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Xiangqun Zheng Bradley

dblp:09/7064 · also Xiangqun H. Zheng · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2009
0000-0002-9324-2708ORCID · verified

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
comparative genomics
0.112005
Using shared genomic synteny and shared protein functions to enhance the identification of orthologous gene pairs · Bioinform. 2005
Bioinformatics and computational biology › comparative genomics › orthology analysis
ortholog identification
0.112005
Using shared genomic synteny and shared protein functions to enhance the identification of orthologous gene pairs · Bioinform. 2005
Bioinformatics and computational biology
data mining
0.012009
MAGETabulator, a suite of tools to support the microarray data format MAGE-TAB · Bioinform. 2009
Bioinformatics and computational biology
genome annotation
0.012005
Using shared genomic synteny and shared protein functions to enhance the identification of orthologous gene pairs · Bioinform. 2005
Bioinformatics and computational biology
protein function prediction
0.012005
Using shared genomic synteny and shared protein functions to enhance the identification of orthologous gene pairs · Bioinform. 2005

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

sequence similarity · 0.1TBLASTX · 0.1
YearPublicationVenuePosition
2009 MAGETabulator, a suite of tools to support the microarray data format MAGE-TAB
abstract
Abstract Summary: The MAGE-TAB format for microarray data representation and exchange has been proposed by the microarray community to replace the more complex MAGE-ML format. We present a suite of tools to support MAGE-TAB generation and validation, conversion between existing formats for data exchange, visualization of the experiment designs encoded by MAGE-TAB documents and the mining of such documents for semantic content. Availability: Software is available from http://tab2mage.sourceforge.net/ Contact: [email protected]
Tim F. Rayner, Faisal Ibne Rezwan, Margus Lukk, Xiangqun Zheng Bradley, Anna Farne, Ele Holloway, James Malone, Eleanor Williams, Helen E. Parkinson
Bioinform.4
2005 Using shared genomic synteny and shared protein functions to enhance the identification of orthologous gene pairs
abstract
MOTIVATION: The identification of orthologous gene pairs is generally based on sequence similarity. Gene pairs that are mutually 'best hits' between the genomes being compared are asserted to be orthologs. Although this method identifies most orthologous gene pairs with high confidence, it will miss a fraction of them, especially genes in duplicated gene families. In addition, the approach depends heavily on the completeness and quality of gene annotation. When the gene sequences are not correctly represented the approach is unlikely to find the correct ortholog. To overcome these limitations, we have developed an approach to identify orthologous gene pairs using shared chromosomal synteny and the annotation of protein function. RESULTS: Assembled mouse and human genomes were used to identify the regions of conserved synteny between these genomes. 'Syntenic anchors' are conserved non-repetitive locations between mouse and human genomes. Using these anchors, we identified blocks of sequences that contain consistently ordered anchors between the two genomes (syntenic blocks). The synteny information has been used to help us identify orthologous gene pairs between mouse and human genomes. The approach combines the mutual selection of the best tBlastX hits between human and mouse transcripts, and inferring gene orthologous relationships based on sharing syntenic anchors, collocating in the same syntenic blocks and sharing the same annotated protein function. Using this approach, we were able to find 19,357 orthologous gene pairs between human and mouse genomes, a 20% increase in the number of orthologs identified by conventional approaches.
Xiangqun Zheng Bradley, Fu Lu, Zhen-Yuan Wang, Fei Zhong, Jeffrey Hoover, Richard J. Mural
Bioinform.1