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Genotyping-by-sequencing and SNP-arrays are complementary for detecting quantitative trait loci by tagging different haplotypes in association studies

Abstract Background Single Nucleotide Polymorphism (SNP) array and re-sequencing technologies have different properties (e.g. calling rate, minor allele frequency profile) and drawbacks (e.g. ascertainment bias). This lead us to study their complementarity and the consequences of using them separate...

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Autori principali: Sandra S. Negro, Emilie J. Millet, Delphine Madur, Cyril Bauland, Valérie Combes, Claude Welcker, François Tardieu, Alain Charcosset, Stéphane D. Nicolas
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMC 2019-07-01
Serie:BMC Plant Biology
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Accesso online:http://link.springer.com/article/10.1186/s12870-019-1926-4
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