A pipeline for high throughput detection and mapping of SNPs from EST databases

Single nucleotide polymorphisms (SNPs) represent the most abundant type of genetic variation that can be used as molecular markers. The SNPs that are hidden in sequence databases can be unlocked using bioinformatic tools. For efficient application of these SNPs, the sequence set should be error-free...

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Detalles Bibliográficos
Autores principales: Anithakumari, A. M., Tang, Jifeng, van Eck, Herman J., Visser, Richard G. F., Leunissen, Jack A. M., Vosman, Ben, van der Linden, C. Gerard
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869401/
https://www.ncbi.nlm.nih.gov/pubmed/20502512
http://dx.doi.org/10.1007/s11032-009-9377-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869401/
https://www.ncbi.nlm.nih.gov/pubmed/20502512
http://dx.doi.org/10.1007/s11032-009-9377-5

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