We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms
The High-Performance Computing (HPC) Facility provides the hardware and staff to support bioinformatics and biocomputational research. The central component of this facility is a large cluster of 64 high-speed compute nodes, along with approximately 900 terabyte of shared disk storage and nearly 1.8 petabytes of archival storage.
Provides mouse genotyping service, from extraction of genomic DNA from tissue to reporting of genotypes. Offers Mycoplasma testing of any cell line and authentication of human cell lines.
A nonprofit medical teaching and training school in Memphis, Tennessee qualified under section 501 (c) (3) of the Internal Revenue Code. The MERI conducts state-of-the-art, hands-on educational courses for physicians, nurses and other medical professionals from across the country and around the world. At the MERI, medical professionals are introduced to the latest innovations in medicine, and have the opportunity to learn first-hand about the most up-to-date medical techniques and technologies. The MERI supports research in all specialties by providing the sponsor with the most effective environment for achieving maximal outcomes for their studies. Through our Mobile MERI unit, we are proud to provide courses and support to our sponsors off-site anywhere in the continental United States. Our dedicated course specialists offer customer service, provide safe and efficient transport of equipment and ensure a quality training and educational experience at the off-site location.
MaizeDIG is a genotype-phenotype database for maize images. MaizeDIG supports multiple reference genome assemblies, is seamlessly integrated with genome browsers to accommodate custom tracks showing tagged mutant phenotypes images in their genomic context, and allows for custom tagging of images to highlight the phenotypes. This is accomplished through an interface allowing users to create image-to-gene links and is accessible via search tools.
Core provides high throughput transcriptional profiling, genotyping, protein quantitation, protein profiling and identification, real-time PCR and robotics. Genomics core offers Affymetrix gene chip technologies, both cartridge based and 96 well high throughput, analysis of genomic information with as little as 50ng of RNA, RNA extracted from paraffin based samples, or partially degraded RNA. Proteomics services include design, performance and analysis of proteomic studies.
THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 22, 2022. Data set collected at the Children''s Hospital Boston, of EEG recordings from pediatric subjects with intractable seizures. Subjects were monitored for up to several days following withdrawal of anti-seizure medication in order to characterize their seizures and assess their candidacy for surgical intervention. All signals were sampled at 256 samples per second with 16-bit resolution. Most files contain 23 EEG signals (24 or 26 in a few cases).
UK’s national organization for the 3Rs (Replacement, Reduction and Refinement) to advance the 3Rs framework for performing more humane animal research by focusing on scientific impacts and benefits to better reflect contemporary scientific practice and developments.
Software R package for detecting rhythmic signals from large scale time-series data. Used to evaluate periodicity in large scale data.
UniProtKB entries are tagged with keywords that can be used to retrieve particular subsets of entries. There are 10 categories of keywords: Biological process Cellular component Coding sequence diversity Developmental stage Disease Domain Ligand Molecular function Post-translation modification Technical term You may browse by hierarchy, search in Keywords, or list all keywords. By default, searching the keywords will look for matches in both name and definition.
Software tool as open source programming language to build simple, reliable, and efficient software. Developed by team at Google and many contributors from open source community.
Software label transfer tool for single-cell RNA sequencing analysis. Scalable, Interpretable Modeling for Single-cell RNA-seq data classification.
