A collection of read depth profiles at structural variant breakpoints

SWaveform, a newly created open genome-wide resource for read depth signal in the vicinity of structural variant (SV) breakpoints, aims to boost development of computational tools and algorithms for discovery of genomic rearrangement events from sequencing data. SVs are a dominant force shaping geno...

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Detalles Bibliográficos
Autores principales: Bezdvornykh, Igor, Cherkasov, Nikolay, Kanapin, Alexander, Samsonova, Anastasia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079824/
https://www.ncbi.nlm.nih.gov/pubmed/37024526
http://dx.doi.org/10.1038/s41597-023-02076-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079824/
https://www.ncbi.nlm.nih.gov/pubmed/37024526
http://dx.doi.org/10.1038/s41597-023-02076-4

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