Protocol for unbiased, consolidated variant calling from whole exome sequencing data

Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of genomes (exomes). However, WES analysis can be challenging because of the complexity of the data. Here, we describe a consolidated protocol for unbiased WES analysis. The protocol uses three variant call...

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Detalles Bibliográficos
Autores principales: Verrou, Kleio-Maria, Pavlopoulos, Georgios A., Moulos, Panagiotis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163752/
https://www.ncbi.nlm.nih.gov/pubmed/35669050
http://dx.doi.org/10.1016/j.xpro.2022.101418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163752/
https://www.ncbi.nlm.nih.gov/pubmed/35669050
http://dx.doi.org/10.1016/j.xpro.2022.101418

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