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Proper Citation: m6ASNP: Annotation of genetic variants by m6A function (RRID:SCR_016048)
Description: Web server implemented in JAVA and PHP for annotating genetic variants by m6A function. It predicts and annotates N6-methyladenosine (m6A) alterations from genetic variants data such as germline SNPs or cancer somatic mutations. It employs two accurate prediction models for human and mouse using Random Forest algorithm. It conducts a statistical analysis for all the predicted m6A alterations. Provides statistical diagrams and a genome browser to visualize the topology characteristics of predicted m6A alterations.
Synonyms: m6ASNP
Resource Type: data access protocol, data analysis software, data processing software, data visualization software, software application, software resource, web service
Defining Citation: PMID:29617790, DOI:10.1093/gigascience/giy035
Keywords: N6-methyladenosine (m6A), variant annotation, effect prediction, random forest, miclip, m6a, mutant
Funding: China Postdoctoral Science Foundation 2017M622864; Fundamental Research Funds for the Central Universities No. 17lgpy106; Guangdong Natural Science Foundation 2014TQ01R387; National Key Research and Development Program 2017YFA0106700; National Natural Science Foundation of China 31771462
Availability: Free, Available for download, Freely available
Resource Name: m6ASNP: Annotation of genetic variants by m6A function
Resource ID: SCR_016048
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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
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