Aquila_stLFR: diploid genome assembly based structural variant calling package for stLFR linked-reads

MOTIVATION: Identifying structural variants (SVs) is critical in health and disease, however, detecting them remains a challenge. Several linked-read sequencing technologies, including 10X Genomics, TELL-Seq and single tube long fragment read (stLFR), have been recently developed as cost-effective a...

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Detalles Bibliográficos
Autores principales: Liu, Yichen Henry, Grubbs, Griffin L, Zhang, Lu, Fang, Xiaodong, Dill, David L, Sidow, Arend, Zhou, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Applications Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710574/
https://www.ncbi.nlm.nih.gov/pubmed/36700103
http://dx.doi.org/10.1093/bioadv/vbab007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710574/
https://www.ncbi.nlm.nih.gov/pubmed/36700103
http://dx.doi.org/10.1093/bioadv/vbab007

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