Sciweavers

378 search results - page 11 / 76
» Data integration and genomic medicine
Sort
View
NAR
2000
120views more  NAR 2000»
14 years 11 months ago
WIT: integrated system for high-throughput genome sequence analysis and metabolic reconstruction
The WIT (What Is There) (http://wit.mcs.anl.gov/WIT2/ ) system has been designed to support comparative analysis of sequenced genomes and to generate metabolic reconstructions bas...
Ross A. Overbeek, Niels Larsen, Gordon D. Pusch, M...
GI
2004
Springer
15 years 5 months ago
Dynamic information fusion for genome annotation
: The need for demand-driven and scaleable integration of heterogeneous data sources is inherent to the process of genome annotation. In this paper we describe the Gene-EYe archite...
Heiko Müller, Peter Rieger, Katja Tham, Johan...
BMCBI
2007
131views more  BMCBI 2007»
15 years 4 hour ago
FUNC: a package for detecting significant associations between gene sets and ontological annotations
Background: Genome-wide expression, sequence and association studies typically yield large sets of gene candidates, which must then be further analysed and interpreted. Informatio...
Kay Prüfer, Bjoern Muetzel, Hong Hai Do, Gunt...
PAKDD
2005
ACM
103views Data Mining» more  PAKDD 2005»
15 years 5 months ago
Subgroup Discovery Techniques and Applications
This paper presents the advances in subgroup discovery and the ways to use subgroup discovery to generate actionable knowledge for decision support. Actionable knowledge is explici...
Nada Lavrac
IPPS
2010
IEEE
14 years 9 months ago
pFANGS: Parallel high speed sequence mapping for Next Generation 454-roche Sequencing reads
Millions of DNA sequences (reads) are generated by Next Generation Sequencing machines everyday. There is a need for high performance algorithms to map these sequences to the refer...
Sanchit Misra, Ramanathan Narayanan, Wei-keng Liao...