Targeted interrogation of copy number variation using SCIMMkit

Summary: Copy number variants (CNVs) contribute substantially to human genomic diversity, and development of accurate and efficient methods for CNV genotyping is a central problem in exploring human genotype–phenotype associations. SCIMMkit provides a robust, integrated implementation of three previ...

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Detalles Bibliográficos
Autores principales: Zerr, Troy, Cooper, Gregory M., Eichler, Evan E., Nickerson, Deborah A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Applications Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796813/
https://www.ncbi.nlm.nih.gov/pubmed/19846438
http://dx.doi.org/10.1093/bioinformatics/btp606

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796813/
https://www.ncbi.nlm.nih.gov/pubmed/19846438
http://dx.doi.org/10.1093/bioinformatics/btp606

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