Similarities and differences between variants called with human reference genome HG19 or HG38

BACKGROUND: Reference genome selection is a prerequisite for successful analysis of next generation sequencing (NGS) data. Current practice employs one of the two most recent human reference genome versions: HG19 or HG38. To date, the impact of genome version on SNV identification has not been rigor...

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Detalles Bibliográficos
Autores principales: Pan, Bohu, Kusko, Rebecca, Xiao, Wenming, Zheng, Yuanting, Liu, Zhichao, Xiao, Chunlin, Sakkiah, Sugunadevi, Guo, Wenjing, Gong, Ping, Zhang, Chaoyang, Ge, Weigong, Shi, Leming, Tong, Weida, Hong, Huixiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419332/
https://www.ncbi.nlm.nih.gov/pubmed/30871461
http://dx.doi.org/10.1186/s12859-019-2620-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419332/
https://www.ncbi.nlm.nih.gov/pubmed/30871461
http://dx.doi.org/10.1186/s12859-019-2620-0

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