Informatics research to enable clinically relevant, personalized genomic medicine
National centers for biomedical computing : from the BISTI report to the future
Translational informatics : an industry perspective
Advantages of genomic complexity : bioinformatics opportunities in microRNA cancer signatures
Reconciliation of the cloud computing model with US federal electronic health record regulations
The NIH National Center for Integrative Biomedical Informatics (NCIBI)
Using systems and structure biology tools to dissect cellular phenotypes
The National Alliance for Medical Image Computing, a roadmap initiative to build a free and open source software infrastructure for translational research in medical image analysis
A translational engine at the national scale : informatics for integrating biology and the bedside
Simbios : an NIH national center for physics-based simulation of biological structures
The National Center for Biomedical Ontology
iDASH : integrating data for analysis, anonymization, and sharing
The Center for Computational Biology : resources, achievements, and challenges
Utility of gene-specific algorithms for predicting pathogenicity of uncertain gene variants
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study
Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records
Exploiting domain information for Word Sense Disambiguation of medical documents
Identifying disease genes and module biomarkers by differential interactions
A vector space model approach to identify genetically related diseases
Predicting the outcome of renal transplantation
Calibrating predictive model estimates to support personalized medicine
Incorporating molecular and functional context into the analysis and prioritization of human variants associated with cancer
Multiplex meta-analysis of RNA expression to identify genes with variants associated with immune dysfunction
A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data
Complex-disease networks of trait-associated single-nucleotide polymorphisms (SNPs) unveiled by information theory
Translating Mendelian and complex inheritance of Alzheimer's disease genes for predicting unique personal genome variants
Integrated morphologic analysis for the identification and characterization of disease subtypes
President's column : reflections on AMIA's past 3 years