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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Bibliografski detalji
Izdano u:F1000Res
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: F1000 Research Limited 2020
Teme:
Opinion Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8311797/
https://ncbi.nlm.nih.gov/pubmed/34367618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.24887.1
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