Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study. - Test2 - elhamkhani - TriplyDB

Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.

Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.

http://www.wikidata.org/entity/Q31157014

about

DNA Repair Pathway Alterations in Bladder Cancer.A regulation probability model-based meta-analysis of multiple transcriptomics data sets for cancer biomarker identification.Resources for Interpreting Variants in Precision Genomic Oncology Applications.Interactive or static reports to guide clinical interpretation of cancer genomics.Multicenter validation of cancer gene panel-based next-generation sequencing for translational research and molecular diagnostics.An integrated clinical and genomic information system for cancer precision medicine.Inherited DNA-Repair Defects in Colorectal Cancer.Clinical exome sequencing in France and Quebec: what are the challenges? What does the future hold?Adaptively capturing the heterogeneity of expression for cancer biomarker identification

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P2860

Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.

http://www.wikidata.org/entity/Q31157014

description

2017 nî lūn-bûn

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2017 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2017 թվականի հունվարին հրատարակված գիտական հոդված

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2017年の論文

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2017年学术文章

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2017年学术文章

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Carrie Cibulskis

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Christine A Lydon

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Elaine Hiller

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P2860

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.

Discovery and saturation analysis of cancer genes across 21 tumour types

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing

Clinical analysis and interpretation of cancer genome data

Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.

Personalized oncology through integrative high-throughput sequencing: a pilot study.

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

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787-795

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10.1038/GIM.2016.191

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Steven M Corsello

Arezou A Ghazani

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Joseph P St Pierre

Andrea Garofalo

Irene R Rainville

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