Personalized genomic analyses for cancer mutation discovery and interpretation. - Wikidata - wikimedia - TriplyDB

Personalized genomic analyses for cancer mutation discovery and interpretation.

Personalized genomic analyses for cancer mutation discovery and interpretation.

http://www.wikidata.org/entity/Q35602861

about

Practical aspects of NGS-based pathways analysis for personalized cancer science and medicine Genomic characterization of esophageal squamous cell carcinoma: Insights from next-generation sequencing Genomic alterations in pancreatic cancer and their relevance to therapy Using large-scale genomics data to identify driver mutations in lung cancer: methods and challenges Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection Next-generation sequencing to guide cancer therapy Molecular Technologies in the Clinical Diagnostic Laboratory Integrating next-generation sequencing into clinical oncology: strategies, promises and pitfalls Circulating tumor DNA as a liquid biopsy target for detection of pancreatic cancer Validation of biomarkers to predict response to immunotherapy in cancer: Volume I - pre-analytical and analytical validation Integrating cancer genomic data into electronic health records PD-1 Blockade in Tumors with Mismatch-Repair Deficiency The next generation of metastatic melanoma: uncovering the genetic variants for anti-BRAF therapy response Real-world data in the molecular era-finding the reality in the real world.Mutation based treatment recommendations from next generation sequencing data: a comparison of web tools Data Interoperability of Whole Exome Sequencing (WES) Based Mutational Burden Estimates from Different Laboratories Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences?The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.Comparison of the seleno-transcriptome expression between human non-cancerous mammary epithelial cells and two human breast cancer cell lines Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors.Clinical Implementation of Integrated Genomic Profiling in Patients with Advanced Cancers.Genomic mutation-driven metastatic breast cancer therapy: a single center experience Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.An unusual genomic variant of pancreatic ductal adenocarcinoma with an indolent clinical course.Clinical implications of genomic alterations in the tumour and circulation of pancreatic cancer patients Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.Defining "mutation" and "polymorphism" in the era of personal genomics.Whole exome sequencing (WES) on formalin-fixed, paraffin-embedded (FFPE) tumor tissue in gastrointestinal stromal tumors (GIST).Comparison of genetic variants in matched samples using thesaurus annotation.Structure-Based Analysis Reveals Cancer Missense Mutations Target Protein Interaction Interfaces Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution Beyond genomics: critical evaluation of cell line utility for ovarian cancer research Pitfalls of improperly procured adjacent non-neoplastic tissue for somatic mutation analysis using next-generation sequencing.Clinical utility of circulating tumor DNA for molecular assessment in pancreatic cancer.Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing.Systematic Prioritization of Druggable Mutations in ∼5000 Genomes Across 16 Cancer Types Using a Structural Genomics-based Approach Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories Identification of a Novel Pathogenic Germline KDR Variant in Melanoma.The genomic landscape of response to EGFR blockade in colorectal cancer.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

http://www.wikidata.org/entity/Q35602861

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2015年论文

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name

Personalized genomic analyses for cancer mutation discovery and interpretation.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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Science Translational Medicine

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Personalized genomic analyses for cancer mutation discovery and interpretation.

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David R Riley

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P2860

Predicting deleterious amino acid substitutions

Core signaling pathways in human pancreatic cancers revealed by global genomic analyses

CDD: a Conserved Domain Database for the functional annotation of proteins

A map of human genome variation from population-scale sequencing

Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma

An integrated genomic analysis of human glioblastoma multiforme

Comprehensive molecular characterization of clear cell renal cell carcinoma.

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

Integrated genomic analyses of ovarian carcinoma

A general method applicable to the search for similarities in the amino acid sequence of two proteins

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