Publications:Improved protein identification in mammalian cells using a new automatic peak detection algorithm

From ISLAB/CAISR
Revision as of 22:22, 14 February 2020 by Slawek (talk | contribs) (Created page with "<div style='display: none'> == Do not edit this section == </div> {{PublicationSetupTemplate|Author=Thorsteinn Rögnvaldsson, Jari Häkkinen, Jim Samuelsson, Claes Lindberg, G...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigationJump to search

Do not edit this section

Property "Publisher" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user. Property "Author" has a restricted application area and cannot be used as annotation property by a user.

Keep all hand-made modifications below

Title Improved protein identification in mammalian cells using a new automatic peak detection algorithm
Author
Year 2002
PublicationType Conference Paper
Journal
HostPublication Proceedings - 50th ASMS Conference on Mass Spectrometry and Allied Topics : June 2 - 6, 2002, Orlando, Florida
Conference 50th ASMS Conference on Mass Spectrometry and Allied Topics, Orlando, Florida, United States, June 2-6, 2002
DOI
Diva url http://hh.diva-portal.org/smash/record.jsf?searchId=1&pid=diva2:1393211
Abstract

A comparison of two automatic peak detection algorithms is presented. One algorithm comes with the Voyager 5 Data ExplorerTM program, the other is a new algorithm called Pepex® (short for PEptide Peak Extractor) from BioBridge Computing. The peak sets selected with both tools have been compared, against each other and against manual peak selections, on a large set of mass spectra obtained after tryptic in gel digestion of 2D-gel samples from human fetal fibroblasts. It is shown how much variation there is in peak sets, both when selected by human operators and when selected by automatic peak detection algorithms. This variation has been used as an advantage to gain significantly better protein identification results, using the Pepex tool, than what an experienced mass spectroscopist has achieved on the same data. The strongest improvement has been observed in weak spectra, where the signal peak intensities are low.