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Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data
Insertion and deletion (INDEL) mutations, the most common type of structural variance, are associated with several human diseases. The detection of INDELs through next-generation sequencing (NGS) is becoming more common due to the decrease in costs, the increase in efficiency, and sensitivity improv...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549930/ https://www.ncbi.nlm.nih.gov/pubmed/28792971 http://dx.doi.org/10.1371/journal.pone.0182272 |