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on page 1 showing 4 out of 280 results

Cite this (SplitSeek, RRID:SCR_001012)

URL: https://omictools.com/splitseek-tool

Resource Type: Resource, software resource, data processing software, data analysis software, sequence analysis software, software application

THIS RESOURCE IS NO LONGER SUPPORTED, documented September 20, 2016. A program for de novo prediction of splice junctions in RNA-seq data.


Cite this (Pathology Diagnostics, RRID:SCR_001033)

URL: http://www.pathologydiagnostics.com

Resource Type: Resource, service resource, core facility, access service resource

THIS RESOURCE IS NO LONGER IN SERVICE, documented September 15, 2016. Pathology Diagnostics Ltd is an independent GCLP accredited histopathology research organisation delivering tissue, laboratory, and diagnostics services to industry Research and Development scientists engaged in drug and biomarker development.


Cite this (Seoul Cord Blood Bank, RRID:SCR_010514)

URL: http://www.newlifestemcell.com/about/seoul_01.asp

Resource Type: Resource, biomaterial supply resource, material resource, tissue bank

THIS RESOURCE IS NO LONGER IN SERVICE, documented August 22, 2016. An umbilical cord blood bank located in Seoul, South Korea.


Cite this (Genetic Alterations in Cancer, RRID:SCR_010533)

URL: http://www.niehs.nih.gov/news/newsletter/2006/march/science-genetic.cfm

Resource Type: Resource, data or information resource, database

THIS RESOURCE IS NO LONGER IN SERVICE, documented August 22, 2016. The NIEHS Genetic Alterations in Cancer (GAC) knowledgebase is a comprehensive collection of data compiled from studies reported in the published literature on genetic alterations in tumors associated with exposure to specific chemical, physical, or biological agents that can be linked to genes implicated in the development of cancers. GAC provides access to data from peer reviewed journals for hundreds of studies of gene mutations, loss of heterozygosity, and/or chromosome changes in tumors from humans, mice, or rats. Results are summarized in tables and graphic profiles that show the incidence (percent) of tumors with alterations in each gene that has been studied. Detailed data tables display results for each subject studied in the cited reference and the reference ID is hyperlinked to its PubMed abstract for more information. A mutation spectrum for individual genes and links to gene information from The Cancer Genome Anatomy Project and the Rat Genome Database are also provided.


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