Demo Data from VLDB 2026 / reviewers in the wild / expert
Bret Cooper
dblp:25/6113
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2007
0000-0003-4915-2200ORCID · reported
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › protein structure prediction
decoy generation |
0.1 | 1 | 2007 | Probability-based pattern recognition and statistical framework for randomization: modeling tandem mass spectrum/peptide sequence false match frequencies · Bioinform. 2007 |
Bioinformatics and computational biology › proteomics
mass spectrometry data analysis |
0.1 | 1 | 2007 | Probability-based pattern recognition and statistical framework for randomization: modeling tandem mass spectrum/peptide sequence false match frequencies · Bioinform. 2007 |
Bioinformatics and computational biology
proteomics |
0.1 | 1 | 2007 | Probability-based pattern recognition and statistical framework for randomization: modeling tandem mass spectrum/peptide sequence false match frequencies · Bioinform. 2007 |
Methods — techniques the papers use, named apart from their topics
pattern recognition · 0.1monte carlo sampling · 0.1
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2007 | Probability-based pattern recognition and statistical framework for randomization: modeling tandem mass spectrum/peptide sequence false match frequenciesabstractMOTIVATION: In proteomics, reverse database searching is used to control the false match frequency for tandem mass spectrum/peptide sequence matches, but reversal creates sequences devoid of patterns that usually challenge database-search software. RESULTS: We designed an unsupervised pattern recognition algorithm for detecting patterns with various lengths from large sequence datasets. The patterns found in a protein sequence database were used to create decoy databases using a Monte Carlo sampling algorithm. Searching these decoy databases led to the prediction of false positive rates for spectrum/peptide sequence matches. We show examples where this method, independent of instrumentation, database-search software and samples, provides better estimation of false positive identification rates than a prevailing reverse database searching method. The pattern detection algorithm can also be used to analyze sequences for other purposes in biology or cryptology. AVAILABILITY: On request from the authors. SUPPLEMENTARY INFORMATION: http://bioinformatics.psb.ugent.be/. Daniel Q. Naiman, Bret Cooper |
Bioinform. | 3 |