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Detecting differential copy number variation between groups of samples
We present a method to detect copy number variants (CNVs) that are differentially present between two groups of sequenced samples. We use a finite-state transducer where the emitted read depth is conditioned on the mappability and GC-content of all reads that occur at a given base position. In this...
Autores principales: | Lowe, Craig B., Sanchez-Luege, Nicelio, Howes, Timothy R., Brady, Shannon D., Daugherty, Rhea R., Jones, Felicity C., Bell, Michael A., Kingsley, David M. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793789/ https://www.ncbi.nlm.nih.gov/pubmed/29229672 http://dx.doi.org/10.1101/gr.206938.116 |
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