Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation

Motivation: Genomic copy number variation (CNV) can influence susceptibility to common diseases. High-throughput measurement of gene copy number on large numbers of samples is a challenging, yet critical, stage in confirming observations from sequencing or array Comparative Genome Hybridization (CGH...

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Detalles Bibliográficos
Autores principales: Veal, Colin D., Xu, Hang, Reekie, Katherine, Free, Robert, Hardwick, Robert J., McVey, David, Brookes, Anthony J., Hollox, Edward J., Talbot, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722521/
https://www.ncbi.nlm.nih.gov/pubmed/23742985
http://dx.doi.org/10.1093/bioinformatics/btt330

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722521/
https://www.ncbi.nlm.nih.gov/pubmed/23742985
http://dx.doi.org/10.1093/bioinformatics/btt330

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