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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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On page 69 showing 1361 ~ 1380 out of 2,818 results
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  • RRID:SCR_011923

    This resource has 10+ mentions.

http://phylopythias.bifo.helmholtz-hzi.de/index.php?phase=wait

Web Server for Taxonomic Assignment of Metagenome Sequences that is a fast and accurate sequence composition-based classifier that utilizes the hierarchical relationships between clades. Taxonomic assignments with the web server can be made with a generic model, or with sample-specific models that users can specify and create. Several interactive visualization modes and multiple download formats allow quick and convenient analysis and downstream processing of taxonomic assignments.

Proper citation: PhyloPythiaS (RRID:SCR_011923) Copy   


http://www.hsls.pitt.edu/

Database access to information services, educational opportunities, and resources in print and electronic format to faculty, students, and researchers in the schools of the health sciences.

Proper citation: University of Pittsburgh, Health Sciences Library System (RRID:SCR_011975) Copy   


  • RRID:SCR_011978

    This resource has 10+ mentions.

http://omabrowser.org/cgi-bin/gateway.pl

A database that identifies orthologs among publicly available, complete genomes. It offers a comprehensive search and numerous display options for 4.7 million proteins from 1000 species. The main features are the orthologous relationships which can be accessed either group-wise, where all group members are orthologous to all other group members, or on a sequence-centric basis, where for a given protein all its orthologs in all other species are displayed.

Proper citation: OMA Browser (RRID:SCR_011978) Copy   


  • RRID:SCR_010923

    This resource has 10+ mentions.

http://compbio.med.harvard.edu/CGHweb/

Data analysis service enabling users to analyse their array-CGH data with multiple algorithms simultaneously.

Proper citation: CGHweb (RRID:SCR_010923) Copy   


  • RRID:SCR_012035

http://gsgator.ewha.ac.kr/

A web-based platform for functional interpretation of gene sets with features such as cross-species Gene Set Analysis (GSA), Flexible and Interactive GSA, simultaneous GSA for multiple gene set, and and a fully integrated network viewer for both visualizing GSA results and molecular networks.

Proper citation: gsGator (RRID:SCR_012035) Copy   


  • RRID:SCR_011980

    This resource has 500+ mentions.

https://www.orthodb.org/

Database of orthologous protein coding genes across vertebrates, arthropods, fungi, basal metazoans, and bacteria.

Proper citation: OrthoDB (RRID:SCR_011980) Copy   


  • RRID:SCR_011985

http://core-genomics.blogspot.de/

This blog focusses on next-generation sequencing and microarray technologies.

Proper citation: CoreGenomics (RRID:SCR_011985) Copy   


  • RRID:SCR_010897

http://cosmoss.org/bm/plantapdb

A phylogeny-based comprehensive database of plant transcription associated proteins.

Proper citation: PlanTAPDB (RRID:SCR_010897) Copy   


  • RRID:SCR_011986

    This resource has 1+ mentions.

http://www.bio-itworld.com/

A leading source of news on technology and innovation in life sciences IT, informatics, genomics, next-gen, drug discovery, development, and clinical trials.

Proper citation: Bio-IT World (RRID:SCR_011986) Copy   


  • RRID:SCR_010909

    This resource has 10+ mentions.

http://hyperbrowser.uio.no/hb/

A generic web-based system, providing statistical methodology and computing power to handle a variety of biological inquires on genomic datasets.

Proper citation: Genomic HyperBrowser (RRID:SCR_010909) Copy   


  • RRID:SCR_011796

    This resource has 500+ mentions.

https://genome-cancer.ucsc.edu/

A suite of web-based tools to visualize, integrate and analyze cancer genomics and its associated clinical data. It is possible to display your own clinical data within one of their datasets.

Proper citation: UCSC Cancer Genomics Browser (RRID:SCR_011796) Copy   


  • RRID:SCR_011951

    This resource has 100+ mentions.

http://weizhong-lab.ucsd.edu/metagenomic-analysis/

A customizable web server for fast metagenomic analysis.

Proper citation: WebMGA (RRID:SCR_011951) Copy   


  • RRID:SCR_012007

http://www.genoread.org/

A sequence verification pipeline where users can submit trace files to verify if a clone''s physical sequence matches its reference sequence.

Proper citation: GenoREAD (RRID:SCR_012007) Copy   


http://www.cancerrxgene.org/

A genomics database project is an academic research program to identify molecular features of cancers that predict response to anti-cancer drugs.

Proper citation: Genomics of Drug Sensitivity in Cancer (RRID:SCR_011956) Copy   


http://cdwscience.blogspot.fr/

A blog about genetics, genomics, and medical research.

Proper citation: My Biomedical Informatics Blog (RRID:SCR_012011) Copy   


  • RRID:SCR_012013

    This resource has 1+ mentions.

http://cbbiweb.uthscsa.edu/KMethylomes/

Datbase and web-based system for visualization and analysis of genome-wide methylation data of human cancers.

Proper citation: Cancer Methylome System (RRID:SCR_012013) Copy   


http://54.235.254.95/histonehits/

A database for histone mutations and their phenotypes.

Proper citation: Histone Systematic Mutation Database (RRID:SCR_012015) Copy   


  • RRID:SCR_012014

    This resource has 10+ mentions.

http://dbcat.cgm.ntu.edu.tw/

A database of CpG islands and analytical tools for identifying comprehensive methylation profiles in cancer cells.

Proper citation: DBCAT (RRID:SCR_012014) Copy   


  • RRID:SCR_012776

    This resource has 10+ mentions.

http://www.cravat.us/

A web-based application designed with an easy-to-use interface to facilitate the high-throughput assessment and prioritization of genes and missense alterations important for cancer tumorigenesis.

Proper citation: CRAVAT (RRID:SCR_012776) Copy   


  • RRID:SCR_012019

    This resource has 50+ mentions.

http://appris.bioinfo.cnio.es/

A database that houses annotations of human splice isoforms. It adds reliable protein structural and functional data and information from cross-species conservation. A visual representation of the annotations for each gene allows users to easily identify functional changes brought about by splicing events. In addition to collecting, integrating and analyzing reliable predictions of the effect of splicing events, it also selects a single reference sequence for each gene, termed the principal isoform, based on the annotations of structure, function and conservation for each transcript.

Proper citation: APPRIS (RRID:SCR_012019) Copy   



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