Curator Dashboard

Database integrating collagen biological and physicochemical properties with known variants. Web-based, interactive, graphical user interface displays data as annotations on collagen protein sequences. Collagen gene-level data are provided as custom tracks for display in the UCSC genome browser. COLdb currently includes 35,582 data points spanning collagen types I, II, and III, and, importantly, users can add their own data to the display. The database is the first comprehensive integration of disparate functional information on the three major fibrillar collagens, and the first electronic collection of mutations in the COL2A1 gene. Sponsors: This data base is supported by University of Leicester.

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• SciCrunch
• 17 years ago - by Anonymous

School of Pharmacy at North Dakota State University with mission of educating future pharmacists and researchers.

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• SciCrunch
• 17 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE.Documented on Januray 30,2023. NIH funded national research resource to provide biomedical research community with access to US born, known age, pedigreed, genomically sequenced, pathogen free Caribbean origin vervet monkeys also known as African green monkeys. Provides access to animals, extensive multisystem clinical phenotyping, sample and data repositories, expertise in use of nonhuman primate models for translational studies, serves as platform for training veterinarians and other professionals in biomedical research, husbandry, clinical care, and the colony behavioral management.

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• SciCrunch
• 17 years ago - by Anonymous

Genome Center uses technologies to understand how heritable genetic information of diverse organisms functions in health and disease. Provides research facilities, service cores, and staff for genomics research and training. Core facilities for Bioinformatics,DNA Technologies and Expression Analysis, Metabolomics, Proteomics,TILLING Core,Yeast One Hybrid Services Core.

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• SciCrunch
• 13 years ago - by Anonymous

Services offered include Human cell line authentication: Accurate validation of human cell lines using STR analysis and meeting the ANSI/ATCC requirements; Fragment analysis: Detection of changes in length of specific DNA sequence to indicate presence or absence of genetic marker; Oligo synthesis: Creation of custom primers and probes for oligo and siRNA synthesis through Integrated DNA Technologies (IDT); DNA quantification: Quantification, size and quality assessment of DNA samples; Consulting: For project design and sample preparation assistance.

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• SciCrunch
• 13 years ago - by Anonymous

THIS RESOURCE IS A DUPLICATE AND IS BEING REMOVED. A fee-for-service core facility that provides services and supervision in Transmission Electron Microscopy.

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• SciCrunch
• 13 years ago - by Anonymous

An Portal, Core facility.

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• SciCrunch
• 13 years ago - by Anonymous

Core provides range of services related to genome, epigenome, and transcriptome analysis. Offers technologies including Illumina deep sequencing and sample preparation for variety of applications, including DNA and RNA sequencing (DNA- and RNA-seq), exome sequencing, targeted capture, chromatin immunoprecipitation sequencing (ChIP-seq), methylation sequencing (Methyl-seq), metagenomics, and many others;Automation of Illumina library and targeted capture preps, including 16S ribosomal RNA (rRNA) sequencing;Oxford Nanopore sequencing (long reads);Bio-Rad Droplet Digita polymerase chain reaction (PCR);Nanostring nCounter;Single-cell RNA- and DNA-seq using the C1 Auto Prep System from Fluidigm, and 10x Genomics Chromium System.Provides expertise on strategies to achieve research goals in any field related to genomics, and can tailor bioinformatics analysis to individual project. If you supply us with nucleic acids, we can perform every step required to help you achieve your desired results.

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• SciCrunch
• 13 years ago - by Anonymous

The BIDMC Genomics and Proteomics Center provides all of the tools of modern functional genomics and proteomics, for academic and corporate clients alike. Equipped with State-of-the-Art technologies for high throughput transcriptional profiling, genotyping, protein quantitation, protein profiling and identification, real-time PCR and robotics. Located on the Harvard Medical School Longwood Campus. The BIDMC Genomics and Proteomics center is a core proteomics facility for the Dana-Farber/Harvard Cancer Center.

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• SciCrunch
• 13 years ago - by Anonymous

Browser to interactively visualize genomic data. Provides reference sequences and working draft assemblies for large collection of genomes and access to ENCODE and Neanderthal projects.

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• SciCrunch
• 13 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on April 23,2024. SMBC is resource of the Clinical and Translational Science Institute. Our services will provide quantitative analysis in clinical samples, with or without sample processing, using state-of-the-art instrumentation such as UPLC/MS/MS. The highly sensitive and specific techniques employed will allow the clinician to accurately measure multiple biomarkers in the same sample, maximizing the ability to link basic science with clinical outcomes.

