A genome-wide approach for detecting novel insertion-deletion variants of mid-range size

We present SWAN, a statistical framework for robust detection of genomic structural variants in next-generation sequencing data and an analysis of mid-range size insertion and deletions (<10 Kb) for whole genome analysis and DNA mixtures. To identify these mid-range size events, SWAN collectively...

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Detalles Bibliográficos
Autores principales: Xia, Li C., Sakshuwong, Sukolsak, Hopmans, Erik S., Bell, John M., Grimes, Susan M., Siegmund, David O., Ji, Hanlee P., Zhang, Nancy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009736/
https://www.ncbi.nlm.nih.gov/pubmed/27325742
http://dx.doi.org/10.1093/nar/gkw481

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009736/
https://www.ncbi.nlm.nih.gov/pubmed/27325742
http://dx.doi.org/10.1093/nar/gkw481

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