2016
DOI: 10.1371/journal.pone.0152632
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Correction: Design and Characterization of a 52K SNP Chip for Goats

Abstract: We have forgotten to thank our collaborators who provided the Creole samples. The Acknowledgements section should read:

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Cited by 13 publications
(7 citation statements)
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“…This indicated that Chinese goat breeds had lower genetic variation than global goat breeds. However, we cannot rule out ascertainment bias caused by sample size and the Illumina GoatSNP50 BeadChip ( Tosser-Klopp et al, 2016 ) designed using a non-Chinese goat background. The SNP panel used in this study was developed based on the sequence data of diverse goat breeds, including Alpine, Boer, Creole, Katjang, Saanen, and Savanna goats ( Tosser-Klopp et al, 2016 ), which reduced the SNP ascertainment bias to a certain extent.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…This indicated that Chinese goat breeds had lower genetic variation than global goat breeds. However, we cannot rule out ascertainment bias caused by sample size and the Illumina GoatSNP50 BeadChip ( Tosser-Klopp et al, 2016 ) designed using a non-Chinese goat background. The SNP panel used in this study was developed based on the sequence data of diverse goat breeds, including Alpine, Boer, Creole, Katjang, Saanen, and Savanna goats ( Tosser-Klopp et al, 2016 ), which reduced the SNP ascertainment bias to a certain extent.…”
Section: Discussionmentioning
confidence: 99%
“…However, we cannot rule out ascertainment bias caused by sample size and the Illumina GoatSNP50 BeadChip ( Tosser-Klopp et al, 2016 ) designed using a non-Chinese goat background. The SNP panel used in this study was developed based on the sequence data of diverse goat breeds, including Alpine, Boer, Creole, Katjang, Saanen, and Savanna goats ( Tosser-Klopp et al, 2016 ), which reduced the SNP ascertainment bias to a certain extent. Focusing on Jiangxi goat breeds, the current Guangfeng population had lower values of F ROH and F HOM than the Ganxi population and previous Guangfeng population.…”
Section: Discussionmentioning
confidence: 99%
“…The PCR amplification steps, PCR reaction concentrations, and PCR programs, including the sequencing technology, were carried out as described in Tarekegn et al [20]. For analysis of autosomal marker-based variation, 324 animals representing all four populations of Cameroon indigenous goats (Central Highland: n = 94; North-west Highland: n = 166; Forest goat: n = 31, and Djallonke: n = 33) were genotyped using the Caprine 50K SNP chip panel [34]. For comparison, we included genotype data from six Ethiopian indigenous goat populations (Ambo: n = 119; Afar: n = 49; Keffa: n = 51; Gumez: n = 42; Long-eared Somali: n = 48; Nubian: n = 47), representing East Africa; Egyptian Barki goat (n = 52) and Moroccan goat (n = 30), representing north Africa; one population from Iran (n = 9), and Cashmere goat (n = 108) from China.…”
Section: Methodsmentioning
confidence: 99%
“…All the four Cameroon goat populations analyzed and the 10 reference populations were genotyped using the caprine 50K SNP BeadChip array (Illumina Inc., San Diego, CA) [34]. Autosomal SNPs were filtered for call rate by sample and marker ≥ 90% and minor allele frequency (MAF) ≥ 5%.…”
Section: Methodsmentioning
confidence: 99%
“…In dairy cattle and sheep, this method has proved more efficient than direct imputation from lowest density to sequence [2,3]. In goats, the only genotyping tool available is a 50 k-chip (Illumina GoatSNP50 BeadChip) [4]. This means that imputation must be carried out directly from 50 k to sequence level.…”
Section: Introductionmentioning
confidence: 99%