Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications.
about
Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvementMoving towards causality in attention-deficit hyperactivity disorder: overview of neural and genetic mechanismsSeqHBase: a big data toolset for family based sequencing data analysisIdentifying disease mutations in genomic medicine settings: current challenges and how to accelerate progressWhole-genome sequencing in an autism multiplex familyAnalysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder.WEP: a high-performance analysis pipeline for whole-exome data.SeqMule: automated pipeline for analysis of human exome/genome sequencing dataMolecular genetic testing and the future of clinical genomics.Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected?The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans.Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing.The impact of genomics on pediatric research and medicine.Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis.Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia.Applications of high-throughput DNA sequencing to benign hematologyVariant Ranker: a web-tool to rank genomic data according to functional significance.Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing.Incidental findings from clinical sequencing in Greece: reporting experts' attitudes.Clinical relevance of cancer genome sequencing.Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder.
P2860
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P2860
Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Exome sequencing and unrelated ...... cal and clinical implications.
@ast
Exome sequencing and unrelated ...... cal and clinical implications.
@en
type
label
Exome sequencing and unrelated ...... cal and clinical implications.
@ast
Exome sequencing and unrelated ...... cal and clinical implications.
@en
prefLabel
Exome sequencing and unrelated ...... cal and clinical implications.
@ast
Exome sequencing and unrelated ...... cal and clinical implications.
@en
P2093
P2860
P1433
P1476
Exome sequencing and unrelated ...... cal and clinical implications.
@en
P2093
Barry Moore
Fred Reimherr
Gholson J Lyon
Hakon Hakonarson
Jinchuan Xing
Joseph T Glessner
Josephine Elia
Lifeng Tian
P2860
P577
2011-07-01T00:00:00Z