Processing MALDI mass spectra to improve mass spectral direct tissue analysis

被引:154
作者
Norris, Jeremy L.
Cornett, Dale S.
Mobley, James A.
Andersson, Malin
Seeley, Erin H.
Chaurand, Pierre
Caprioli, Richard M.
机构
[1] Vanderbilt Univ, Mass Spectrometry Res Ctr, Sch Med, Nashville, TN 37232 USA
[2] Prot Discovery Inc, Knoxville, TN 37902 USA
[3] Univ Alabama, Dept Surg, Div Urol, Birmingham, AL 35294 USA
关键词
profiling; imaging; mass spectrometry; MALDI; pre-processing;
D O I
10.1016/j.ijms.2006.10.005
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Profiling and imaging biological specimens using MALDI mass spectrometry has significant potential to contribute to our understanding and diagnosis of disease. The technique is efficient and high-throughput providing a wealth of data about the biological state of the sample from a very simple and direct experiment. However, in order for these techniques to be put to use for clinical purposes, the approaches used to process and analyze the data must improve. This study examines some of the existing tools to baseline subtract, normalize, align, and remove spectral noise for MALDI data, comparing the advantages of each. A preferred workflow is presented that can be easily implemented for data in ASCII format. The advantages of using such an approach are discussed for both molecular profiling and imaging mass spectrometry. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:212 / 221
页数:10
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