Corrigendum Corrigendum to ‘‘Updated Brazilian STR allele frequency data using over 100,000 individuals: An analysis of CSF1PO, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, FGA, Penta D, Penta E, TH01, TPOX and vWA loci’’ [Forensic Sci. Int.: Genet. 6 (4) (2012) 504–509] Vitor Rezende da Costa Aguiar a,1 , Eldama ´ ria de Vargas Wolfgramm a,1 , Frederico Scott Varella Malta b,2 , Adriana Gonc ¸alves Bosque b,2 , Amanda de Castro Mafia b,2 , Vanessa Cristina de Oliveira Almeida b,2 , Fabiola de Andrade Caxito b,2 , Victor Cavalcanti Pardini b,2 , Alessandro Clayton Souza Ferreira b , Iu ´ ri Drumond Louro a, * a Nu ´cleo de Gene ´tica Humana e Molecular, Departamento de Cieˆncias Biolo ´gicas, Centro de Cieˆncias Humanas e Naturais, Universidade Federal do Espı´rito Santo, Av. Marechal Campos 1468, Campus de Maruı´pe, CEP 29040-090 Vito ´ria, ES, Brazil b Laborato ´rio Hermes Pardini, Departamento de Gene ´tica Molecular, Avenida das Nac ¸o˜es,2448 Portaria A, 32200-000 Vespasiano, MG, Brazil The following errors were originally undetected by authors. STR alleles 14.5 and 16.5 shown in Table 1 are inconsistent with tetranucleotidic repeats. Although these values are not critical to the overall weight of the article, a prompt correction is recommended. In Table 2, an input format mistake for the analysis performed in the Arlequin Software generated overestimated Fst values between all populations reported in this table. The current input format should produce correct results. Owing to the corrections made in the tables, some text changes. PAGE 1. ABSTRACT The original text: The number of individuals genotyped for each locus was: CSF1PO (113,526); D3S1358 (135,133); D5S818 (135,181); D7S820 (137,136); D8S1179 (134,211); D13S317 (137,161); D16S539 (136,942); D18S51 (136,739); D21S11 (130,014); FGA (135,839); Penta D (110,333); Penta E (128,055); TH01 (112,695); TPOX (123,102); vWA (127,415). Should be corrected to: The number of individuals genotyped for each locus was: CSF1PO (113,526); D3S1358 (135,132); D5S818 (135,181); D7S820 (137,136); D8S1179 (134,211); D13S317 (137,161); D16S539 (136,942); D18S51 (136,737); D21S11 (130,014); FGA (135,839); Penta D (110,333); Penta E (128,055); TH01 (112,695); TPOX (123,102); vWA (127,415). 2. Sampling The original text: The number of individuals genotyped for each locus was: CSF1PO (113,526); D3S1358 (135,133); D5S818 (135,181); D7S820 (137,136); D8S1179 (134,211); D13S317 (137,161); D16S539 (136,942); D18S51 (136,739); D21S11 (130,014); FGA (135,839); Penta D (110,333); Penta E (128,055); TH01 (112,695); TPOX (123,102); vWA (127,415). Should be corrected to: The number of individuals genotyped for each locus was: CSF1PO (113,526); D3S1358 (135,132); D5S818 (135,181); D7S820 (137,136); D8S1179 (134,211); D13S317 (137,161); D16S539 (136,942); D18S51 (136,737); D21S11 (130,014); FGA (135,839); Penta D (110,333); Penta E (128,055); TH01 (112,695); TPOX (123,102); vWA (127,415). PAGE 2. 5. Results and Conclusion 2 o paragraph The original text: Because the Brazilian population is the result of centuries of multiethnic crossings among Ameridians, Africans and Europeans, we compared our results with some of those populations. Pairwise analysis (Fst) demonstrated that the Brazilian population was more closely related to the Europeans for markers D3S1358, D7S820, D16S539 and TH01 and more similar to Sub-Saharan Africans according to markers FGA, Penta D, Penta E, D18S51, D21S11 and vWA. Comparing our results with other Brazilian population [4] showed a high degree of concordance for markers D18S51, CSF1PO and D5S818. AMOVA analysis showed marker TPOX with the highest index of variation among individuals of different populations (24.35%), as opposed to marker Penta E that showed the lowest index (5.96%). The Forensic Science International: Genetics 7 (2013) 321–325 DOI of original article: http://dx.doi.org/10.1016/j.fsigen.2011.07.005 * Corresponding author. Tel.: +55 27 3335 7251; fax: +55 27 335 7250. E-mail address: iurilouro@yahoo.com (I.D. Louro). 1 First and second authors contributed equally to this manuscript. 2 Tel.: +55 31 3629 4852; fax: +55 31 3629 4872. Contents lists available at SciVerse ScienceDirect Forensic Science International: Genetics jou r nal h o mep ag e: w ww .elsevier .co m /loc ate/fs ig 1872-4973/$ – see front matter ß 2012 Elsevier Ireland Ltd. All rights reserved. http://dx.doi.org/10.1016/j.fsigen.2012.11.008