Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity

Copy-number variations (CNVs) are widespread in the human genome, but comprehensive assignments of integer locus copy-numbers (i.e., copy-number genotypes) that, for example, enable discrimination of homozygous from heterozygous CNVs, have remained challenging. Here we present CopySeq, a novel compu...

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Detalles Bibliográficos
Autores principales: Waszak, Sebastian M., Hasin, Yehudit, Zichner, Thomas, Olender, Tsviya, Keydar, Ifat, Khen, Miriam, Stütz, Adrian M., Schlattl, Andreas, Lancet, Doron, Korbel, Jan O.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978733/
https://www.ncbi.nlm.nih.gov/pubmed/21085617
http://dx.doi.org/10.1371/journal.pcbi.1000988

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978733/
https://www.ncbi.nlm.nih.gov/pubmed/21085617
http://dx.doi.org/10.1371/journal.pcbi.1000988

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