Simultaneous and complete genome sequencing of influenza A and B with high coverage by Illumina MiSeq Platform
Open Access
- 30 November 2013
- journal article
- research article
- Published by Elsevier BV in Journal of Virological Methods
- Vol. 193 (2), 394-404
- https://doi.org/10.1016/j.jviromet.2013.07.001
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and explorationBriefings in Bioinformatics, 2012
- Highly Sensitive and Specific Detection of Rare Variants in Mixed Viral Populations from Massively Parallel Sequence DataPLoS Computational Biology, 2012
- Virus Identification in Unknown Tropical Febrile Illness Cases Using Deep SequencingPLoS Neglected Tropical Diseases, 2012
- A framework for variation discovery and genotyping using next-generation DNA sequencing dataNature Genetics, 2011
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataGenome Research, 2010
- Fast and accurate long-read alignment with Burrows–Wheeler transformBioinformatics, 2010
- From where did the 2009 'swine-origin' influenza A virus (H1N1) emerge?Virology Journal, 2009
- Mixed Infection and the Genesis of Influenza Virus DiversityJournal of Virology, 2009
- Fast and accurate short read alignment with Burrows–Wheeler transformBioinformatics, 2009
- Phylogenetic analysis of the non-structural (NS) gene of influenza A viruses isolated from mallards in Northern Europe in 2005Virology Journal, 2008