arrow
返回

ICPD-A New Peak Detection Algorithm for LC/MS

delete2010-01-01
delete8
delete
OA
AI
J
Jianqiu Zhang *
W
William E. Haskins
DOI:10.1186/1471-2164-11-S3-S8delete
delete原文链接
delete分享
delete收藏
查看原文
摘要

摘要

En 中文
Background: The identification and quantification of proteins using label-free Liquid Chromatography/Mass Spectrometry (LC/MS) play crucial roles in biological and biomedical research. Increasing evidence has shown that biomarkers are often low abundance proteins. However, LC/MS systems are subject to considerable noise and sample variability, whose statistical characteristics are still elusive, making computational identification of low abundance proteins extremely challenging. As a result, the inability of identifying low abundance proteins in a proteomic study is the main bottleneck in protein biomarker discovery. Results: In this paper, we propose a new peak detection method called Information Combining Peak Detection (ICPD) for high resolution LC/MS. In LC/MS, peptides elute during a certain time period and as a result, peptide isotope patterns are registered in multiple MS scans. The key feature of the new algorithm is that the observed isotope patterns registered in multiple scans are combined together for estimating the likelihood of the peptide existence. An isotope pattern matching score based on the likelihood probability is provided and utilized for peak detection. Conclusions: The performance of the new algorithm is evaluated based on protein standards with 48 known proteins. The evaluation shows better peak detection accuracy for low abundance proteins than other LC/MS peak detection methods.
Keyword:
CHROMATOGRAPHY-MASS SPECTROMETRY
RESOLUTION LC-MS
PROTEOMICS
SOFTWARE
REDUCTION
SPECTRA
SUITE
AI总结

AI总结

对已上传原文的论文进行重点信息的提取,主要内容包括:简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。

期刊

BMC Genomics 封面图
BMC Genomics
IF:
3.7
论文数:
1.9W
被引数:
5.2W

机构

U
university of texas system
学者数:
18.5W
论文数: 15.6W
被引数: 210
引用论文

引用论文

暂无论文信息