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AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis
With the dramatic increase of pangenomic analysis, Human geneticists have generated large amount of genomic data including millions of small variants (SNV/indel) but also thousands of structural variations (SV) mainly from next-generation sequencing and array-based techniques. While the identificati...
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| Publicado en: | Nucleic Acids Res |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8262758/ https://ncbi.nlm.nih.gov/pubmed/34023905 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkab402 |
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