about
Genetic variation in an individual human exomeMitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficienciesOptimization of de novo transcriptome assembly from next-generation sequencing dataIntegrative analysis of the melanoma transcriptomeHigh-fidelity gene synthesis by retrieval of sequence-verified DNA identified using high-throughput pyrosequencingTargeted enrichment of genomic DNA regions for next-generation sequencingEstimating the human mutation rate using autozygosity in a founder populationAccurate whole human genome sequencing using reversible terminator chemistryA comprehensive assay for targeted multiplex amplification of human DNA sequencesKeeping up with the next generation: massively parallel sequencing in clinical diagnosticsSequencing by Cyclic Ligation and Cleavage (CycLiC) directly on a microarray captured template.Massively parallel sequencing: the next big thing in genetic medicineThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceClinical implementation of comprehensive strategies to characterize cancer genomes: opportunities and challengesDental caries pathogenicity: a genomic and metagenomic perspectiveTargeted and genome-scale strategies reveal gene-body methylation signatures in human cellsMultiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersIdentification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disordersGenomic sequencing in clinical trialsIncreasing phylogenetic resolution at low taxonomic levels using massively parallel sequencing of chloroplast genomesExome sequencing of a multigenerational human pedigreeDirect multiplex sequencing (DMPS)--a novel method for targeted high-throughput sequencing of ancient and highly degraded DNASolution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencingRNA processing and its regulation: global insights into biological networksSomatic coding mutations in human induced pluripotent stem cellsAssessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy.Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology.A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries.Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencingMicrodroplet-based PCR enrichment for large-scale targeted sequencing.Fluorescent in situ sequencing (FISSEQ) of RNA for gene expression profiling in intact cells and tissues.Massively parallel exon capture and library-free resequencing across 16 genomes.A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells.Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer.Preparing a re-sequencing DNA library of 2 cancer candidate genes using the ligation-by-amplification protocol by two PCR reactions.Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection.Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.Comparison of next generation sequencing technologies for transcriptome characterization.Efficient oligonucleotide probe selection for pan-genomic tiling arrays.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Multiplex amplification of large sets of human exons
@ast
Multiplex amplification of large sets of human exons
@en
Multiplex amplification of large sets of human exons
@nl
type
label
Multiplex amplification of large sets of human exons
@ast
Multiplex amplification of large sets of human exons
@en
Multiplex amplification of large sets of human exons
@nl
prefLabel
Multiplex amplification of large sets of human exons
@ast
Multiplex amplification of large sets of human exons
@en
Multiplex amplification of large sets of human exons
@nl
P2093
P3181
P356
P1433
P1476
Multiplex amplification of large sets of human exons
@en
P2093
Bill J Peck
Christopher J Emig
Derek Austin
Emily M LeProust
Fredrik Dahl
Gregory J Porreca
Jin Billy Li
Sara L Vassallo
P2888
P3181
P356
10.1038/NMETH1110
P407
P577
2007-11-01T00:00:00Z
P5875
P6179
1045927978