Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
about
Implications of genetic heterogeneity in cancerNext-generation sequencing in clinical virology: Discovery of new virusesInfluenza treatment and prophylaxis with neuraminidase inhibitors: a reviewReverse Chemical Genetics: Comprehensive Fitness Profiling Reveals the Spectrum of Drug Target InteractionsSensitive Detection and Simultaneous Discrimination of Influenza A and B Viruses in Nasopharyngeal Swabs in a Single Assay Using Next-Generation Sequencing-Based DiagnosticsChallenges and opportunities in estimating viral genetic diversity from next-generation sequencing dataError baseline rates of five sample preparation methods used to characterize RNA virus populationsUsing high-throughput sequencing to leverage surveillance of genetic diversity and oseltamivir resistance: a pilot study during the 2009 influenza A(H1N1) pandemic.A Systematic Assessment of Accuracy in Detecting Somatic Mosaic Variants by Deep Amplicon Sequencing: Application to NF2 Gene.Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation.Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callersVarBin, a novel method for classifying true and false positive variants in NGS data.Ultra-deep pyrosequencing (UDPS) data treatment to study amplicon HCV minor variants.Detection of somatic mutations in tumors using unaligned clonal sequencing data.Distinguishing low frequency mutations from RT-PCR and sequence errors in viral deep sequencing data.ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clusteringRVD2: an ultra-sensitive variant detection model for low-depth heterogeneous next-generation sequencing data.Development and validation of a clinical trial patient stratification assay that interrogates 27 mutation sites in MAPK pathway genes.Variational inference for rare variant detection in deep, heterogeneous next-generation sequencing dataA programmable method for massively parallel targeted sequencing.Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq.Detection of Emerging Vaccine-Related Polioviruses by Deep Sequencing.Targeted sequencing library preparation by genomic DNA circularization.A new approach for detecting low-level mutations in next-generation sequence data.Detection of ultra-rare mutations by next-generation sequencing.Read length versus depth of coverage for viral quasispecies reconstructionUltra-deep mutant spectrum profiling: improving sequencing accuracy using overlapping read pairsRVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing.Single-tube, highly parallel mutation enrichment in cancer gene panels by use of temperature-tolerant COLD-PCR.Accurate single nucleotide variant detection in viral populations by combining probabilistic clustering with a statistical test of strand biasPerformance of common analysis methods for detecting low-frequency single nucleotide variants in targeted next-generation sequence dataMassively parallel sequencing fails to detect minor resistant subclones in tissue samples prior to tyrosine kinase inhibitor therapy.Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis.Limited Variation in BK Virus T-Cell Epitopes Revealed by Next-Generation Sequencing.DNA Barcoding through Quaternary LDPC Codes.QQ-SNV: single nucleotide variant detection at low frequency by comparing the quality quantiles.Third-generation sequencing techniques and applications to drug discovery.Detection of base substitution-type somatic mosaicism of the NLRP3 gene with >99.9% statistical confidence by massively parallel sequencing.Ultra-precise detection of mutations by droplet-based amplification of circularized DNA.Measurements of Intrahost Viral Diversity Are Extremely Sensitive to Systematic Errors in Variant Calling.
P2860
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P2860
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@ast
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@en
type
label
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@ast
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@en
prefLabel
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@ast
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@en
P2093
P2860
P356
P1476
Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
@en
P2093
Georges Natsoulis
Hanlee P Ji
Jason Buenrostro
Mark Winters
Nancy Zhang
Omkar Muralidharan
Patrick Flaherty
Sheldon Brown
P2860
P356
10.1093/NAR/GKR861
P407
P577
2011-10-19T00:00:00Z