{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,13]],"date-time":"2024-05-13T17:54:45Z","timestamp":1715622885913},"reference-count":21,"publisher":"Pivot Science Publications Corporation","license":[{"start":{"date-parts":[[2023,6,10]],"date-time":"2023-06-10T00:00:00Z","timestamp":1686355200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Hum Popul Genet Genom"],"DOI":"10.47248\/hpgg2303020004","type":"journal-article","created":{"date-parts":[[2023,6,10]],"date-time":"2023-06-10T04:27:44Z","timestamp":1686371264000},"page":"1-12","source":"Crossref","is-referenced-by-count":2,"title":["Mutation Rate (Under)estimation through Mendelian Incompatibilities"],"prefix":"10.47248","author":[{"given":"Antonio","family":"Amorim","sequence":"first","affiliation":[{"name":"IPATIMUP, Rua J\u00falio Amaral de Carvalho, 45, 4200-135 Porto, Portugal"}]}],"member":"26871","published-online":{"date-parts":[[2023,6,10]]},"reference":[{"key":"ref0","doi-asserted-by":"publisher","unstructured":"Nachman MW, Crowell SL. Estimate of the mutation rate per nucleotide in humans. Genetics. 2000;156(1):297\u2013304.","DOI":"10.1093\/genetics\/156.1.297"},{"key":"ref1","doi-asserted-by":"publisher","unstructured":"Tian X, Cai R, Browning SR. Estimating the genome-wide mutation rate from thousands of unrelated individuals. Am J Hum Genet. 2022;109(12):2178\u20132184.","DOI":"10.1101\/2022.07.11.499645"},{"key":"ref2","doi-asserted-by":"publisher","unstructured":"J\u00f3nsson H, Sulem P, Arnadottir GA, P\u00e1lsson G, Eggertsson HP, Kristmundsdottir S, et al. Multiple transmissions of de novo mutations in families. Nat Genet. 2018;50(12):1674\u20131680.","DOI":"10.1038\/s41588-018-0259-9"},{"key":"ref3","doi-asserted-by":"publisher","unstructured":"Chakraborty R, Stivers DN, Zhong Y. Estimation of mutation rates from parentage exclusion data: applications to STR and VNTR loci. Mutat Res. 1996;354(1):41\u201348.","DOI":"10.1016\/0027-5107(96)00014-0"},{"key":"ref4","doi-asserted-by":"publisher","unstructured":"Dawid AP, Mortera J, Pascali VL. Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing. Forensic Sci Int. 2001;124(1):55\u201361.","DOI":"10.1016\/s0379-0738(01)00564-3"},{"key":"ref5","doi-asserted-by":"publisher","unstructured":"Brenner CH. Multiple mutations, covert mutations and false exclusions in paternity casework. Int Congr Ser. 2004;1261:112\u2013114.","DOI":"10.1016\/s0531-5131(03)01843-0"},{"key":"ref6","doi-asserted-by":"crossref","unstructured":"Vicard P, Dawid AP. A statistical treatment of biases affecting the estimation of mutation rates. Mutat Res. 2004;547(1-2):19\u201333.","DOI":"10.1016\/j.mrfmmm.2003.11.005"},{"key":"ref7","doi-asserted-by":"publisher","unstructured":"Vicard P, Dawid AP, Mortera J, Lauritzen SL. Estimating mutation rates from paternity casework. Forensic Sci Int Genet. 2008;2(1):9\u201318.","DOI":"10.1016\/j.fsigen.2007.07.002"},{"key":"ref8","doi-asserted-by":"crossref","unstructured":"Scally A. Mutation rates and the evolution of germline structure. Philos Trans R Soc Lond B Biol Sci. 2016;371(1699):20150137.","DOI":"10.1098\/rstb.2015.0137"},{"key":"ref9","doi-asserted-by":"publisher","unstructured":"Fu YX, Huai H. Estimating mutation rate: How to count mutations?. Genetics. 