Emergency Medicine is an Open-Content Textbook of Emergency Medicine. This wikibook is intended to be a collaborative communication between physicians, nurses, physician assistants, paramedics, EMTs and other healthcare providers. It is not intended for the general public. It is under development and inevitably contains many errors and omissions. As the information in this textbook can be edited by anyone, regardless of whether they are medically trained or not, it should not be used as a guide to treating yourself or anyone else! Contents * 1 SYMPTOMS AND PRESENTATIONS ** 1.1 GENERAL SYMPTOMS ** 1.2 HEAD AND NECK SYMPTOMS ** 1.3 CHEST SYMPTOMS ** 1.4 ABDOMINAL SYMPTOMS * 2 TOPICS ** 2.1 ABDOMINAL AND GASTROINTESTINAL DISORDERS ** 2.2 CARDIOVASCULAR DISORDERS ** 2.3 CUTANEOUS DISORDERS ** 2.4 DISASTER MEDICINE ** 2.5 ENDOCRINE, METABOLIC, AND NUTRITIONAL DISORDERS ** 2.6 ENVIRONMENTAL DISORDERS ** 2.7 HEAD, EAR, EYE, NOSE, THROAT DISORDERS ** 2.8 HEMATOLOGIC DISORDERS ** 2.9 IMMUNE SYSTEM DISORDERS ** 2.10 INFECTIOUS DISORDERS ** 2.11 MUSCULOSKELETAL DISORDERS (NONTRAUMATIC) ** 2.12 NERVOUS SYSTEM DISORDERS ** 2.13 OBSTETRICS AND GYNECOLOGY ** 2.14 RENAL AND UROGENITAL DISORDERS ** 2.15 THORACIC-RESPIRATORY DISORDERS ** 2.16 TOXICOLOGIC DISORDERS ** 2.17 TRAUMATIC DISORDERS * 3 TESTS ** 3.1 Imaging ** 3.2 Lab Investigations ** 3.3 Point of Care Testing * 4 TREATMENT ** 4.1 Procedures ** 4.2 Resuscitation ** 4.3 Other Treatment * 5 SPECIAL POPULATIONS * 6 PRACTICE AND ADMINISTRATION * 7 KNOWLEDGE AND COMMUNICATION
anti-Oct4 (3F5) Mouse mAb is antibody from Zen bioscience in China for research use only.
Software R package as global weighted model for disease ontology enrichment analysis. Used for annotating and enrichment analysis with disease ontology.
THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 11, 2023. A private repository of clinical and genetic information on families with autism. Genetic and clinical data are obtained from families that have more than one family member diagnosed with an Autism Spectrum Disorder. The biological samples, along with the accompanying clinical data, are made available to AGRE-approved researchers worldwide. As they become available, additional family pedigrees will be posted in the online catalog. Cell lines have been established for the majority of families in this collection and serum/plasma is available on a subset of the subjects until stocks are depleted. The diagnosis of autism has been made using the standard Autism Diagnostic Interview-Revised (ADI-R) algorithm and the Autism Diagnostic Observation Scale (ADOS-G). Detailed birth and medical histories (including basic dysmorphology assessments) on children as well as family and medical information for parents and unaffected siblings, are available for nearly all families. DNA, cell lines, serum, plasma and clinical information are made available to AGRE-approved researchers for analysis.
Software Python tool as viewer for MRI data and numpy arrays.
Software R package for DNA copy number detection from off-target sequence data. Used to extract DNA copy number information from targeted sequencing by utiizing off-target reads.
The Guthy-Jackson Charitable Foundation is dedicated to funding basic science research to find answers that will lead to the prevention, clinical treatment programs and a potential cure for Neuromyelitis Optica (NMO) Spectrum Disease. The decision to create our Foundation came from a personal family crisis. Our daughter was officially diagnosed with NMO in June 2008. Since that time, we have met with many clinicians and researchers in order to understand what this means for our beautiful daughter and our family. Additionally, we have gathered and read every piece of information and NMO research article that is available on the Web. We are now beginning to understand that NMO is not only considered an orphan disease, but that very little research is available. We met with the All Greater Good Foundation in early July 2008 when it became clear that there is little-to-no funding available to research this rare and often misunderstood disease. We joined hands with the All Greater Good Foundation to immediately begin our work, and thus, The Guthy-Jackson Charitable Foundation was born. The Guthy-Jackson Charitable Foundation is dedicated to funding biomedical research in the search to understand the pathophysiology and biochemistry of NMO Spectrum Disease. It is our greatest hope that together we will reverse the effects of NMO and eventually cure this disease.
BossDB (Brain Observatory Storage Service and Database) is a cloud-based ecosystem for the storage and management of public large-scale volumetric neuroimaging and connectomics datasets. This includes volumetric Electron Microscopy and X-Ray Micro/Nanotomography data with support for multi-channel image data, segmentations, annotations, meshes, and connectomes. BossDB integrates with community resources for data access, processing, visualization, and analysis, and includes an API that enables metadata management, rendering, datatype conversions, and ingest.
Software R package as collection of useful utility functions from Seminar for Statistics (SfS) at ETH Zurich.