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Human genetics and genomics a decade after the release of the draft sequence of the human genomeData-independent proteomic screen identifies novel tamoxifen agonist that mediates drug resistanceAssessing the Costs and Cost-Effectiveness of Genomic SequencingCancer Metabolism and Drug ResistanceNext-Generation Sequencing in Clinical Molecular Diagnostics of Cancer: Advantages and ChallengesTranslation of genomics-guided RNA-based personalised cancer vaccines: towards the bedsideToward precision medicine of breast cancerReinventing diagnostics for personalized therapy in oncologySimple and efficient methods for enrichment and isolation of endonuclease modified cellsDeriving a mutation index of carcinogenicity using protein structure and protein interfacesBAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity.Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debateHybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue.Measuring differential gene expression with RNA-seq: challenges and strategies for data analysis.CopywriteR: DNA copy number detection from off-target sequence dataIntersect-then-combine approach: improving the performance of somatic variant calling in whole exome sequencing data using multiple aligners and callers.Biochemical, cellular, and biophysical characterization of a potent inhibitor of mutant isocitrate dehydrogenase IDH1.Rate, molecular spectrum, and consequences of human mutationSimulated annealing based algorithm for identifying mutated driver pathways in cancerGenetics and epigenetics of the skin meet deep sequence.Gene network-based analysis identifies two potential subtypes of small intestinal neuroendocrine tumors.Applications of the human p53 knock-in (Hupki) mouse model for human carcinogen testing.Novel molecular and computational methods improve the accuracy of insertion site analysis in Sleeping Beauty-induced tumors.A systematic approach to identify novel cancer drug targets using machine learning, inhibitor design and high-throughput screening.VarSifter: visualizing and analyzing exome-scale sequence variation data on a desktop computerJointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data.Reconstructing cancer genomes from paired-end sequencing dataRNA-Seq and human complex diseases: recent accomplishments and future perspectives.A large-scale RNAi-based mouse tumorigenesis screen identifies new lung cancer tumor suppressors that repress FGFR signalingA survey of tools for variant analysis of next-generation genome sequencing data.Phred-Phrap package to analyses tools: a pipeline to facilitate population genetics re-sequencing studies.Automated analysis of immunohistochemistry images identifies candidate location biomarkers for cancers.Tumorspheres but not adherent cells derived from retinoblastoma tumors are of malignant origin.Microenvironmental genomic alterations reveal signaling networks for head and neck squamous cell carcinoma.Mouse Tumor Biology (MTB): a database of mouse models for human cancerDe novo discovery of mutated driver pathways in cancerExpression of the Long Non-Coding RNA HOTAIR Correlates with Disease Progression in Bladder Cancer and Is Contained in Bladder Cancer Patient Urinary ExosomesIdentifying micro-inversions using high-throughput sequencing readsIntegrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancerA comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Cancer genome sequencing: a review.
@en
Cancer genome sequencing: a review.
@nl
type
label
Cancer genome sequencing: a review.
@en
Cancer genome sequencing: a review.
@nl
prefLabel
Cancer genome sequencing: a review.
@en
Cancer genome sequencing: a review.
@nl
P2860
P356
P1476
Cancer genome sequencing: a review.
@en
P2093
Elaine R Mardis
Richard K Wilson
P2860
P304
P356
10.1093/HMG/DDP396
P577
2009-10-01T00:00:00Z