Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing.
about
Integrating cancer genomic data into electronic health recordsExploring Asian Indian and Pakistani views about cancer and participation in cancer genetics research: toward the development of a community genetics intervention.Genetic predisposition to hematologic malignancies: management and surveillance.Sources of discordance among germ-line variant classifications in ClinVar.The Changing Landscape of Genetic Testing for Inherited Breast Cancer Predisposition.Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer.Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.Ethical considerations surrounding germline next-generation sequencing of children with cancer.Cancer Genetic Counseling and Testing: Perspectives of Epithelial Ovarian Cancer Patients and Gynecologic Oncology Healthcare Providers.Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience.Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals.Managing Variant Interpretation Discrepancies in Hereditary Cancer: Clinical Practice, Concerns, and Desired Resources.Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.A new era in the interpretation of human genomic variation.Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts.Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach
P2860
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P2860
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@en
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@nl
type
label
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@en
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@nl
prefLabel
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@en
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@nl
P2093
P2860
P50
P356
P1476
Conflicting Interpretation of ...... Registry of Multiplex Testing.
@en
P2093
Judy E Garber
Laura Digiovanni
Mark E Robson
Michael F Walsh
Pragna Gaddam
Vijai Joseph
Zsofia K Stadler
P2860
P304
P356
10.1200/JCO.2016.68.4316
P407
P577
2016-09-12T00:00:00Z