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ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information
BACKGROUND: Structural variations (SVs) change the structure of the genome and are therefore the causes of various diseases. Next-generation sequencing allows us to obtain a multitude of sequence data, some of which can be used to infer the position of SVs. METHODS: We developed a new method and imp...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287472/ https://www.ncbi.nlm.nih.gov/pubmed/22373054 http://dx.doi.org/10.1186/1471-2105-12-S14-S7 |