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Times Cited: 55
Times Cited
Times Co-cited
Similarity
Signatures of mutational processes in human cancer.
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Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth.
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Ahmet Zehir, Ryma Benayed, Ronak H Shah, Aijazuddin Syed, Sumit Middha, Hyunjae R Kim, Preethi Srinivasan, Jianjiong Gao, Debyani Chakravarty, Sean M Devlin,[...]. Nat Med 2017
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Feasibility of Large-Scale Genomic Testing to Facilitate Enrollment Onto Genomically Matched Clinical Trials.
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The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data.
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Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.
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The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
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High-Throughput Genomics and Clinical Outcome in Hard-to-Treat Advanced Cancers: Results of the MOSCATO 01 Trial.
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Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study.
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Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
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Integrated genomic characterization of endometrial carcinoma.
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dbSNP: the NCBI database of genetic variation.
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COSMIC: exploring the world's knowledge of somatic mutations in human cancer.
Simon A Forbes, David Beare, Prasad Gunasekaran, Kenric Leung, Nidhi Bindal, Harry Boutselakis, Minjie Ding, Sally Bamford, Charlotte Cole, Sari Ward,[...]. Nucleic Acids Res 2015
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A framework for variation discovery and genotyping using next-generation DNA sequencing data.
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SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data.
Zhongyang Zhang, Ke Hao. PLoS Comput Biol 2015
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VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.
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Analysis of protein-coding genetic variation in 60,706 humans.
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The Sequence Alignment/Map format and SAMtools.
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Impact of Precision Medicine in Diverse Cancers: A Meta-Analysis of Phase II Clinical Trials.
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Molecularly targeted therapy based on tumour molecular profiling versus conventional therapy for advanced cancer (SHIVA): a multicentre, open-label, proof-of-concept, randomised, controlled phase 2 trial.
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Integrating next-generation sequencing into clinical oncology: strategies, promises and pitfalls.
Peter Horak, Stefan Fröhling, Hanno Glimm. ESMO Open 2016
Peter Horak, Stefan Fröhling, Hanno Glimm. ESMO Open 2016
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First-line crizotinib versus chemotherapy in ALK-positive lung cancer.
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Integrative clinical genomics of metastatic cancer.
Dan R Robinson, Yi-Mi Wu, Robert J Lonigro, Pankaj Vats, Erin Cobain, Jessica Everett, Xuhong Cao, Erica Rabban, Chandan Kumar-Sinha, Victoria Raymond,[...]. Nature 2017
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Development and validation of a scalable next-generation sequencing system for assessing relevant somatic variants in solid tumors.
Daniel H Hovelson, Andrew S McDaniel, Andi K Cani, Bryan Johnson, Kate Rhodes, Paul D Williams, Santhoshi Bandla, Geoffrey Bien, Paul Choppa, Fiona Hyland,[...]. Neoplasia 2015
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High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing.
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The human genome browser at UCSC.
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Coming of age: ten years of next-generation sequencing technologies.
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Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.
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GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers.
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5
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.