Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation

BACKGROUND: With the rapid development of long-read sequencing technologies, it is possible to reveal the full spectrum of genetic structural variation (SV). However, the expensive cost, finite read length and high sequencing error for long-read data greatly limit the widespread adoption of SV calli...

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Detalles Bibliográficos
Autores principales: Jiang, Tao, Liu, Shiqi, Cao, Shuqi, Liu, Yadong, Cui, Zhe, Wang, Yadong, Guo, Hongzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588741/
https://www.ncbi.nlm.nih.gov/pubmed/34772337
http://dx.doi.org/10.1186/s12859-021-04422-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8588741/
https://www.ncbi.nlm.nih.gov/pubmed/34772337
http://dx.doi.org/10.1186/s12859-021-04422-y

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