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Additional file 1: Table S1. of Highly accurate sequence imputation enables precise QTL mapping in Brown Swiss cattle

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Breed codes and number of individuals per breed within the fifth run of the 1000 Bull Genomes Project. Table S2. Average number of SNPs per minor allele frequency class in S5, S6 and S7. Table S3. Imputation accuracy per breed in S1. Table S4. Imputation accuracy per minor allele frequency class in S5, S6, S7. Table S5. p-values and SNPs with Bonferroni corrected significant association for FCearly. Chr is the chromosome and Pos is the position of the SNP, they correspond to UMD3.1. R2 is an imputation quality measure provided by Minimac and P is the p-value from the genome-wide association study. Table S6. p-values and SNPs with Bonferroni corrected significant association for FClate. Chr is the chromosome and Pos is the position of the SNP, they correspond to UMD3.1. R2 is an imputation quality measure provided by Minimac and P is the p-value from the genome-wide association study. (XLSX 169Â kb)
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