Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
about
COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samplesWeakly positioned nucleosomes enhance the transcriptional competency of chromatinGenomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumourUltrafast and memory-efficient alignment of short DNA sequences to the human genomeEvolution of an adenocarcinoma in response to selection by targeted kinase inhibitorsChromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancerHuman genetics and genomics a decade after the release of the draft sequence of the human genomeSequence space coverage, entropy of genomes and the potential to detect non-human DNA in human samplesComputational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesTumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterationsRNA-Seq: a revolutionary tool for transcriptomicsA small-cell lung cancer genome with complex signatures of tobacco exposureinGAP-sv: a novel scheme to identify and visualize structural variation from paired end mapping dataAccurate and comprehensive sequencing of personal genomesDELLY: structural variant discovery by integrated paired-end and split-read analysisComprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomesIntegrative analysis of the melanoma transcriptomeBRAF mutations in hairy-cell leukemiaMolecular biology of lung cancer: clinical implicationsMapping copy number variation by population-scale genome sequencingTargeted capture and massively parallel sequencing of 12 human exomesMutational processes molding the genomes of 21 breast cancersA comprehensive catalogue of somatic mutations from a human cancer genomeVarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencingInitial genome sequencing and analysis of multiple myelomaMassive genomic rearrangement acquired in a single catastrophic event during cancer developmentComplex landscapes of somatic rearrangement in human breast cancer genomes.Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint libraryAccurate whole human genome sequencing using reversible terminator chemistryA universal assay for detection of oncogenic fusion transcripts by oligo microarray analysisA sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genomeChimerDB 2.0--a knowledgebase for fusion genes updatedMapping short DNA sequencing reads and calling variants using mapping quality scoresCOSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancerSequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encodingKeeping up with the next generation: massively parallel sequencing in clinical diagnosticsStatistical aspects of discerning indel-type structural variation via DNA sequence alignmentWhole-genome cancer analysis as an approach to deeper understanding of tumour biologyIdentifying fusion transcripts using next generation sequencingNew challenges for BRCA testing: a view from the diagnostic laboratory
P2860
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P2860
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Identification of somatically ...... parallel paired-end sequencing
@ast
Identification of somatically ...... parallel paired-end sequencing
@en
Identification of somatically ...... parallel paired-end sequencing
@nl
type
label
Identification of somatically ...... parallel paired-end sequencing
@ast
Identification of somatically ...... parallel paired-end sequencing
@en
Identification of somatically ...... parallel paired-end sequencing
@nl
prefLabel
Identification of somatically ...... parallel paired-end sequencing
@ast
Identification of somatically ...... parallel paired-end sequencing
@en
Identification of somatically ...... parallel paired-end sequencing
@nl
P2093
P2860
P50
P3181
P356
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P1476
Identification of somatically ...... parallel paired-end sequencing
@en
P2093
Antony Cox
Catherine Leroy
Christopher M Clee
Claire Hardy
Clive Brown
Daniel J Turner
Erin D Pleasance
Graham R Bignell
Lucy A Stebbings
Matthew E Hurles
P2860
P2888
P3181
P356
10.1038/NG.128
P407
P50
P577
2008-06-01T00:00:00Z
P5875
P6179
1047246435