14th SPGH Meeting
14th Portuguese Human Genetics Society annual meeting Coimbra, Portugal GEN2PHEN Project Open publication - Free publishing - More wave An Integrated View for the Human Variome Open publication - Free publishing - More wave Read More
An Integrated View for the Human Variome
Pedro Lopes and José Luís Oliveira 14th Annual Meeting of Portuguese Society for Human Genetics (SPGH 2010) Coimbra, Portugal; November 2010 Read More
An extensible platform for variome data integration
Pedro Lopes and José Luís Oliveira 10th IEEE International Conference on Information Technology and Applications in Biomedicine (ITAB 2010) Corfu, Greece, November 2010 Read More
ITAB2010
WAVe and ABC4Bio at International Conference on Information Technology and Applications in Biomedicine. An Extensible Platform for Variome Data Integration Open publication - Free publishing - More genetics A Tagging System for Bioinformatics Resources Open publication - Free publishing - More bioinformatics Read More
JBI2010
Another WAVe presentation at Jornadas de Bioinformatica 2010. A Holistic Approach for Integrating Genomic Variation Information Open publication - Free publishing - More genetics JBI2010 Read More
A Holistic Approach for Integrating Genomic Variation Information
Pedro Lopes and José Luís Oliveira 10th Spanish Symposium on Bioinformatics (JBI2010) Malaga, Spain, October 2010 Read More
WAVe & Semantic Web @ GEN2PHEN GAM6
GEN2PHEN GAM 6 September 27th, 2010, Montpellier WAVe Open publication - Free publishing - More bioinformatics Open publication - Free publishing - More semantic web Read More
An Integrated View for Human Variome Information
Pedro Lopes and José Luís Oliveira 14th International Conference on Research in Computational Molecular Biology (RECOMB2010) Lisbon, Portugal, August 2010 Read More
WAVe
2010 begun with a new challenge: plan and develop, as fast as possible, a simple variant integration application based on DiseaseCard‘s navigation concept. The idea was to reach GEN2PHEN‘s goals with a new DiseaseCard-like application focused on integrating LSDBs (no one does it!) and variants contained in those LSDBs. Moreover, relevant gene-related information (pathways, proteins…) should be provided in the elegant navigation... Read More