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VarSCAT: A computational tool for sequence context annotations of genomic variants
The sequence contexts of genomic variants play important roles in understanding biological significances of variants and potential sequencing related variant calling issues. However, methods for assessing the diverse sequence contexts of genomic variants such as tandem repeats and unambiguous annota...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10446208/ https://www.ncbi.nlm.nih.gov/pubmed/37566612 http://dx.doi.org/10.1371/journal.pcbi.1010727 |