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Andrew Campen

dblp:75/5170 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2008
—ORCID · none

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

Databases, data management, data science and information retrieval · 1 · 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
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis › molecular signature analysis
prognostic gene signature identification
0.112008
Mining Gene Expression Database for Primary Human Disease Tissues · ICDE 2008

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

statistical pipeline · 0.1gene signature analysis · 0.1
YearPublicationVenuePosition
2008 Mining Gene Expression Database for Primary Human Disease Tissues
abstract
Studies of gene expression in primary human disease tissue often span several years in order to achieve reasonably large sample sizes and to collect patient clinical information making this data particularly valuable. Due to the lack of a central repository, this data has only been available through disparate and non-publicly accessible sources following publication. We developed disease-to-gene expression mapper (D-GEM) as a publically accessible database and data mining toolbox for microarray data of human primary disease tissue. A statistical pipeline has also been implemented to identify genes over-expressed in disease tissue samples in comparison with normal control samples, or genes whose expression values are associated with clinical parameters such as patient survival rate. One potential application of this data is the identification of pathway specific cancer prognosis markers. By applying a novel, gene signatures for cancer prognosis in the context of known biological pathways in cancer development were identified and confirmed.
Andrew Campen, Yuni Xia, Dan Rigsby, Xingdong Feng, Eric W. Su, Mathew J. Palakal
ICDE1