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Assessing myBaits Target Capture Sequencing Methodology Using Short-Read Sequencing for Variant Detection in Oat Genomics and Breeding.
Mahmood, Khalid; Sarup, Pernille; Oertelt, Lukas; Jahoor, Ahmed; Orabi, Jihad.
Afiliación
  • Mahmood K; Nordic Seed, Grindsnabevej 25, 8300 Odder, Denmark.
  • Sarup P; Nordic Seed, Grindsnabevej 25, 8300 Odder, Denmark.
  • Oertelt L; Nordic Seed Germany, Kirchhorster Str. 16, 31688 Nienstädt, Germany.
  • Jahoor A; Nordic Seed, Grindsnabevej 25, 8300 Odder, Denmark.
  • Orabi J; Nordic Seed Germany, Kirchhorster Str. 16, 31688 Nienstädt, Germany.
Genes (Basel) ; 15(6)2024 May 27.
Article en En | MEDLINE | ID: mdl-38927635
ABSTRACT
The integration of target capture systems with next-generation sequencing has emerged as an efficient tool for exploring specific genetic regions with a high resolution and facilitating the rapid discovery of novel alleles. Despite these advancements, the application of targeted sequencing methodologies, such as the myBaits technology, in polyploid oat species remains relatively unexplored. In this study, we utilized the myBaits target capture method offered by Daicel Arbor Biosciences to detect variants and assess their reliability for variant detection in oat genomics and breeding. Ten oat genotypes were carefully chosen for targeted sequencing, focusing on specific regions on chromosome 2A to detect variants. The selected region harbors 98 genes. Precisely designed baits targeting the genes within these regions were employed for the target capture sequencing. We employed various mappers and variant callers to identify variants. After the identification of variants, we focused on the variants identified via all variants callers to assess the applicability of the myBaits sequencing methodology in oat breeding. In our efforts to validate the identified variants, we focused on two SNPs, one deletion and one insertion identified via all variant callers in the genotypes KF-318 and NOS 819111-70 but absent in the remaining eight genotypes. The Sanger sequencing of targeted SNPs failed to reproduce target capture data obtained through the myBaits technology. Similarly, the validation of deletion and insertion variants via high-resolution melting (HRM) curve analysis also failed to reproduce target capture data, again suggesting limitations in the reliability of the myBaits target capture sequencing using short-read sequencing for variant detection in the oat genome. This study shed light on the importance of exercising caution when employing the myBaits target capture strategy for variant detection in oats. This study provides valuable insights for breeders seeking to advance oat breeding efforts and marker development using myBaits target capture sequencing, emphasizing the significance of methodological sequencing considerations in oat genomics research.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Avena / Polimorfismo de Nucleótido Simple / Secuenciación de Nucleótidos de Alto Rendimiento / Fitomejoramiento Idioma: En Revista: Genes (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Avena / Polimorfismo de Nucleótido Simple / Secuenciación de Nucleótidos de Alto Rendimiento / Fitomejoramiento Idioma: En Revista: Genes (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca
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