Whole exome capture in solution with 3 Gbp of data. - Wikidata - awgldk - TriplyDB

Whole exome capture in solution with 3 Gbp of data.

Whole exome capture in solution with 3 Gbp of data.

http://www.wikidata.org/entity/Q33610914

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A comparative analysis of exome capture Human genome sequencing in health and disease VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction Comparison of three targeted enrichment strategies on the SOLiD sequencing platform Error baseline rates of five sample preparation methods used to characterize RNA virus populations An In-Solution Hybridisation Method for the Isolation of Pathogen DNA from Human DNA-rich Clinical Samples for Analysis by NGS Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting Whole genome sequencing analysis of Plasmodium vivax using whole genome capture A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries.Transcriptome-based exon capture enables highly cost-effective comparative genomic data collection at moderate evolutionary scales.Exome sequencing in familial corticobasal degeneration Impact of the next-generation sequencing data depth on various biological result inferences.Prevention, diagnosis and treatment of high-throughput sequencing data pathologies.Impact of artifact removal on ChIP quality metrics in ChIP-seq and ChIP-exo data.Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data Large scale comparison of non-human sequences in human sequencing data.An NGS Workflow Blueprint for DNA Sequencing Data and Its Application in Individualized Molecular Oncology.Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration.De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.A method for counting PCR template molecules with application to next-generation sequencing.Targeted sequencing of the human X chromosome exome.Comprehensive assessment of sequence variation within the copy number variable defensin cluster on 8p23 by target enriched in-depth 454 sequencing.Design and development of exome capture sequencing for the domestic pig (Sus scrofa).A flexible approach for highly multiplexed candidate gene targeted resequencing.Performance comparison of exome DNA sequencing technologies.Comparison of solution-based exome capture methods for next generation sequencing Improved variant calling accuracy by merging replicates in whole-exome sequencing studies Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing.An integrative variant analysis suite for whole exome next-generation sequencing data.Exome sequencing: the sweet spot before whole genomes.Barley whole exome capture: a tool for genomic research in the genus Hordeum and beyond.Targeted capture of homoeologous coding and noncoding sequence in polyploid cotton.Analysis of hundreds of cis-regulatory landscapes at high resolution in a single, high-throughput experiment.Confidence-based somatic mutation evaluation and prioritization The uniqueome: a mappability resource for short-tag sequencing Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and Perspectives.Quantifying single nucleotide variant detection sensitivity in exome sequencing Comparison of custom capture for targeted next-generation DNA sequencing

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Whole exome capture in solution with 3 Gbp of data.

http://www.wikidata.org/entity/Q33610914

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Whole exome capture in solution with 3 Gbp of data.

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Whole exome capture in solution with 3 Gbp of data.

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Whole exome capture in solution with 3 Gbp of data.

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Whole exome capture in solution with 3 Gbp of data.

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prefLabel

Whole exome capture in solution with 3 Gbp of data.

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Whole exome capture in solution with 3 Gbp of data.

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Whole exome capture in solution with 3 Gbp of data.

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Christie Kovar

http://www.w3.org/2001/XMLSchema#string

Daniel L Burgess

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Irene Newsham

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Jacob Kitzman

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Jeffrey A Jeddeloh

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Mark D'Ascenzo

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Matthew J Rodesch

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Matthew N Bainbridge

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Min Wang

http://www.w3.org/2001/XMLSchema#string

Richard A Gibbs

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P2860

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Finding the missing heritability of complex diseases

Targeted capture and massively parallel sequencing of 12 human exomes

Fast and accurate short read alignment with Burrows-Wheeler transform

Multiplex amplification of large sets of human exons

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

Genome-wide in situ exon capture for selective resequencing

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.

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