Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

BACKGROUND: Targeted deep sequencing is a highly effective technology to identify known and novel single nucleotide variants (SNVs) with many applications in translational medicine, disease monitoring and cancer profiling. However, identification of SNVs using deep sequencing data is a challenging c...

全面介紹

Na minha lista:
書目詳細資料
發表在:BMC Med Genomics
Main Authors: Kleftogiannis, Dimitrios, Punta, Marco, Jayaram, Anuradha, Sandhu, Shahneen, Wong, Stephen Q., Gasi Tandefelt, Delila, Conteduca, Vincenza, Wetterskog, Daniel, Attard, Gerhardt, Lise, Stefano
格式: Artigo
語言:Inglês
出版: BioMed Central 2019
主題:
Technical Advance
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6679440/
https://ncbi.nlm.nih.gov/pubmed/31375105
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0557-9
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