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Hong Li 0013

dblp:93/6234-13 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2016
—ORCID · conflict

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis › gene expression quantification
allele-specific expression
0.212016
cisASE: a likelihood-based method for detecting putative cis-regulated allele-specific expression in RNA sequencing data · Bioinform. 2016
Bioinformatics and computational biology › proteomics › computational proteomics
proteome annotation
0.112009
PAnnBuilder: an R package for assembling proteomic annotation data · Bioinform. 2009
Bioinformatics and computational biology › transcriptomics
RNA-seq analysis
0.112016
cisASE: a likelihood-based method for detecting putative cis-regulated allele-specific expression in RNA sequencing data · Bioinform. 2016

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

likelihood-based inference · 0.2DNA-seq bias correction · 0.2
YearPublicationVenuePosition
2016 cisASE: a likelihood-based method for detecting putative cis-regulated allele-specific expression in RNA sequencing data
abstract
MOTIVATION: Allele-specific expression (ASE) is a useful way to identify cis-acting regulatory variation, which provides opportunities to develop new therapeutic strategies that activate beneficial alleles or silence mutated alleles at specific loci. However, multiple problems hinder the identification of ASE in next-generation sequencing (NGS) data. RESULTS: We developed cisASE, a likelihood-based method for detecting ASE on single nucleotide variant (SNV), exon and gene levels from sequencing data without requiring phasing or parental information. cisASE uses matched DNA-seq data to control technical bias and copy number variation (CNV) in putative cis-regulated ASE identification. Compared with state-of-the-art methods, cisASE exhibits significantly increased accuracy and speed. cisASE works moderately well for datasets without DNA-seq and thus is widely applicable. By applying cisASE to real datasets, we identified specific ASE characteristics in normal and cancer tissues, thus indicating that cisASE has potential for wide applications in cancer genomics. AVAILABILITY AND IMPLEMENTATION: cisASE is freely available at http://lifecenter.sgst.cn/cisASE CONTACT: [email protected] or [email protected] information: Supplementary data are available at Bioinformatics online.
Tuantuan Gui, Hong Li 0013, Yunhe Fu
Bioinform.4
2009 PAnnBuilder: an R package for assembling proteomic annotation data
abstract
Abstract Summary: PAnnBuilder is an R package to automatically assemble protein annotation information from public resources to provide uniform annotation data for large-scale proteomic studies. Sixteen public databases have been parsed and 54 annotation packages have been constructed based on R environment or SQLite database. These ready-to-use packages cover most frequently needed protein annotation for three model species including human, mouse and rat. Several extended applications such as annotation based on protein sequence similarity are also provided. Sophisticated users can develop their own packages using PAnnBuilder. PAnnBuilder may become an important tool for proteomic research. Availability: PAnnBuilder and example annotation packages are freely available from http://www.biosino.org/PAnnBuilder/ Contact: [email protected]; [email protected]
Hong Li 0013, Guohui Ding 0001, Lu Xie
Bioinform.1