Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.
about
Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancerTargeted enrichment of genomic DNA regions for next-generation sequencingMammuthus Population Dynamics in Late Pleistocene North America: Divergence, Phylogeography, and IntrogressionA framework for variation discovery and genotyping using next-generation DNA sequencing dataEnhanced whole exome sequencing by higher DNA insert lengths.Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa.A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses.Identification of factors required for meristem function in Arabidopsis using a novel next generation sequencing fast forward genetics approach.SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers.Performance of microarray and liquid based capture methods for target enrichment for massively parallel sequencing and SNP discovery.Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing.Discovery of variants unmasked by hemizygous deletions.Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencersDevelopment of genetic markers in Eucalyptus species by target enrichment and exome sequencingGenomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsQuick, sensitive and specific detection and evaluation of quantification of minor variants by high-throughput sequencing.Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern IrelandNovel sequencing-based strategies for high-throughput discovery of genetic mutations underlying inherited antibody deficiency disordersMutation Scanning in Wheat by Exon Capture and Next-Generation Sequencing.Assessment of the latest NGS enrichment capture methods in clinical context.In vitro evolution of phi29 DNA polymerase using isothermal compartmentalized self replication technique.Next-generation genetic testing for retinitis pigmentosa.Next generation sequence analysis and computational genomics using graphical pipeline workflows.A multiplex primer design algorithm for target amplification of continuous genomic regions.Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets.Gene capture coupled to high-throughput sequencing as a strategy for targeted metagenome explorationNext generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinementsPhylOPDb: a 16S rRNA oligonucleotide probe database for prokaryotic identification.Next-generation sequencing in the clinic: promises and challenges.Genome-wide analysis of radiation-induced mutations in rice (Oryza sativa L. ssp. indica).Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.Evaluation of the evenness score in next-generation sequencing.Short read alignment with populations of genomes.A commentary on evaluation of the evenness score in next-generation sequencing.Using a priori knowledge to align sequencing reads to their exact genomic position.Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples.Inferring the evolution of the major histocompatibility complex of wild pigs and peccaries using hybridisation DNA capture-based sequencing.Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples.
P2860
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P2860
Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@ast
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@en
type
label
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@ast
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@en
prefLabel
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@ast
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@en
P2860
P50
P356
P1476
Accurate SNP and mutation dete ...... fragment sequencing libraries.
@en
P2093
Pieter J van der Zaag
P2860
P356
10.1093/NAR/GKQ072
P407
P577
2010-02-17T00:00:00Z