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Lili Wang 0005

dblp:23/5672-5 · DBLP profile ↗
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2ranked-venue papers
2as first author
0since 2021 · last 2015
—ORCID · conflict

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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics › computational genomics
gene prioritization
0.212015
PINBPA: Cytoscape app for network analysis of GWAS data · Bioinform. 2015
Bioinformatics and computational biology › genomics
genome-wide association study
0.212015
PINBPA: Cytoscape app for network analysis of GWAS data · Bioinform. 2015
Bioinformatics and computational biology › systems bioinformatics › pathway analysis
network-based pathway analysis
0.212015
PINBPA: Cytoscape app for network analysis of GWAS data · Bioinform. 2015

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

subnetwork enrichment · 0.2random walk with restart · 0.2
YearPublicationVenuePosition
2015 PINBPA: Cytoscape app for network analysis of GWAS data
abstract
UNLABELLED: Protein interaction network-based pathway analysis (PINBPA) for genome-wide association studies (GWAS) has been developed as a Cytoscape app, to enable analysis of GWAS data in a network fashion. Users can easily import GWAS summary-level data, draw Manhattan plots, define blocks, prioritize genes with random walk with restart, detect enriched subnetworks and test the significance of subnetworks via a user-friendly interface. AVAILABILITY AND IMPLEMENTATION: PINBPA app is freely available in Cytoscape app store. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Lili Wang 0005, Takuya Matsushita, Lohith Madireddy, Parvin Mousavi, Sergio Baranzini
Bioinform.1
2011 iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
abstract
BACKGROUND: The speed at which biological datasets are being accumulated stands in contrast to our ability to integrate them meaningfully. Large-scale biological databases containing datasets of genes, proteins, cells, organs, and diseases are being created but they are not connected. Integration of these vast but heterogeneous sources of information will allow the systematic and comprehensive analysis of molecular and clinical datasets, spanning hundreds of dimensions and thousands of individuals. This integration is essential to capitalize on the value of current and future molecular- and cellular-level data on humans to gain novel insights about health and disease. RESULTS: We describe a new open-source Cytoscape plugin named iCTNet (integrated Complex Traits Networks). iCTNet integrates several data sources to allow automated and systematic creation of networks with up to five layers of omics information: phenotype-SNP association, protein-protein interaction, disease-tissue, tissue-gene, and drug-gene relationships. It facilitates the generation of general or specific network views with diverse options for more than 200 diseases. Built-in tools are provided to prioritize candidate genes and create modules of specific phenotypes. CONCLUSIONS: iCTNet provides a user-friendly interface to search, integrate, visualize, and analyze genome-scale biological networks for human complex traits. We argue this tool is a key instrument that facilitates systematic integration of disparate large-scale data through network visualization, ultimately allowing the identification of disease similarities and the design of novel therapeutic approaches.The online database and Cytoscape plugin are freely available for academic use at: http://www.cs.queensu.ca/ictnet.
Lili Wang 0005, Pouya Khankhanian, Sergio Baranzini, Parvin Mousavi
BMC Bioinform.1