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American Journal of Human Genetics|October 13, 2006
Detecting disease-causing mutations in the human genome by haplotype matchingDavid H Spencer, Kerry L Bubb, Maynard V OlsonAmerican Journal of Clinical Pathology|October 28, 2011
Validation and implementation of the GeneXpert MRSA/SA blood culture assay in a pediatric settingDavid H Spencer, Patricia Sellenriek, Carey-Ann D BurnhamLeukemia|May 14, 2020
Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cellsReza Ghasemi, Heidi Struthers, Elisabeth R Wilson, et al.Journal of Bacteriology|March 4, 2005
Evidence for diversifying selection at the pyoverdine locus of Pseudomonas aeruginosaEric E Smith, Elizabeth H Sims, David H Spencer, et al.Human Mutation|April 26, 2022
Clinical whole-genome sequencing in cancer diagnosisYing-Chen C Hou, Julie A Neidich, Eric J Duncavage, et al.The Journal of Molecular Diagnostics : JMD|July 2, 2013
Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimensDavid H Spencer, Jennifer K Sehn, Haley J Abel, et al.Blood Advances|January 25, 2018
Expression profiling of snoRNAs in normal hematopoiesis and AMLWayne A Warner, David H Spencer, Maria Trissal, et al.The Journal of Molecular Diagnostics : JMD|November 12, 2013
Performance of common analysis methods for detecting low-frequency single nucleotide variants in targeted next-generation sequence dataDavid H Spencer, Manoj Tyagi, Francesco Vallania, et al.Aesthetic Surgery Journal|November 9, 2022
Evaluation of Breast Implant-Associated Anaplastic Large Cell Lymphoma With Whole Exome and Genome SequencingNeha Akkad, Rohan Kodgule, Eric J Duncavage, et al.American Journal of Clinical Pathology|September 20, 2015
Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing TestingJennifer K Sehn, David H Spencer, John D Pfeifer, et al.Pageof 5