Detection of ultra-rare mutations by next-generation sequencing. - Test2 - elhamkhani - TriplyDB

Detection of ultra-rare mutations by next-generation sequencing.

Detection of ultra-rare mutations by next-generation sequencing.

http://www.wikidata.org/entity/Q34291814

about

Single cell genomics: advances and future perspectives Rational Protein Engineering Guided by Deep Mutational Scanning The influence of subclonal resistance mutations on targeted cancer therapy Best practices for evaluating single nucleotide variant calling methods for microbial genomics Lost in transcription: transient errors in information transfer Deciphering intratumor heterogeneity and temporal acquisition of driver events to refine precision medicine Massively parallel sequencing: the new frontier of hematologic genomics Do mutator mutations fuel tumorigenesis?Breast cancer intra-tumor heterogeneity High-throughput sequencing in mitochondrial DNA research Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress Current developments in molecular monitoring in chronic myeloid leukemia Changing genetic paradigms: creating next-generation genetic databases as tools to understand the emerging complexities of genotype/phenotype relationships Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues Deep sequencing of protease inhibitor resistant HIV patient isolates reveals patterns of correlated mutations in Gag and protease Modified Proofreading PCR for Detection of Point Mutations, Insertions and Deletions Using a ddNTP-Blocked Primer Detection of Low-Level Mixed-Population Drug Resistance in Mycobacterium tuberculosis Using High Fidelity Amplicon Sequencing Genome-Wide Estimation of the Spontaneous Mutation Rate of Human Adenovirus 5 by High-Fidelity Deep Sequencing Control for stochastic sampling variation and qualitative sequencing error in next generation sequencing Exome-wide somatic microsatellite variation is altered in cells with DNA repair deficiencies Mutational spectra of aflatoxin B1 in vivo establish biomarkers of exposure for human hepatocellular carcinoma.High-throughput profiling of point mutations across the HIV-1 genome.Detecting ultralow-frequency mutations by Duplex Sequencing.SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing.Characterizing Benzo[a]pyrene-induced lacZ mutation spectrum in transgenic mice using next-generation sequencing.Quantitative identification of mutant alleles derived from lung cancer in plasma cell-free DNA via anomaly detection using deep sequencing data.Degenerate adaptor sequences for detecting PCR duplicates in reduced representation sequencing data improve genotype calling accuracy.Streamlined analysis of duplex sequencing data with Du Novo.Development and validation of a clinical trial patient stratification assay that interrogates 27 mutation sites in MAPK pathway genes.αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia.Comprehensive evaluation and optimization of amplicon library preparation methods for high-throughput antibody sequencing Modeling Tumor Clonal Evolution for Drug Combinations Design An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage.Rational design of non-resistant targeted cancer therapies Asymmetrical barcode adapter-assisted recovery of duplicate reads and error correction strategy to detect rare mutations in circulating tumor DNA.A 'Semi-Protected Oligonucleotide Recombination' Assay for DNA Mismatch Repair in vivo Suggests Different Modes of Repair for Lagging Strand Mismatches.MAGERI: Computational pipeline for molecular-barcoded targeted resequencing.A high-throughput assay for quantitative measurement of PCR errors.Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq.High-resolution quantification of hepatitis C virus genome-wide mutation load and its correlation with the outcome of peginterferon-alpha2a and ribavirin combination therapy

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Detection of ultra-rare mutations by next-generation sequencing.

http://www.wikidata.org/entity/Q34291814

description

2012 nî lūn-bûn

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2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Detection of ultra-rare mutations by next-generation sequencing.

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Detection of ultra-rare mutations by next-generation sequencing.

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Detection of ultra-rare mutations by next-generation sequencing.

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type

label

Detection of ultra-rare mutations by next-generation sequencing.

@ast

Detection of ultra-rare mutations by next-generation sequencing.

@en

Detection of ultra-rare mutations by next-generation sequencing.

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prefLabel

Detection of ultra-rare mutations by next-generation sequencing.

@ast

Detection of ultra-rare mutations by next-generation sequencing.

@en

Detection of ultra-rare mutations by next-generation sequencing.

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PNAS.1208715109

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Detection of ultra-rare mutations by next-generation sequencing.

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P2093

Edward J Fox

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Jesse J Salk

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Joseph B Hiatt

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Lawrence A Loeb

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Michael W Schmitt

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Scott R Kennedy

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P2860

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Embryonic stem cells and somatic cells differ in mutation frequency and type

Hypervariable sites in the mtDNA control region are mutational hotspots

Circulating microRNAs as stable blood-based markers for cancer detection.

A large genome center's improvements to the Illumina sequencing system.

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

Somatic mutations in aging, cancer and neurodegeneration

Quality control by DNA repair

Fragmentation of contaminant and endogenous DNA in ancient samples determined by shotgun sequencing; prospects for human palaeogenomics

Ultra-deep sequencing of foraminiferal microbarcodes unveils hidden richness of early monothalamous lineages in deep-sea sediments.

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14508-14513

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