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Contains unique collection of genetically-modified mice that available for rederivation. All lines have been either generated or modified by Vanderbilt investigators, and are not available in any other repository.
Biomedical company specializing in cancer diagnosis. Research oriented company with competitive networking and marketing skills by forming mutually beneficial partnerships. Aims to lead the popularization of cancer screening by changing the paradigm of cancer diagnostics that allows cancer screening anywhere, anytime.
Provides comprehensive dataset based on National Health Insurance program, which has covered over 99% of Taiwan's population since its launch in 1995. Database includes anonymized data on outpatient and inpatient visits, prescriptions, surgeries, diagnostics, and other medical information, ensuring individual privacy protection. NHI database is extensively utilized in fields such as public health, epidemiology, drug safety, and chronic disease monitoring, providing critical insights for research on major health conditions like cancer and cardiovascular diseases. Researchers use the NHIRD for long-term follow-up studies, treatment outcome analyses, and identifying disease risk factors, making it a valuable resource for healthcare policy and medical decision-making.
Provides comprehensive national registry that systematically records all live births in Taiwan. It captures essential data on maternal and infant health, including maternal demographics, prenatal care, gestational age, birth weight, delivery method, and congenital anomalies. Established to facilitate public health monitoring and research, the TBRS enables studies on birth trends and outcomes, such as preterm birth and low birth weight, and provides a valuable resource for investigating the impacts of maternal health, environmental factors, and healthcare access on neonatal outcomes.TBRS database is instrumental in informing maternal and child health policies in Taiwan.
Platform brings together patients and caregivers, community groups, health system innovators and clinicians, and academic researchers to produce meaningful research and innovation that advances health and research outcomes.
Core provides investigators access to state-of-the-art vector technology for preclinical studies and other basic research applications.
Software to process non-targeted analyses from Bruker's ESI and MALDI imaging instruments. Supports workflows ranging from basic ID to advanced statistics.
Company specializing in antibody customization and antibody-related services. Develops functional antibodies and antibodies for detection of pharmaceutical targets and monoclonal antibodies with development time from six months to weeks.
Software tool to test for pleiotropic association between expression level of gene and complex trait of interest using summary-level data from GWAS and expression quantitative trait loci eQTL studies. Used to prioritize genes underlying GWAS hits for follow up functional studies.
Software package to perform genetic colocalisation analysis of two potentially related phenotypes, to ask whether they share common genetic causal variant(s) in a given region.Colocalisation Tests of Two Genetic Traits.
Software tool for genome-wide association study analysis, designed to perform range of basic and advanced meta-analytic methods.
High-performance, fully-automated, inverted, multi-channel fluorescence and transmitted light imaging system controlled by the integrated EVOS FL Auto software.
Function-based gut microbiome health index.
Provides access to various microscopes and services, support and training for fluorescence microscopy experiments and image analysis. Facility offers imaging tasks from basic neuron reconstruction to high-speed, deep-tissue optogenetic experiments in brain slices or live animals.
Slide scanner provides automation for small-to medium-volume labs looking to make the transition to digital pathology. Scanner offers walk-away scanning of up to 160 slides, and produces high-quality images and offers advanced slide handling.
Brain bank that houses donated brains from people with neurodegenerative diseases and neurologically normal age-matched controls. VAI Brain Bank drives insight and discovery by providing scientists the samples needed to investigate the intricate underpinnings of Parkinson’s, dementias, and other neurodegenerative diseases.
Microscope allows real-time fluorescence imaging of 3D tissue sections typically used in neuroscience and histology research. Acquire rich, detailed images of thick tissues, free from the haze of out-of-focus blur.
Software tool for multiparametric analysis of complex flow cytometry data. Compatible with FCS standard files .Offers features to enhance data integration, interpretation, and visualization. Users can create personalized analysis templates for different types of analyses, with no limit on the number of profiles or diagrams.
Software tool to discover somatic and germline structural variation breakpoints in whole genome sequencing data. Can report accurate breakpoints of Deletions, Duplications, Inversions and Translocations. Designed for Illumina paired-end data. Local assembly for breakpoint detection in cancer genomes.
Software tool as streamlined code editor with support for development operations like debugging, task running, and version control. Aims to provide just the tools developer needs for quick code-build-debug cycle.