Randolph T W, Yasui Y
Department of Biostatistics, University of Washington, Seattle, Washington 98195, USA.
Biometrics. 2006 Jun;62(2):589-97. doi: 10.1111/j.1541-0420.2005.00504.x.
This work addresses the problem of extracting signal content from protein mass spectrometry data. A multiscale decomposition of these spectra is used to focus on local scale-based structure by defining scale-specific features. Quantification of features is accompanied by an efficient method for calculating the location of features which avoids estimation of signal-to-noise ratios or bandwidths. Scale-based histograms serve as spectral-density-like functions indicating the regions of high density of features in the data. These regions provide bins within which features are quantified and compared across samples. As a preliminary step, the locations of prominent features within coarse-scale bins may be used for a crude registration of spectra. The multiscale decomposition, the scale-based feature definition, the calculation of feature locations, and subsequent quantification of features are carried out by way of a translation-invariant wavelet analysis.
这项工作解决了从蛋白质质谱数据中提取信号内容的问题。通过定义特定尺度的特征,对这些光谱进行多尺度分解,以关注基于局部尺度的结构。特征量化伴随着一种计算特征位置的有效方法,该方法避免了信噪比或带宽的估计。基于尺度的直方图用作类似光谱密度的函数,指示数据中特征高密度的区域。这些区域提供了用于量化特征并在样本间进行比较的区间。作为初步步骤,粗尺度区间内突出特征的位置可用于光谱的粗略配准。多尺度分解、基于尺度的特征定义、特征位置的计算以及随后的特征量化均通过平移不变小波分析来进行。