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Chenghua Tao

dblp:394/4477 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis
database search
0.812024
SpecEncoder: deep metric learning for accurate peptide identification in proteomics · Bioinform. 2024
Bioinformatics and computational biology › proteomics
peptide identification
0.812024
SpecEncoder: deep metric learning for accurate peptide identification in proteomics · Bioinform. 2024
Bioinformatics and computational biology
proteomics
0.812024
SpecEncoder: deep metric learning for accurate peptide identification in proteomics · Bioinform. 2024
Bioinformatics and computational biology › proteomics › mass spectrometry data analysis
spectral library search
0.812024
SpecEncoder: deep metric learning for accurate peptide identification in proteomics · Bioinform. 2024

Methods — techniques the papers use, named apart from their topics

tandem mass spectrometry · 0.8embedding · 0.8deep metric learning · 0.8
YearPublicationVenuePosition
2024 SpecEncoder: deep metric learning for accurate peptide identification in proteomics
abstract
MOTIVATION: Tandem mass spectrometry (MS/MS) is a crucial technology for large-scale proteomic analysis. The protein database search or the spectral library search are commonly used for peptide identification from MS/MS spectra, which, however, may face challenges due to experimental variations between replicated spectra and similar fragmentation patterns among distinct peptides. To address this challenge, we present SpecEncoder, a deep metric learning approach to address these challenges by transforming MS/MS spectra into robust and sensitive embedding vectors in a latent space. The SpecEncoder model can also embed predicted MS/MS spectra of peptides, enabling a hybrid search approach that combines spectral library and protein database searches for peptide identification. RESULTS: We evaluated SpecEncoder on three large human proteomics datasets, and the results showed a consistent improvement in peptide identification. For spectral library search, SpecEncoder identifies 1%-2% more unique peptides (and PSMs) than SpectraST. For protein database search, it identifies 6%-15% more unique peptides than MSGF+ enhanced by Percolator, Furthermore, SpecEncoder identified 6%-12% additional unique peptides when utilizing a combined library of experimental and predicted spectra. SpecEncoder can also identify more peptides when compared to deep-learning enhanced methods (MSFragger boosted by MSBooster). These results demonstrate SpecEncoder's potential to enhance peptide identification for proteomic data analyses. AVAILABILITY AND IMPLEMENTATION: The source code and scripts for SpecEncoder and peptide identification are available on GitHub at https://github.com/lkytal/SpecEncoder. Contact: [email protected].
Chenghua Tao, Yuzhen Ye, Haixu Tang
Bioinform.2