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PanSVR: Pan-Genome Augmented Short Read Realignment for Sensitive Detection of Structural Variations
The comprehensive discovery of structure variations (SVs) is fundamental to many genomics studies and high-throughput sequencing has become a common approach to this task. However, due the limited length, it is still non-trivial to state-of-the-art tools to accurately align short reads and produce h...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417358/ https://www.ncbi.nlm.nih.gov/pubmed/34490049 http://dx.doi.org/10.3389/fgene.2021.731515 |