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The Journal of Applied Laboratory Medicine|June 28, 2019
Transplant Virus Detection Using Multiplex Targeted SequencingSusanna K Tan, Peidong Shen, Martina I Lefterova, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2013
Rare variant detection using family-based sequencing analysisGang Peng, Yu Fan, Timothy B Palculict, et al.
The Journal of Molecular Diagnostics : JMD|February 6, 2016
Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic FibrosisMartina I Lefterova, Peidong Shen, Justin I Odegaard, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2011
High-quality DNA sequence capture of 524 disease candidate genesPeidong Shen, Wenyi Wang, Sujatha Krishnakumar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2018
Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemiaGang Peng, Peidong Shen, Neeru Gandotra, et al.
Plos Computational Biology|April 25, 2009
Mapping gene associations in human mitochondria using clinical disease phenotypesCurt Scharfe, Henry Horng-Shing Lu, Jutta K Neuenburg, et al.
Proteomics|November 19, 2005
Proteome analysis of mitochondrial outer membrane from Neurospora crassaSimone Schmitt, Holger Prokisch, Tilman Schlunck, et al.
Nature Genetics|July 23, 2002
Systematic screen for human disease genes in yeastLars M Steinmetz, Curt Scharfe, Adam M Deutschbauer, et al.
The Journal of Clinical Investigation|January 5, 2023
A systems biology approach identifies the role of dysregulated PRDM6 in the development of hypertensionKushan L Gunawardhana, Lingjuan Hong, Trojan Rugira, et al.
Nucleic Acids Research|September 17, 2010
Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencingWenyi Wang, Peidong Shen, Sreedevi Thiyagarajan, et al.
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