Performance comparison of four exome capture systems for deep sequencing. - Wikidata - awgldk - TriplyDB

Performance comparison of four exome capture systems for deep sequencing.

Performance comparison of four exome capture systems for deep sequencing.

http://www.wikidata.org/entity/Q35184230

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Next generation sequencing technology and genomewide data analysis: Perspectives for retinal research Novel Approaches for Fungal Transcriptomics from Host Samples Integrating next-generation sequencing into clinical oncology: strategies, promises and pitfalls Genome Analysis of Osteosarcoma Progression Samples Identifies FGFR1 Overexpression as a Potential Treatment Target and CHM as a Candidate Tumor Suppressor Gene Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency.Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity.The use of next-generation sequencing in molecular diagnosis of neurofibromatosis type 1: a validation study.Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing Performance comparison of four commercial human whole-exome capture platforms Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling New insights into the performance of human whole-exome capture platforms.Ultraconserved Elements Sequencing as a Low-Cost Source of Complete Mitochondrial Genomes and Microsatellite Markers in Non-Model Amniotes.Exome Capture with Heterologous Enrichment in Pig (Sus scrofa)What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?Reliably Detecting Clinically Important Variants Requires Both Combined Variant Calls and Optimized Filtering Strategies.Integrating 400 million variants from 80,000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts.Assessment of the latest NGS enrichment capture methods in clinical context.Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.The minimal amount of starting DNA for Agilent's hybrid capture-based targeted massively parallel sequencing Exon capture optimization in amphibians with large genomes.MTTE: an innovative strategy for the evaluation of targeted/exome enrichment efficiency Performance comparison of two commercial human whole-exome capture systems on formalin-fixed paraffin-embedded lung adenocarcinoma samples.AlignerBoost: A Generalized Software Toolkit for Boosting Next-Gen Sequencing Mapping Accuracy Using a Bayesian-Based Mapping Quality Framework.Retinal Diseases Caused by Mutations in Genes Not Specifically Associated with the Clinical Diagnosis Use of liquid biopsies to monitor disease progression in a sarcoma patient: a case report.Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.A computational method for estimating the PCR duplication rate in DNA and RNA-seq experiments.Targeted sequencing of both DNA strands barcoded and captured individually by RNA probes to identify genome-wide ultra-rare mutations.Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies Orthogonal NGS for High Throughput Clinical Diagnostics.Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders Sequence capture by hybridization to explore modern and ancient genomic diversity in model and nonmodel organisms.The Qatar genome: a population-specific tool for precision medicine in the Middle East Bisulfite oligonucleotide-capture sequencing for targeted base- and strand-specific absolute 5-methylcytosine quantitation.Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer.Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.Preclinical evaluation of potential therapeutic targets in dedifferentiated liposarcoma.Whole genome/exome sequencing in mood and psychotic disorders.

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Performance comparison of four exome capture systems for deep sequencing.

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2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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name

Performance comparison of four exome capture systems for deep sequencing.

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Performance comparison of four exome capture systems for deep sequencing.

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type

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Performance comparison of four exome capture systems for deep sequencing.

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Performance comparison of four exome capture systems for deep sequencing.

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Performance comparison of four exome capture systems for deep sequencing.

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Performance comparison of four exome capture systems for deep sequencing.

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Performance comparison of four exome capture systems for deep sequencing.

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Chandra Sekhar Reddy Chilamakuri

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Jinchang Sun

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Leonardo A Meza-Zepeda

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Mohammed-Amin Madoui

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Susanne Lorenz

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A comparative analysis of exome capture

Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A

Genomewide comparison of DNA sequences between humans and chimpanzees

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

Genome-wide in situ exon capture for selective resequencing

Using whole-exome sequencing to identify inherited causes of autism.

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