Performance comparison of SNP detection tools with illumina exome sequencing data--an assessment using both family pedigree information and sample-matched SNP array data
about
VariantDB: a flexible annotation and filtering portal for next generation sequencing data.An NGS Workflow Blueprint for DNA Sequencing Data and Its Application in Individualized Molecular Oncology.Transcriptomic SNP discovery for custom genotyping arrays: impacts of sequence data, SNP calling method and genotyping technology on the probability of validation success.MICADo - Looking for Mutations in Targeted PacBio Cancer Data: An Alignment-Free MethodDetailed comparison of two popular variant calling packages for exome and targeted exon studiesReliably Detecting Clinically Important Variants Requires Both Combined Variant Calls and Optimized Filtering Strategies.An analytical workflow for accurate variant discovery in highly divergent regions.Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategiesTechniques and Approaches to Genetic Analyses in Nephrological Disorders.A primer on precision medicine informatics.Whole-transcriptome brain expression and exon-usage profiling in major depression and suicide: evidence for altered glial, endothelial and ATPase activity.Cross-Comparison of Exome Analysis, Next-Generation Sequencing of Amplicons, and the iPLEX(®) ADME PGx Panel for Pharmacogenomic ProfilingPEMapper and PECaller provide a simplified approach to whole-genome sequencing.Comparative analysis of SNP candidates in disparate milk yielding river buffaloes using targeted sequencing.Lightning-fast genome variant detection with GROM.Optimized Method of Extracting Rice Chloroplast DNA for High-Quality Plastome Resequencing and de Novo Assembly.A framework for the estimation of the proportion of true discoveries in single nucleotide variant detection studies for human data.Genotyping of Multiple Clinical Samples with a Combined Direct PCR and Magnetic Lateral Flow Assay
P2860
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P2860
Performance comparison of SNP detection tools with illumina exome sequencing data--an assessment using both family pedigree information and sample-matched SNP array data
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Performance comparison of SNP ...... sample-matched SNP array data
@ast
Performance comparison of SNP ...... sample-matched SNP array data
@en
type
label
Performance comparison of SNP ...... sample-matched SNP array data
@ast
Performance comparison of SNP ...... sample-matched SNP array data
@en
prefLabel
Performance comparison of SNP ...... sample-matched SNP array data
@ast
Performance comparison of SNP ...... sample-matched SNP array data
@en
P2093
P2860
P356
P1476
Performance comparison of SNP ...... sample-matched SNP array data
@en
P2093
Electron Kebebew
Robert M Stephens
Yongmei Zhao
P2860
P356
10.1093/NAR/GKU392
P407
P50
P577
2014-05-15T00:00:00Z