Ultra-deep mutant spectrum profiling: improving sequencing accuracy using overlapping read pairs
about
Best practices for evaluating single nucleotide variant calling methods for microbial genomicsDetection of Low-Level Mixed-Population Drug Resistance in Mycobacterium tuberculosis Using High Fidelity Amplicon SequencingHigh-specificity detection of rare alleles with Paired-End Low Error Sequencing (PELE-Seq).Middle East Respiratory Syndrome Coronavirus Intra-Host Populations Are Characterized by Numerous High Frequency Variants.Excess of mutational jackpot events in expanding populations revealed by spatial Luria-Delbrück experiments.Distinguishing low frequency mutations from RT-PCR and sequence errors in viral deep sequencing data.Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq.Ultra-deep sequencing of intra-host rabies virus populations during cross-species transmission.Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis.Ultradeep Sequencing for Detection of Quasispecies Variants in the Major Hydrophilic Region of Hepatitis B Virus in Indonesian Patients.Ultra-precise detection of mutations by droplet-based amplification of circularized DNA.Estimating Exceptionally Rare Germline and Somatic Mutation Frequencies via Next Generation Sequencing.Extremely Rare Polymorphisms in Saccharomyces cerevisiae Allow Inference of the Mutational SpectrumHighly sensitive, non-invasive detection of colorectal cancer mutations using single molecule, third generation sequencing.Using ultra-sensitive next generation sequencing to dissect DNA damage-induced mutagenesis.Genome plasticity of triple-reassortant H1N1 influenza A virus during infection of vaccinated pigs.Sendai virus intra-host population dynamics and host immunocompetence influence viral virulence during in vivo passage.Direct assessment of transcription fidelity by high-resolution RNA sequencing.Limits of neutral drift: lessons from the in vitro evolution of two ribozymes.MERIT reveals the impact of genomic context on sequencing error rate in ultra-deep applications.Subclonal mutation selection in mouse lymphomagenesis identifies known cancer loci and suggests novel candidates.
P2860
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P2860
Ultra-deep mutant spectrum profiling: improving sequencing accuracy using overlapping read pairs
description
2013 nî lūn-bûn
@nan
2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@ast
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@en
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@nl
type
label
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@ast
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@en
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@nl
prefLabel
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@ast
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@en
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@nl
P2093
P2860
P356
P1433
P1476
Ultra-deep mutant spectrum pro ...... y using overlapping read pairs
@en
P2093
Clinton Torres
Haiyin Chen-Harris
Monica K Borucki
Tom R Slezak
P2860
P356
10.1186/1471-2164-14-96
P407
P577
2013-02-12T00:00:00Z