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.

Wangcheng Wu

dblp:82/9109 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2011
—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 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › epigenomics
ChIP-chip analysis
0.112011
W-ChIPeaks: a comprehensive web application tool for processing ChIP-chip and ChIP-seq data · Bioinform. 2011
Bioinformatics and computational biology › epigenomics
ChIP-seq analysis
0.112011
W-ChIPeaks: a comprehensive web application tool for processing ChIP-chip and ChIP-seq data · Bioinform. 2011
Bioinformatics and computational biology › epigenomics › ChIP-seq analysis
peak calling
0.112011
W-ChIPeaks: a comprehensive web application tool for processing ChIP-chip and ChIP-seq data · Bioinform. 2011
Bioinformatics and computational biology › gene regulation
transcription factor binding site prediction
0.012011
W-ChIPeaks: a comprehensive web application tool for processing ChIP-chip and ChIP-seq data · Bioinform. 2011

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

statistical enrichment threshold · 0.1false discovery rate control · 0.1
YearPublicationVenuePosition
2011 W-ChIPeaks: a comprehensive web application tool for processing ChIP-chip and ChIP-seq data
abstract
UNLABELLED: ChIP-based technology is becoming the leading technology to globally profile thousands of transcription factors and elucidate the transcriptional regulation mechanisms in living cells. It has evolved rapidly in recent years, from hybridization with spotted or tiling microarray (ChIP-chip), to pair-end tag sequencing (ChIP-PET), to current massively parallel sequencing (ChIP-seq). Although there are many tools available for identifying binding sites (peaks) for ChIP-chip and ChIP-seq, few of them are available as easy-accessible online web tools for processing both ChIP-chip and ChIP-seq data for the ChIP-based user community. As such, we have developed a comprehensive web application tool for processing ChIP-chip and ChIP-seq data. Our web tool W-ChIPeaks employed a probe-based (or bin-based) enrichment threshold to define peaks and applied statistical methods to control false discovery rate for identified peaks. The web tool includes two different web interfaces: PELT for ChIP-chip, BELT for ChIP-seq, where both were tested on previously published experimental data. The novel features of our tool include a comprehensive output for identified peaks with GFF, BED, bedGraph and .wig formats, annotated genes to which these peaks are related, a graphical interpretation and visualization of the results via a user-friendly web interface. AVAILABILITY: http://motif.bmi.ohio-state.edu/W-ChIPeaks/.
Xun Lan, Russell Bonneville, Jeff Apostolos, Wangcheng Wu, Victor X. Jin
Bioinform.4