Want, Grace O'Maille, Ruben Abagyan and Gary Siuzdak. "XCMS: Processing Mass Spectrometry Data for Metabolite Profiling Using Nonlinear Peak Alignment, Matching, and Identification" Anal. Chem. 2006, 78:779-787. doi: 10.1021/ac051437y

Author

Colin A. Smith