Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. - Wikidata - wikimedia - TriplyDB

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

http://www.wikidata.org/entity/Q34327021

about

Mutational heterogeneity in cancer and the search for new cancer-associated genes Somatic mutations in disorders with disrupted brain connectivity Practical aspects of NGS-based pathways analysis for personalized cancer science and medicine Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection Somatic mosaicism in the human genome Massively parallel sequencing: the new frontier of hematologic genomics Three-stage quality control strategies for DNA re-sequencing data Cancer evolution: mathematical models and computational inference Recurrent SMARCA4 mutations in small cell carcinoma of the ovary.Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.Resistance mechanisms for the Bruton's tyrosine kinase inhibitor ibrutinib Convergent loss of PTEN leads to clinical resistance to a PI(3)Kα inhibitor.Unique genomic profile of fibrolamellar hepatocellular carcinoma.Integrative clinical genomics of advanced prostate cancer.Technological considerations for genome-guided diagnosis and management of cancer Integrating next-generation sequencing into clinical oncology: strategies, promises and pitfalls Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations Computational characterisation of cancer molecular profiles derived using next generation sequencing Comprehensive molecular profiling of lung adenocarcinoma.Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes Mutational landscape and significance across 12 major cancer types Discovery and saturation analysis of cancer genes across 21 tumour types Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas Comprehensive molecular characterization of urothelial bladder carcinoma Age-related clonal hematopoiesis associated with adverse outcomes Elucidating Genomic Characteristics of Lung Cancer Progression from In Situ to Invasive Adenocarcinoma Single-cell transcriptogenomics reveals transcriptional exclusion of ENU-mutated alleles Subtyping sub-Saharan esophageal squamous cell carcinoma by comprehensive molecular analysis Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals Notch pathway activation is essential for maintenance of stem-like cells in early tongue cancer Global Analysis of the Fungal Microbiome in Cystic Fibrosis Patients Reveals Loss of Function of the Transcriptional Repressor Nrg1 as a Mechanism of Pathogen Adaptation Genome Analysis of Osteosarcoma Progression Samples Identifies FGFR1 Overexpression as a Potential Treatment Target and CHM as a Candidate Tumor Suppressor Gene Clonal Evolutionary Analysis during HER2 Blockade in HER2-Positive Inflammatory Breast Cancer: A Phase II Open-Label Clinical Trial of Afatinib +/- Vinorelbine RNA2DNAlign: nucleotide resolution allele asymmetries through quantitative assessment of RNA and DNA paired sequencing data Control for stochastic sampling variation and qualitative sequencing error in next generation sequencing Intra-tumor genetic heterogeneity and mortality in head and neck cancer: analysis of data from the Cancer Genome Atlas Bionimbus: a cloud for managing, analyzing and sharing large genomics datasets BAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity.

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Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

http://www.wikidata.org/entity/Q34327021

description

2013 nî lūn-bûn

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2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2013 թվականի փետրվարին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Sensitive detection of somatic ...... heterogeneous cancer samples.

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Sensitive detection of somatic ...... heterogeneous cancer samples.

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Sensitive detection of somatic ...... heterogeneous cancer samples.

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Nature Biotechnology

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Sensitive detection of somatic ...... heterogeneous cancer samples.

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Andrey Sivachenko

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David Jaffe

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Michael S Lawrence

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Scott L Carter

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P2860

A landscape of driver mutations in melanoma

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

dbSNP: the NCBI database of genetic variation

Melanoma genome sequencing reveals frequent PREX2 mutations

Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas

International network of cancer genome projects.

Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

A map of human genome variation from population-scale sequencing

The genomic complexity of primary human prostate cancer

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213-219

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10.1038/NBT.2514

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3

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31

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Kristian Cibulskis

Matthew Meyerson

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2013-02-10T00:00:00Z

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235441453

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3833702

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