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. 2007 Aug 31;8:323. doi: 10.1186/1471-2105-8-323

Table 1.

Comparison of the performance of conventional criteria, PeptideProphet and SFOER in peptide identifications for the analysis of human liver tissue lysatea

Conventional criteriab PeptideProphetc SFOERd
# 1+ 99 26 162
# 2+ 17950 17451 18606
# 3+ 7388 12587 11313
# total 25428 30064 30081
%incr / 18.2% 18.3%
# false pep 126 113 147
FDR 0.99% 0.75% 0.98%
#unique pep 4591 5175 5285
%incr unique pep / 12.7% 15.12%
# proteins 1467 1596 1665

a. Summary of each category returned by different strategies: #1+, #2+ and #3+ indicates the number of peptide identifications for charge states of 1+, 2+ and 3+ respectively. #total = (#1+) + (#2+) + (#3+). #false pep indicates the number of peptides from reversed database, while #unique pep is the number of total unique peptides. Increase of peptide identifications (%incr) and unique peptide identifications (%incr unique pep) by SFOER and PeptideProphet are shown. #proteins are the number of positive proteins identified by the strategies. FDR of identifications are also shown.

b. Conventional criteria. Xcorr > 2.0, 2.5 and 3.8 for singly, doubly and triply charged peptides, respectively and ΔCn > 0.164 for all charge states [25, 33].

c. Cutoff is set as PeptideProphet probability > 0.9 [13, 36-38].

d. Optimized criteria determined by SFOER are: according to the charge states of 1+, 2+ and 3+, Xcorr scores > 1.76, 2.31 and 2.41, ΔCn > 0.061, 0.199 and 0.265, Sp > 44.42, 104 and 276.9 and Rsp < 3, 4 and 2.