SVM(2): an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing data

Several bioinformatics methods have been proposed for the detection and characterization of genomic structural variation (SV) from ultra high-throughput genome resequencing data. Recent surveys show that comprehensive detection of SV events of different types between an individual resequenced genome...

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Detalles Bibliográficos
Autores principales: Chiara, Matteo, Pesole, Graziano, Horner, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467043/
https://www.ncbi.nlm.nih.gov/pubmed/22735696
http://dx.doi.org/10.1093/nar/gks606

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467043/
https://www.ncbi.nlm.nih.gov/pubmed/22735696
http://dx.doi.org/10.1093/nar/gks606

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