Quantification of rare allelic variants from pooled genomic DNA
about
Sequencing pools of individuals — mining genome-wide polymorphism data without big fundingApplication of large-scale sequencing to marker discovery in plantsHigh-throughput sequencing and mutagenesis to accelerate the domestication of Microlaena stipoides as a new food cropRare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease familiesEfficient and cost effective population resequencing by pooling and in-solution hybridizationThe Future of Children's Health in the Genomic EraSomatic coding mutations in human induced pluripotent stem cellsDetection and quantification of rare mutations with massively parallel sequencing.Estimation of population allele frequencies from next-generation sequencing data: pool-versus individual-based genotyping.Estimating DNA polymorphism from next generation sequencing data with high error rate by dual sequencing applications.Coval: improving alignment quality and variant calling accuracy for next-generation sequencing data.PoPoolation: a toolbox for population genetic analysis of next generation sequencing data from pooled individualsThe PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriersThe next generation of complex lung genetic studies.Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instabilityCardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with diseaseDesign of association studies with pooled or un-pooled next-generation sequencing data.Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.High-throughput discovery of rare insertions and deletions in large cohortsDeep sequencing of the Nicastrin gene in pooled DNA, the identification of genetic variants that affect risk of Alzheimer's disease.Discovery of rare mutations in populations: TILLING by sequencing.Resequencing of pooled DNA for detecting disease associations with rare variants.A statistical method for the detection of variants from next-generation resequencing of DNA pools.Two evolutionary histories in the genome of rice: the roles of domestication genesStatistical mutation calling from sequenced overlapping DNA pools in TILLING experiments.SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data.Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database developmentAnalysis and optimal design for association studies using next-generation sequencing with case-control pools.COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing.Determination of RET Sequence Variation in an MEN2 Unaffected Cohort Using Multiple-Sample Pooling and Next-Generation SequencingA new approach for detecting low-level mutations in next-generation sequence data.Detection of ultra-rare mutations by next-generation sequencing.Detection of rare genomic variants from pooled sequencing using SPLINTER.Empirical validation of pooled whole genome population re-sequencing in Drosophila melanogasterSIMPLEX: cloud-enabled pipeline for the comprehensive analysis of exome sequencing data.Confidence-based somatic mutation evaluation and prioritizationInvestigations into genome diversity of Haemophilus influenzae using whole genome sequencing of clinical isolates and laboratory transformantsPopulation-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexingA unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms.
P2860
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P2860
Quantification of rare allelic variants from pooled genomic DNA
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին 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
Quantification of rare allelic variants from pooled genomic DNA
@ast
Quantification of rare allelic variants from pooled genomic DNA
@en
Quantification of rare allelic variants from pooled genomic DNA
@nl
type
label
Quantification of rare allelic variants from pooled genomic DNA
@ast
Quantification of rare allelic variants from pooled genomic DNA
@en
Quantification of rare allelic variants from pooled genomic DNA
@nl
prefLabel
Quantification of rare allelic variants from pooled genomic DNA
@ast
Quantification of rare allelic variants from pooled genomic DNA
@en
Quantification of rare allelic variants from pooled genomic DNA
@nl
P2093
P2860
P50
P356
P1433
P1476
Quantification of rare allelic variants from pooled genomic DNA
@en
P2093
Aaron Hamvas
Daniel J Wegner
Francesco L M Vallania
Jacqueline A Bonds
Olivia L Knowles
Sarah W Robison
Scott W Doniger
P2860
P2888
P304
P356
10.1038/NMETH.1307
P577
2009-03-01T00:00:00Z
P5875
P6179
1004412748