Evaluating nanopore sequencing data processing pipelines for structural variation identification

BACKGROUND: Structural variations (SVs) account for about 1% of the differences among human genomes and play a significant role in phenotypic variation and disease susceptibility. The emerging nanopore sequencing technology can generate long sequence reads and can potentially provide accurate SV ide...

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Detalles Bibliográficos
Autores principales: Zhou, Anbo, Lin, Timothy, Xing, Jinchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857234/
https://www.ncbi.nlm.nih.gov/pubmed/31727126
http://dx.doi.org/10.1186/s13059-019-1858-1

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