Massively parallel exon capture and library-free resequencing across 16 genomes.
about
Analysis of the genome to personalize therapy for melanomaTargeted capture and massively parallel sequencing of 12 human exomesTargeted enrichment of genomic DNA regions for next-generation sequencingEstimating the human mutation rate using autozygosity in a founder populationCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesMassively parallel sequencing: the new frontier of hematologic genomicsSuccesses and challenges of using whole exome sequencing to identify novel genes underlying an inherited predisposition for thoracic aortic aneurysms and acute aortic dissectionsThe promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disordersMultiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersNext-generation genomics: an integrative approachPooled association tests for rare variants in exon-resequencing studiesSporadic autism exomes reveal a highly interconnected protein network of de novo mutationsAccurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.Microdroplet-based PCR enrichment for large-scale targeted sequencing.Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts.Whole-genome sequencing of a laboratory-evolved yeast strain.Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process.SNP identification, verification, and utility for population genetics in a non-model genusTargeted enrichment of specific regions in the human genome by array hybridization.Targeted resequencing of candidate genes using selector probes.Combining target enrichment with barcode multiplexing for high throughput SNP discoveryPenalized regression for genome-wide association screening of sequence dataMultiplex target enrichment using DNA indexing for ultra-high throughput SNP detection.A genotype-first approach to defining the subtypes of a complex diseaseTargeted Capture and High-Throughput Sequencing Using Molecular Inversion Probes (MIPs)Targeted deep resequencing of the human cancer genome using next-generation technologies.Genomic approaches for the discovery of genes mutated in inherited retinal degeneration.The genetic variability and commonality of neurodevelopmental disease.Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencing.Addressing challenges in the production and analysis of illumina sequencing dataHighly-multiplexed barcode sequencing: an efficient method for parallel analysis of pooled samples.Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthmaTargeted sequencing library preparation by genomic DNA circularization.Library-free methylation sequencing with bisulfite padlock probes.Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.New technologies for the identification of novel genetic markers of disorders of sex development (DSD).Emergence of single-molecule sequencing and potential for molecular diagnostic applications.Development of genomic resources for Pacific Herring through targeted transcriptome pyrosequencingSynteny-based mapping-by-sequencing enabled by targeted enrichment.Exome sequencing: the sweet spot before whole genomes.
P2860
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P2860
Massively parallel exon capture and library-free resequencing across 16 genomes.
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Massively parallel exon capture and library-free resequencing across 16 genomes.
@ast
Massively parallel exon capture and library-free resequencing across 16 genomes.
@en
type
label
Massively parallel exon capture and library-free resequencing across 16 genomes.
@ast
Massively parallel exon capture and library-free resequencing across 16 genomes.
@en
prefLabel
Massively parallel exon capture and library-free resequencing across 16 genomes.
@ast
Massively parallel exon capture and library-free resequencing across 16 genomes.
@en
P2093
P2860
P356
P1433
P1476
Massively parallel exon capture and library-free resequencing across 16 genomes.
@en
P2093
Deborah A Nickerson
Sarah B Ng
P2860
P2888
P304
P356
10.1038/NMETH.F.248
P577
2009-04-06T00:00:00Z
P5875
P6179
1014925042