A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
about
Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq ConsortiumAssessing the Costs and Cost-Effectiveness of Genomic SequencingIncidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeAn eMERGE Clinical Center at Partners Personalized MedicineAre physicians prepared for whole genome sequencing? a qualitative analysisPsychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq projectA survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.The DNA Bank: High-Security Bank Accounts to Protect and Share Your Genetic Identity.Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized Medicine.Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?Genomic sequencing in clinical practice: applications, challenges, and opportunities.How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.Prospective functional classification of all possible missense variants in PPARG.Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.My46: a Web-based tool for self-guided management of genomic test results in research and clinical settingsHealth Care Infrastructure for Financially Sustainable Clinical Genomics.Clinical exome sequencing reports: current informatics practice and future opportunities.Design of a randomized controlled trial for genomic carrier screening in healthy patients seeking preconception genetic testing.Sequencing-based diagnostics for pediatric genetic diseases: progress and potentialAggregate penetrance of genomic variants for actionable disorders in European and African Americans.Critical points for an accurate human genome analysis.User-centered design of multi-gene sequencing panel reports for clinicians.Returning pharmacogenetic secondary findings from genome sequencing: let's not put the cart before the horse.A curated gene list for reporting results of newborn genomic sequencing.Interactive or static reports to guide clinical interpretation of cancer genomics.A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation.The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.Communication challenges for nongeneticist physicians relaying clinical genomic results.Management of Incidental Findings in Clinical Genomic Sequencing.Which attributes of whole genome sequencing tests are most important to the general population? Results from a German preference study.Enhancing genomic laboratory reports: A qualitative analysis of provider review.The BabySeq project: implementing genomic sequencing in newborns
P2860
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P2860
A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին 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
A systematic approach to the r ...... from whole genome sequencing.
@ast
A systematic approach to the r ...... from whole genome sequencing.
@en
type
label
A systematic approach to the r ...... from whole genome sequencing.
@ast
A systematic approach to the r ...... from whole genome sequencing.
@en
prefLabel
A systematic approach to the r ...... from whole genome sequencing.
@ast
A systematic approach to the r ...... from whole genome sequencing.
@en
P2093
P2860
P50
P1433
P1476
A systematic approach to the r ...... from whole genome sequencing.
@en
P2093
Calum A MacRae
Christine E Seidman
Danielle R Azzariti
Denise Lautenbach
Heather M McLaughlin
Jason L Vassy
Joel Krier
Kalotina Machini
MedSeq Project
Michael F Murray
P2860
P2888
P356
10.1186/S12881-014-0134-1
P577
2014-12-14T00:00:00Z
P5875
P6179
1016016869