Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Jiongtang Li

dblp:15/6885 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2016
—ORCID · none

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly
0.212016
PEP_scaffolder: using (homologous) proteins to scaffold genomes · Bioinform. 2016
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly
scaffolding
0.212016
PEP_scaffolder: using (homologous) proteins to scaffold genomes · Bioinform. 2016
Bioinformatics and computational biology
proteomics
0.112016
PEP_scaffolder: using (homologous) proteins to scaffold genomes · Bioinform. 2016

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

homologous protein alignment · 0.2
YearPublicationVenuePosition
2016 PEP_scaffolder: using (homologous) proteins to scaffold genomes
abstract
MOTIVATION: Recovering the gene structures is one of the important goals of genome assembly. In low-quality assemblies, and even some high-quality assemblies, certain gene regions are still incomplete; thus, novel scaffolding approaches are required to complete gene regions. RESULTS: We developed an efficient and fast genome scaffolding method called PEP_scaffolder, using proteins to scaffold genomes. The pipeline aims to recover protein-coding gene structures. We tested the method on human contigs; using human UniProt proteins as guides, the improvement on N50 size was 17% increase with an accuracy of ∼97%. PEP_scaffolder improved the proportion of fully covered proteins among all proteins, which was close to the proportion in the finished genome. The method provided a high accuracy of 91% using orthologs of distant species. Tested on simulated fly contigs, PEP_scaffolder outperformed other scaffolders, with the shortest running time and the highest accuracy. AVAILABILITY AND IMPLEMENTATION: The software is freely available at http://www.fishbrowser.org/software/PEP_scaffolder/ CONTACT: [email protected] information: Supplementary data are available at Bioinformatics online.
Bai-Han Zhu, Ying-Nan Song, Gui-Cai Xu, Ming-Yuan Sun, Xiaowen Sun, Jiongtang Li
Bioinform.8