SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes

Copy number variants are duplications and deletions of the genome that play an important role in phenotypic changes and human disease. Many software applications have been developed to detect copy number variants using either whole-genome sequencing or whole-exome sequencing data. However, there is...

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Detalles Bibliográficos
Autores principales: Xing, Yue, Dabney, Alan R., Li, Xiao, Wang, Guosong, Gill, Clare A., Casola, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046838/
https://www.ncbi.nlm.nih.gov/pubmed/32153642
http://dx.doi.org/10.3389/fgene.2020.00082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046838/
https://www.ncbi.nlm.nih.gov/pubmed/32153642
http://dx.doi.org/10.3389/fgene.2020.00082

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