Pharmacy fill data as an indicator of patient adherence

Network Visualization and Analysis of Pregnant Uterine Contractions

How Circos Ideograms Complement Networks: A Case Study in Asthma

Linking Genotype to Phenotype: A Pilot Project to Create a Research Data Warehouse of Biospecimen and "Omic" Information

Developing an Ontology-driven Data Collection Application

Cancer Informatics Services: an infrastructure for translational cancer biomarker studies

A novel bioinformatics framework to explore the existing possibility of new drug target proteins in the human Malaria parasite

Protein-Network Modeling of Prostate Cancer Gene Signatures Reveals Essential Pathways in Disease Recurrence

Genome-Wide Methylation Analysis of CpG Island Methylator Phenotype Cancers

Proposed Agent-directed Composition of Biomedical and Simulation Ontologies: Facilitating Dynamic Hypothesis Instantiation

Modeling the Expansion of Cancer Registry Services Across Distributed Grid Computer Systems Using a Sampling Based Approach

Drug-Gene Retriever: An unsupervised system to identify drug-gene relationships

MOUSER: An Online Mouse Registry for Biomedical Researchers

Toward an automatic method for extracting cancer- and other disease-related point mutations from the biomedical literature

FunDO: A Web Tool Exploring Genes Using Functional Disease Ontology Annotations

Discovering biomedical research resources in text: an ontology-driven approach using curated data for incremental retraining

Designing Effective Clinical Trials Using Simulations

Managing Variability in Co-Expression Network Construction

Paradigm Integrated Pathway Analysis of Drug Subtype Sensitivity (DSS)

A Metamodel for Collaborative Sharing of Biomedical Research Experiments

Finding Text in Scientific Publications Relevant to Phenotypic Concepts

Differential Expression Analysis for Pathways

Mining and Visualization of Pain Descriptors from Clinical Records – A Pilot Study

PheGenI: an Integrated Resource for Browsing Genetic Association Data

The FaceBase Management and Coordination Hub: Development and Design Principles for a Translational BioInformatics Data Portal

Discovering Disease Associaciations by Integrating Electronic Health Records and Medical Literature

Gene Signature identified by Tissue-Decomposition Predicts Response To Preoperative Chemotherapy

The PhenX Toolkit: Toward Data Interoperability for Genome Wide Association Studies

Using Circulating Plasma Protein Biomarkers of Inflammation and Vascular Modeling to Detect Abdominal Aortic Aneurysm

OAMiner: An Application of Hypothesis Discovery within the Osteoarthritis Domain

The Human Variome Project: A Network of Scientists and Tools Constructed with the Goal of Understanding and Treating Genetic Diseases

Annotation of disease-associated SNPs with eQTLs to elucidate mechanisms of disease

Clustering of Human Diseases and Genetic and Environmental Factors

Understanding variable representation for causal inference in EHRs

International, Interoperable, Harmonized Systems for Integrating Multi-omic Data Sources to Characterize and Quantify Metabolic and Nutritional Phenotypes

Semantic Web Methodologies Provide Access to FLU Data Without Getting You Sick of Searching

Capturing Structured Gene Variant Data using GVF, XML and HL7

Novel method for identification of chromosomal gain loci from conventional gene expression arrays

Uncovering genes associated with human infections in pathogenic bacteria: a novel integrative analysis linking genome, bibliome, and diseasome

Stratification of Osteoarthritis Patients by Molecular Profiling Analysis of Synovium Tissue

Predicting Colorectal Cancer Patients' Survivability: The Comparison of Using Three Data Mining Methods- Artificial Neural Network, Logistic Regression and Decision Tree

The University of California at Santa Cruz- University of California at San Francisco Prostate Cancer Genomics Browser

Revealing signaling modules in cancers by mining TCGA data with integrated data-mining and knowledge-mining

Institutional Architecture for Secondary Data Use

Translational Informatics To Link Gene Activity To Ontologies With And Without Context

Conceptual Models for Interoperability in caBIG Using the Semantic Web

A Practical Approach to Automated OWL Annotation

Linking Model Organisms and Resources to Human Diseases using an Ontology-based Approach

Imaging Genetics: Replication of APOE, PICALM, and BIN1 Associations with Alzheimer Disease

Acquiring Biomedical Ontologies from Spreadsheets

Extending i2b2 for Cancer Research: Adding Episode and Somatic Mutations

Supporting Disease Ontology Refinement and Query Accuracy through a Cohort Identification Interface

Using Density Estimates to Aggregate Patients and Summarize Disease Evolution

Informatics System with Imaging and Touchscreen Devices for Duchenne Muscular Dystrophy Multicenter Clinical Trial

Use of Supervised and Unsupervised Machine Learning Algorithms to Identify Subtypes in Subjects with Post Traumatic Stress Disorder

Translating Ethnopharmacological Findings into Novel Drug Leads: the Potential Roles of Linked Open Data and Ontologies

Using Ontologies to Integrate Phenotype Measurement Values for Multiple Disease Models

Sigmoid Weighted ReliefF (SWRF) for Ranking SNPs

Genome-wide Association Study of Personality Disorder in Adults with Attention-Deficit Hyperactivity Disorder

ACCF/AHA Key Data Elements and Definitions of a Base Cardiovascular Vocabulary for Electronic Health Records

Activities of the Sage Bionetworks Working Group on Data Standards and Annotations

VIVO: Support for Translational Research

Distributed Infrastructure for Biomolecular Simulation-Derived Data Sharing and Analysis

The Regulation of Smoking on Airway Epithelial Gene Expression and a Detection Model for Smoking History

Biositemaps: A Framework for Biomedical Resource Discovery

Using OpenSocial to Build a Shareable Library of Research Applications

Integrative analysis identifies a novel regulator of colorectal cancer invasion

Computational Discovery of Dual-Function Biomarkers in Proteomics

Genetic Risk-variants Target FoxA1 Genomic Activity