a viral discovery methodology for clinical biopsy samples utilising massively parallel next generation sequencing一个病毒的发现方法为临床活检样本利用大规模并行下一代测序.pdfVIP
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a viral discovery methodology for clinical biopsy samples utilising massively parallel next generation sequencing一个病毒的发现方法为临床活检样本利用大规模并行下一代测序
A Viral Discovery Methodology for Clinical Biopsy
Samples Utilising Massively Parallel Next Generation
Sequencing
1 1 1 1 1 2
Gordon M. Daly , Nick Bexfield , Judith Heaney , Sam Stubbs , Antonia P. Mayer , Anne Palser , Paul
2 3 3 1 4 5
Kellam , Nizar Drou , Mario Caccamo , Laurence Tiley , Graeme J. M. Alexander , William Bernal ,
Jonathan L. Heeney1*
1 Department of Veterinary Medicine, The University of Cambridge, Cambridge, United Kingdom, 2 Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus,
Hinxton, Cambridge, United Kingdom, 3 The Genome Analysis Centre, Norwich Research Park, Norwich, United Kingdom, 4 Department of Hepatology, Addenbrookes
Hospital, Cambridge University Hospitals National Health Services Foundation Trust, Cambridge, United Kingdom, 5 Institute of Liver Studies, King’s College London
School of Medicine, King’s College Hospital, Denmark Hill, London, United Kingdom
Abstract
Here we describe a virus discovery protocol for a range of different virus genera, that can be applied to biopsy-sized tissue
samples. Our viral enrichment procedure, validated using canine and human liver samples, significantly improves viral read
copy number and increases the length of viral contigs that can be generated by de novo assembly. This in turn enables the
Illumina next generation sequencing (NGS) platform to be used as an effective tool for viral discovery from tissue samples.
Citation: Daly GM, Bexfield N, Heaney J, Stubbs S, Mayer AP, et al. (2011) A Viral Discovery Methodology for Clinical Biopsy Samples Utilising Massively Parallel
Next Generation Sequencing. PLoS ONE 6(12): e28879. doi:10.1371/
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