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• SciCrunch
• 13 years ago - by Anonymous

Provided core services include Sanger DNA Sequencing, Next Generation DNA Sequencing (Four Illumina MiSeqs, four Illumina NextSeq 500s and one Illumina NovaSeq 6000),Next Generation Automated Library Sample Prep (Perkin Elmer Sciclone Genomic, ChIP, RNAseq and other methods), Single Cell DNA and RNA-Seq (10X Genomics Chromium), Bioanalyzer Analysis DNA and RNA (Two Agilent 2100 BioAnalyzers and two Agilent 2200 TapeStations), Qiagen Qiacube Automated DNA / RNA Prep (single to multiple samples), Oligonucleotide Ordering (IDT Portal), Reagents and Supplies Ordering (multiple vendors / products). Facility web based Laboratory Information Management System (LIMS) provides users with access to order services and supplies as well as retrieve data and review and pay invoices all online.

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• SciCrunch
• 13 years ago - by Anonymous

Core facility that provides the following services: Whole blood processing service, Cell surface staining, Cell subset enrichment service, Flow cytometry service, ELISPOT service, CFSE lymphoproliferation analysis service, Regulatory T cell conversion service, Multi-plex cytokine assay service, Flow cytometry assay service, Cell separation service. They are committed to assisting at all stages in the scientific process - from experimental design to data analysis - to meet the needs of faculty and other investigators. <BR/><BR/>DartLab is a Shared Resource that is used both by basic scientists and by clinicians carrying out mechanistic studies for clinical trials. Services are also available to non-Dartmouth clients. The consolidated Shared Resource moves beyond the simple provisioning of technical services to making complex experiments possible by providing scientific and technological support for implementing advanced, high-complexity assays in a cost-effective way, and by providing a mechanism for the acquisition of new methodologies. They carry out a spectrum of immunoassays and can develop customized immunoassays to suit your studies. They provide dedicated instruments for your use including cell sorters, flow cytometers, an ELISPOT reader, a Bio-Plex array reader and a Sector Imager, an autoMACS and a Robosep. Whole Blood Services * Flow Cytometry * Whole blood processing * Cell Subset Enrichment * Education * Clinical Trial Studies

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• SciCrunch
• 13 years ago - by Anonymous

More than 40 research scientists and engineers from diverse disciplines work together at the MNTC Center at the University of Louisville. Scientists with specialties in MEMS, bioMEMS, nanotechnology, electrooptics, biomechanics, bioengineering, microfabrication, and theoretical and applied physics, work along side scientists from the College of Arts and Sciences with expertise in molecular, cellular and structural biology and medicinal and combinatorial chemistry, and with cancer and genetic researchers from the Schools of Medicine and Dentistry.

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• SciCrunch
• 13 years ago - by Anonymous

Software package for working with VCF files. Used to provide easily accessible methods for working with complex genetic variation data in the form of VCF files.Implements various utilities for processing Variant Call Format files, including validation, merging, comparing. Provides general Perl API.

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• SciCrunch
• 12 years ago - by Anonymous

Complete guide to antibody research and suppliers. Serving the scientific community since 1997, the Antibody Resource Page is a guide designed by scientists for scientists to find companies that sell catalog antibodies and custom monoclonal and polyclonal antibodies. See our other pages on antibody-related databases, software, and educational websites. If you wish to suggest or update a link, please see our FAQ.

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• SciCrunch
• 13 years ago - by Anonymous

An open source software package for comparison and analysis of microbial communities, primarily based on high-throughput amplicon sequencing data, but also supporting analysis of other types of data.

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• SciCrunch
• 13 years ago - by Anonymous

THIS RESOURCE IS NO LONGER IN SERVICE, documented May 26, 2016; however, the URL provides links to associated projects and data. A suite of data query, download, upload, analysis and sharing tools serving the needs of the microbial ecology research community, and other scientists using metagenomics data.

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• SciCrunch
• 13 years ago - by Anonymous

Software for genomic expression data mining using a statistical technique for finding significant genes in a set of microarray experiments.

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• SciCrunch
• 13 years ago - by Anonymous

Software tool as parallel and distributed error correction algorithm for high-throughput short reads using CUDA and MPI parallel programming models.

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• SciCrunch
• 13 years ago - by Anonymous