2003;164(2):797\u2013805.","DOI":"10.1093\/genetics\/164.2.797"},{"key":"ref10","doi-asserted-by":"publisher","unstructured":"Cano AV, Gitschlag BL, Rozho\u0148ov\u00e1 H, Stoltzfus A, McCandlish DM, Payne JL. Mutation bias and the predictability of evolution. Philos Trans R Soc Lond B Biol Sci. 2023;378(1877):20220055.","DOI":"10.32942\/x2qg67"},{"key":"ref11","doi-asserted-by":"publisher","unstructured":"Pinto N, Gusm\u00e3o L, Amorim A. Mutation and mutation rates at Y chromosome specific Short Tandem Repeat Polymorphisms (STRs): A reappraisal. Forensic Sci Int. Genet. 2014;9:20\u201324.","DOI":"10.1016\/j.fsigen.2013.10.008"},{"key":"ref12","doi-asserted-by":"publisher","unstructured":"Amorim A, Pinto N. Estimates of mutation rates from incompatibilities are misleading - guidelines for publication and retrieval of mutation data urgently needed. Forensic Sci Int Genet Suppl Ser. 2019;7(1):612\u2013613.","DOI":"10.1016\/j.fsigss.2019.10.110"},{"key":"ref13","doi-asserted-by":"publisher","unstructured":"Ant\u00e3o-Sousa S, Conde-Sousa E, Gusm\u00e3o L, Amorim A, Pinto N. Estimations of mutation rates depend on population allele frequency distribution: The case of autosomal microsatellites. Genes. 2022;13(7):1248.","DOI":"10.3390\/genes13071248"},{"key":"ref14","doi-asserted-by":"crossref","unstructured":"Jacquard A. The Genetic Structure of Populations. Berlin: Springer; 1974.","DOI":"10.1007\/978-3-642-88415-3"},{"key":"ref15","doi-asserted-by":"publisher","unstructured":"Slooten K, Ricciardi F. Estimation of mutation probabilities for autosomal STR markers. Forensic Sci Int Genet. 2013;7(3):337\u2013344.","DOI":"10.1016\/j.fsigen.2013.01.006"},{"key":"ref16","doi-asserted-by":"publisher","unstructured":"Scally A, Durbin R. Revising the human mutation rate: Implications for understanding human evolution. Nat Rev Genet. 2012;13(10):745\u2013753.","DOI":"10.1038\/nrg3295"},{"key":"ref17","doi-asserted-by":"publisher","unstructured":"S\u00e9gurel L, Wyman MJ, Przeworski M. Determinants of mutation rate variation in the human germline. Annu Rev Genomics Hum Genet. 2014;15:47\u201370.","DOI":"10.1146\/annurev-genom-031714-125740"},{"key":"ref18","doi-asserted-by":"publisher","unstructured":"Bergeron LA, Besenbacher S, Zheng J, Li P, Bertelsen MF, Quintard B, et al. Evolution of the germline mutation rate across vertebrates. Nature. 2023;615:285\u2013291.","DOI":"10.1038\/s41586-023-05752-y"},{"key":"ref19","doi-asserted-by":"publisher","unstructured":"Douglas JA, Skol AD, Boehnke M. Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. Am J Hum Genet. 2002;70(2):487\u2013495.","DOI":"10.1086\/338919"},{"key":"ref20","doi-asserted-by":"publisher","unstructured":"Gordon D, Heath SC, Ott J. True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms. Hum Hered. 1999;49(2):65\u201370.","DOI":"10.1159\/000022846"}],"container-title":["Human Population Genetics and Genomics"],"original-title":[],"language":"en","deposited":{"date-parts":[[2023,6,10]],"date-time":"2023-06-10T04:27:48Z","timestamp":1686371268000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.pivotscipub.com\/hpgg\/3\/2\/0004"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,6,10]]},"references-count":21,"URL":"https:\/\/doi.org\/10.47248\/hpgg2303020004","archive":["Portico"],"relation":{},"subject":[],"published":{"date-parts":[[2023,6,10]]}}}