The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research

Copy number variations (CNVs) are major causative contributors both in the genesis of genetic diseases and human neoplasias. While “High-Throughput” sequencing technologies are increasingly becoming the primary choice for genomic screening analysis, their ability to efficiently detect CNVs is still...

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Detalles Bibliográficos
Autores principales: Salgado, David, Armean, Irina M., Baudis, Michael, Beltran, Sergi, Capella-Gutierrez, Salvador, Carvalho-Silva, Denise, Dominguez Del Angel, Victoria, Dopazo, Joaquin, Furlong, Laura I., Gao, Bo, Garcia, Leyla, Gerloff, Dietlind, Gut, Ivo, Gyenesei, Attila, Habermann, Nina, Hancock, John M., Hanauer, Marc, Hovig, Eivind, Johansson, Lennart F., Keane, Thomas, Korbel, Jan, Lauer, Katharina B., Laurie, Steve, Leskošek, Brane, Lloyd, David, Marques-Bonet, Tomas, Mei, Hailiang, Monostory, Katalin, Piñero, Janet, Poterlowicz, Krzysztof, Rath, Ana, Samarakoon, Pubudu, Sanz, Ferran, Saunders, Gary, Sie, Daoud, Swertz, Morris A., Tsukanov, Kirill, Valencia, Alfonso, Vidak, Marko, Yenyxe González, Cristina, Ylstra, Bauke, Béroud, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Opinion Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311797/
https://www.ncbi.nlm.nih.gov/pubmed/34367618
http://dx.doi.org/10.12688/f1000research.24887.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311797/
https://www.ncbi.nlm.nih.gov/pubmed/34367618
http://dx.doi.org/10.12688/f1000research.24887.1

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