GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing

The combined analysis of haplotype panels with phenotype clinical cohorts is a common approach to explore the genetic architecture of human diseases. However, genetic studies are mainly based on single nucleotide variants (SNVs) and small insertions and deletions (indels). Here, we contribute to fil...

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Detalles Bibliográficos
Autores principales: Valls-Margarit, Jordi, Galván-Femenía, Iván, Matías-Sánchez, Daniel, Blay, Natalia, Puiggròs, Montserrat, Carreras, Anna, Salvoro, Cecilia, Cortés, Beatriz, Amela, Ramon, Farre, Xavier, Lerga-Jaso, Jon, Puig, Marta, Sánchez-Herrero, Jose Francisco, Moreno, Victor, Perucho, Manuel, Sumoy, Lauro, Armengol, Lluís, Delaneau, Olivier, Cáceres, Mario, de Cid, Rafael, Torrents, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Computational Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934637/
https://www.ncbi.nlm.nih.gov/pubmed/35176773
http://dx.doi.org/10.1093/nar/gkac076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934637/
https://www.ncbi.nlm.nih.gov/pubmed/35176773
http://dx.doi.org/10.1093/nar/gkac076

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