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Jinchao Yu

dblp:172/0121 · DBLP profile ↗
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2ranked-venue papers
2as first author
0since 2021 · last 2016
0000-0002-5431-8298ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein structure prediction
protein-protein docking
0.212016
PPI4DOCK: large scale assessment of the use of homology models in free docking over more than 1000 realistic targets · Bioinform. 2016
Bioinformatics and computational biology
structural bioinformatics
0.212016
PPI4DOCK: large scale assessment of the use of homology models in free docking over more than 1000 realistic targets · Bioinform. 2016
Bioinformatics and computational biology › multiple sequence alignment
profile hidden markov model alignment
0.212015
HHalign-Kbest: exploring sub-optimal alignments for remote homology comparative modeling · Bioinform. 2015
Bioinformatics and computational biology
protein structure prediction
0.212015
HHalign-Kbest: exploring sub-optimal alignments for remote homology comparative modeling · Bioinform. 2015
Bioinformatics and computational biology
sequence alignment
0.212015
HHalign-Kbest: exploring sub-optimal alignments for remote homology comparative modeling · Bioinform. 2015
Bioinformatics and computational biology › protein structure prediction
template-based modeling
0.212015
HHalign-Kbest: exploring sub-optimal alignments for remote homology comparative modeling · Bioinform. 2015

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

rigid-body docking · 0.2ZDOCK · 0.2hidden markov model · 0.2dynamic programming · 0.2directed acyclic graph · 0.2
YearPublicationVenuePosition
2016 PPI4DOCK: large scale assessment of the use of homology models in free docking over more than 1000 realistic targets
abstract
MOTIVATION: Protein-protein docking methods are of great importance for understanding interactomes at the structural level. It has become increasingly appealing to use not only experimental structures but also homology models of unbound subunits as input for docking simulations. So far we are missing a large scale assessment of the success of rigid-body free docking methods on homology models. RESULTS: We explored how we could benefit from comparative modelling of unbound subunits to expand docking benchmark datasets. Starting from a collection of 3157 non-redundant, high X-ray resolution heterodimers, we developed the PPI4DOCK benchmark containing 1417 docking targets based on unbound homology models. Rigid-body docking by Zdock showed that for 1208 cases (85.2%), at least one correct decoy was generated, emphasizing the efficiency of rigid-body docking in generating correct assemblies. Overall, the PPI4DOCK benchmark contains a large set of realistic cases and provides new ground for assessing docking and scoring methodologies. AVAILABILITY AND IMPLEMENTATION: Benchmark sets can be downloaded from http://biodev.cea.fr/interevol/ppi4dock/ CONTACT: [email protected] information: Supplementary data are available at Bioinformatics online.
Jinchao Yu, Raphaël Guérois
Bioinform.1
2015 HHalign-Kbest: exploring sub-optimal alignments for remote homology comparative modeling
abstract
MOTIVATION: The HHsearch algorithm, implementing a hidden Markov model (HMM)-HMM alignment method, has shown excellent alignment performance in the so-called twilight zone (target-template sequence identity with ∼20%). However, an optimal alignment by HHsearch may contain small to large errors, leading to poor structure prediction if these errors are located in important structural elements. RESULTS: HHalign-Kbest server runs a full pipeline, from the generation of suboptimal HMM-HMM alignments to the evaluation of the best structural models. In the HHsearch framework, it implements a novel algorithm capable of generating k-best HMM-HMM suboptimal alignments rather than only the optimal one. For large proteins, a directed acyclic graph-based implementation reduces drastically the memory usage. Improved alignments were systematically generated among the top k suboptimal alignments. To recognize them, corresponding structural models were systematically generated and evaluated with Qmean score. The method was benchmarked over 420 targets from the SCOP30 database. In the range of HHsearch probability of 20-99%, average quality of the models (TM-score) raised by 4.1-16.3% and 8.0-21.0% considering the top 1 and top 10 best models, respectively. AVAILABILITY AND IMPLEMENTATION: http://bioserv.rpbs.univ-paris-diderot.fr/services/HHalign-Kbest/ (source code and server). CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jinchao Yu, Géraldine Picord, Pierre Tufféry, Raphaël Guérois
Bioinform.1