Allele-specific copy number analysis of tumors. - Wikidata - awgldk - TriplyDB

Allele-specific copy number analysis of tumors.

Allele-specific copy number analysis of tumors.

http://www.wikidata.org/entity/Q34165640

about

Targeted next-generation sequencing of head and neck squamous cell carcinoma identifies novel genetic alterations in HPV+ and HPV- tumors Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone Mutational processes molding the genomes of 21 breast cancers Clonal origin and spread of metastatic prostate cancer Patterns of Chromosomal Aberrations in Solid Tumors Cancer evolution: mathematical models and computational inference SciClone: inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolution Whole-genome sequencing reveals complex mechanisms of intrinsic resistance to BRAF inhibition.SF3B1 mutations constitute a novel therapeutic target in breast cancer.Mutational signatures associated with tobacco smoking in human cancer The potential for chemical mixtures from the environment to enable the cancer hallmark of sustained proliferative signalling The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes Integrated analysis of high-resolution DNA methylation profiles, gene expression, germline genotypes and clinical end points in breast cancer patients A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders Statistical Methods in Integrative Genomics Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution Mutational signatures of ionizing radiation in second malignancies Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing Clonal Evolutionary Analysis during HER2 Blockade in HER2-Positive Inflammatory Breast Cancer: A Phase II Open-Label Clinical Trial of Afatinib +/- Vinorelbine A Biobank of Breast Cancer Explants with Preserved Intra-tumor Heterogeneity to Screen Anticancer Compounds Statistical Inference in Hidden Markov Models Using k-Segment Constraints Development of synchronous VHL syndrome tumors reveals contingencies and constraints to tumor evolution The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation The landscape of cancer genes and mutational processes in breast cancer The life history of 21 breast cancers First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation.Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization.Copynumber: Efficient algorithms for single- and multi-track copy number segmentation.Interpreting genomic data via entropic dissection.Unraveling the clonal hierarchy of somatic genomic aberrations.Bivariate segmentation of SNP-array data for allele-specific copy number analysis in tumour samples.THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data Inferring tumour purity and stromal and immune cell admixture from expression data SomatiCA: identifying, characterizing and quantifying somatic copy number aberrations from cancer genome sequencing data.An assessment of computational methods for estimating purity and clonality using genomic data derived from heterogeneous tumor tissue samples CLImAT: accurate detection of copy number alteration and loss of heterozygosity in impure and aneuploid tumor samples using whole-genome sequencing data.TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data.Inferring copy number and genotype in tumour exome data.

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P2860

Allele-specific copy number analysis of tumors.

http://www.wikidata.org/entity/Q34165640

description

2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

@wuu

name

Allele-specific copy number analysis of tumors.

@ast

Allele-specific copy number analysis of tumors.

@en

Allele-specific copy number analysis of tumors.

@nl

type

label

Allele-specific copy number analysis of tumors.

@ast

Allele-specific copy number analysis of tumors.

@en

Allele-specific copy number analysis of tumors.

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prefLabel

Allele-specific copy number analysis of tumors.

@ast

Allele-specific copy number analysis of tumors.

@en

Allele-specific copy number analysis of tumors.

@nl

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PNAS.1009843107

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Proceedings of the National Academy of Sciences of the United States of America

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Allele-specific copy number analysis of tumors.

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Anders Zetterberg

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Inga H Rye

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Peter Marynen

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Victor J Weigman

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Wei Sun

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P2860

A specific PP2A regulatory subunit, B56gamma, mediates DNA damage-induced dephosphorylation of p53 at Thr55

The tumor suppressor PP2A Abeta regulates the RalA GTPase

A small-cell lung cancer genome with complex signatures of tobacco exposure

A comprehensive catalogue of somatic mutations from a human cancer genome

Complex landscapes of somatic rearrangement in human breast cancer genomes.

Recurring mutations found by sequencing an acute myeloid leukemia genome

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications

Molecular portraits of human breast tumours

Repeated observation of breast tumor subtypes in independent gene expression data sets

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39

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107

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Anne-Lise Børresen-Dale

Charles M. Perou

Vessela Kristensen

Ole Christian Lingjærde

Silje H. Nordgard

Hege G. Russnes

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