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The discrepancy among single nucleotide variants detected by DNA and RNA high throughput sequencing data
BACKGROUND: High throughput sequencing technology enables the both the human genome and transcriptome to be screened at the single nucleotide resolution. Tools have been developed to infer single nucleotide variants (SNVs) from both DNA and RNA sequencing data. To evaluate how much difference can be...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629567/ https://www.ncbi.nlm.nih.gov/pubmed/28984205 http://dx.doi.org/10.1186/s12864-017-4022-x |