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URL: http://code.google.com/p/snpdat/
Proper Citation: SNPdat (RRID:SCR_005187)
Description: A simple and easy to use high through-put analysis tool which can provide comprehensive annotation of both novel and known single nucleotide polymorphisms (SNPs) for any organism with a draft sequence and annotation. SNPdat makes possible analyses involving non-model organisms that are not supported by the vast majority of SNP annotation tools currently available. It is especially intended for use by researchers with limited bioinformatic experience.
Abbreviations: SNPdat
Synonyms: SNP Data Analysis Tool, SNPdat - A Simple High Throughput Analysis Tool for Annotating SNPs
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: PMID:23390980
Keywords: high through-put, single nucleotide polymorphism, annotation, gtf, gff, fasta, sequence analysis, genome, command line
Availability: GNU General Public License, v2, Acknowledgement requested
Resource Name: SNPdat
Resource ID: SCR_005187
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
