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...

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Detalles Bibliográficos
Autores principales: Guo, Yan, Zhao, Shilin, Sheng, Quanhu, Samuels, David C, Shyr, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
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

Internet

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

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