Accurate single nucleotide variant detection in viral populations by combining probabilistic clustering with a statistical test of strand bias
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Accurate single nucleotide variant detection in viral populations by combining probabilistic clustering with a statistical test of strand bias
Authors
Keywords
Viral Population, Probabilistic Cluster, Strand Bias, True Haplotype, Deep Sequencing Experiment
Journal
BMC GENOMICS
Volume 14, Issue 1, Pages 501
Publisher
Springer Nature
Online
2013-07-25
DOI
10.1186/1471-2164-14-501
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- GemSIM: general, error-model based simulator of next-generation sequencing data
- (2012) Kerensa E McElroy et al. BMC GENOMICS
- The effect of strand bias in Illumina short-read sequencing data
- (2012) Yan Guo et al. BMC GENOMICS
- LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets
- (2012) Andreas Wilm et al. NUCLEIC ACIDS RESEARCH
- Highly Sensitive and Specific Detection of Rare Variants in Mixed Viral Populations from Massively Parallel Sequence Data
- (2012) Alexander R. Macalalad et al. PLoS Computational Biology
- Whole Genome Deep Sequencing of HIV-1 Reveals the Impact of Early Minor Variants Upon Immune Recognition During Acute Infection
- (2012) Matthew R. Henn et al. PLoS Pathogens
- Landscape of Next-Generation Sequencing Technologies
- (2011) Thomas P. Niedringhaus et al. ANALYTICAL CHEMISTRY
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
- (2011) H. Li BIOINFORMATICS
- Accuracy and quality assessment of 454 GS-FLX Titanium pyrosequencing
- (2011) André Gilles et al. BMC GENOMICS
- Genotype and SNP calling from next-generation sequencing data
- (2011) Rasmus Nielsen et al. NATURE REVIEWS GENETICS
- Ultrasensitive detection of rare mutations using next-generation targeted resequencing
- (2011) Patrick Flaherty et al. NUCLEIC ACIDS RESEARCH
- Ultra-deep sequencing for the analysis of viral populations
- (2011) Niko Beerenwinkel et al. Current Opinion in Virology
- Sequential Bottlenecks Drive Viral Evolution in Early Acute Hepatitis C Virus Infection
- (2011) Rowena A. Bull et al. PLoS Pathogens
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- Genome variation discovery with high-throughput sequencing data
- (2010) A. V. Dalca et al. BRIEFINGS IN BIOINFORMATICS
- Deep Sequencing of a Genetically Heterogeneous Sample: Local Haplotype Reconstruction and Read Error Correction
- (2010) Osvaldo Zagordi et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- Error correction of next-generation sequencing data and reliable estimation of HIV quasispecies
- (2010) Osvaldo Zagordi et al. NUCLEIC ACIDS RESEARCH
- Dynamics of HIV-1 Quasispecies during Antiviral Treatment Dissected Using Ultra-Deep Pyrosequencing
- (2010) Charlotte Hedskog et al. PLoS One
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples
- (2009) Daniel C. Koboldt et al. BIOINFORMATICS
- Minority Quasispecies of Drug‐Resistant HIV‐1 That Lead to Early Therapy Failure in Treatment‐Naive and ‐Adherent Patients
- (2008) Karin J. Metzner et al. CLINICAL INFECTIOUS DISEASES
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started