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Detection of de novo copy number deletions from targeted sequencing of trios

MOTIVATION: De novo copy number deletions have been implicated in many diseases, but there is no formal method to date that identifies de novo deletions in parent-offspring trios from capture-based sequencing platforms. RESULTS: We developed Minimum Distance for Targeted Sequencing (MDTS) to fill th...

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Detalles Bibliográficos
Autores principales: Fu, Jack M, Leslie, Elizabeth J, Scott, Alan F, Murray, Jeffrey C, Marazita, Mary L, Beaty, Terri H, Scharpf, Robert B, Ruczinski, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378941/
https://www.ncbi.nlm.nih.gov/pubmed/30084993
http://dx.doi.org/10.1093/bioinformatics/bty677
Descripción
Sumario:MOTIVATION: De novo copy number deletions have been implicated in many diseases, but there is no formal method to date that identifies de novo deletions in parent-offspring trios from capture-based sequencing platforms. RESULTS: We developed Minimum Distance for Targeted Sequencing (MDTS) to fill this void. MDTS has similar sensitivity (recall), but a much lower false positive rate compared to less specific CNV callers, resulting in a much higher positive predictive value (precision). MDTS also exhibited much better scalability. AVAILABILITY AND IMPLEMENTATION: MDTS is freely available as open source software from the Bioconductor repository. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.