AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis

With the dramatic increase of pangenomic analysis, Human geneticists have generated large amount of genomic data including millions of small variants (SNV/indel) but also thousands of structural variations (SV) mainly from next-generation sequencing and array-based techniques. While the identificati...

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Detalles Bibliográficos
Autores principales: Geoffroy, Véronique, Guignard, Thomas, Kress, Arnaud, Gaillard, Jean-Baptiste, Solli-Nowlan, Tor, Schalk, Audrey, Gatinois, Vincent, Dollfus, Hélène, Scheidecker, Sophie, Muller, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Web Server Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262758/
https://www.ncbi.nlm.nih.gov/pubmed/34023905
http://dx.doi.org/10.1093/nar/gkab402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262758/
https://www.ncbi.nlm.nih.gov/pubmed/34023905
http://dx.doi.org/10.1093/nar/gkab402

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