Center-Authored Papers
Filters: Author is Salipante, Stephen J [Clear All Filters]
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2014.
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.. The Journal of molecular diagnostics : JMD. 16(1):56-67. Abstract
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2014.
Recurrent somatic loss of TNFRSF14 in classical Hodgkin lymphoma.. Genes, chromosomes & cancer. Abstract
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2015.
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2013.
Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strains.. Genome research. 25(1):119-28. Abstract
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2015.
Incidental identification of Strongyloides stercoralis infection by broad-range 28S rDNA gene sequencing in a patient with a hematolymphoid malignancy.. Diagnostic microbiology and infectious disease. 86(4):362-364. Abstract
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2016.
Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers.. Proceedings of the National Academy of Sciences of the United States of America. 108(41):17087-92. Abstract
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2011.
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2015.
Detection of minimal residual disease in NPM1-mutated acute myeloid leukemia by next-generation sequencing.. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. Abstract
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2014.
Clonal expansions in ulcerative colitis identify patients with neoplasia.. Proceedings of the National Academy of Sciences of the United States of America. 106(49):20871-6. Abstract
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2009.
Characterization of a multidrug-resistant, novel Bacteroides genomospecies.. Emerging infectious diseases. 21(1):95-8. Abstract
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2015. Doing Business with Arnold Library
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