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Visualization tools for human structural variations identified by whole-genome sequencing
Visualizing structural variations (SVs) is a critical step for finding associations between SVs and human traits or diseases. Given that there are many sequencing platforms used for SV identification and given that how best to visualize SVs together with other data, such as read alignments and annot...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Singapore
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075883/ https://www.ncbi.nlm.nih.gov/pubmed/31666648 http://dx.doi.org/10.1038/s10038-019-0687-0 |