ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation

Structural genomic variations play an important role in human disease and phenotypic diversity. With the rise of high-throughput sequencing tools, mate-pair/paired-end/single-read sequencing has become an important technique for the detection and exploration of structural variation. Several analysis...

Descripción completa

Detalles Bibliográficos
Autores principales: Sante, Tom, Vergult, Sarah, Volders, Pieter-Jan, Kloosterman, Wigard P., Trooskens, Geert, De Preter, Katleen, Dheedene, Annelies, Speleman, Frank, De Meyer, Tim, Menten, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264741/
https://www.ncbi.nlm.nih.gov/pubmed/25503062
http://dx.doi.org/10.1371/journal.pone.0113800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264741/
https://www.ncbi.nlm.nih.gov/pubmed/25503062
http://dx.doi.org/10.1371/journal.pone.0113800

Ejemplares similares