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mirDNMR is a database for the collection of gene-centered background DNMRs obtained from different methods and population variation data. The database has the following functions: (i) browse and search the background DNMRs of each gene predicted by four different methods, including GC content (DNMR-GC), sequence context (DNMR-SC), multiple factors (DNMR-MF) and local DNA methylation level (DNMR-DM); (ii) search variant frequencies in publicly available databases, including ExAC, ESP6500, UK10K, 1000G and dbSNP and (iii) investigate the DNM burden to prioritize candidate genes based on the four background DNMRs using three statistical methods (TADA, Binomial and Poisson test). In conclusion, mirDNMR can be widely used to identify the genetic basis of sporadic genetic diseases.
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FAIRsharing.org: mirDNMR; mirDNMR; DOI: https://doi.org/10.25504/FAIRsharing.68f4xz;
Last edited: Jan. 8, 2019, 1:23 p.m.; Last accessed: Jul 16 2020 3:13 p.m.
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Record added: Nov. 3, 2016, 12:12 p.m.
Nov. 8, 2016, 9:01 p.m. by The FAIRsharing Team.
Edits to 'https://fairsharing.org/FAIRsharing.68f4xz' by 'The FAIRsharing Team' at 21:01, 08 Nov 2016 (approved):
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Before: a gene-centered database of background de novo mutation rates in human
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mirDNMR: a gene-centered database of background de novo mutation rates in human.
Jiang Y,Li Z,Liu Z,Chen D,Wu W,Du Y,Ji L,Jin ZB,Li W,Wu J
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Nucleic Acids Res 2016
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