Next Generation Sequencing for Clinical Diagnostics-Principles and Application to Targeted Resequencing for Hypertrophic Cardiomyopathy: A Paper from the 2009 William Beaumont Hosp...

von Voelkerding, Karl V., Dames, Shale, Durtschi, Jacob D.
Veröffentlicht 2010

Gene silencing in Caenorhabditis elegans by transitive RNA interference

von ALDER, MATTHEW N., DAMES, SHALE, GAUDET, JEFFREY, MANGO, SUSAN E.
Veröffentlicht 2003

Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for Resequencing of Hypertrophic Cardiomyopathy-Associated Genes

von Dames, Shale, Durtschi, Jacob, Geiersbach, Katherine, Stephens, Jack, Voelkerding, Karl V.
Veröffentlicht 2010

BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing

von Vittal, Padmaja, Hall, Deborah A, Dames, Shale, Mao, Rong, Berry‐Kravis, Elizabeth
Veröffentlicht in Mov Disord Clin Pract (2015)

Characterization of Aberrant Melting Peaks in Unlabeled Probe Assays

von Dames, Shale, Margraf, Rebecca L., Pattison, David C., Wittwer, Carl T., Voelkerding, Karl V.
Veröffentlicht 2007

A Single-Tube Nucleic Acid Extraction, Amplification, and Detection Method Using Aluminum Oxide

von Dames, Shale, Bromley, L. Kathryn, Herrmann, Mark, Elgort, Marc, Erali, Maria, Smith, Roger, Voelkerding, Karl V.
Veröffentlicht 2006

Specific versus Nonspecific Isothermal DNA Amplification through Thermophilic Polymerase and Nicking Enzyme Activities()

von Tan, Eric, Erwin, Barbara, Dames, Shale, Ferguson, Tanya, Buechel, Megan, Irvine, Bruce, Voelkerding, Karl, Niemz, Angelika
Veröffentlicht 2008

Variant Identification in Multi-Sample Pools by Illumina Genome Analyzer Sequencing

von Margraf, Rebecca L., Durtschi, Jacob D., Dames, Shale, Pattison, David C., Stephens, Jack E., Voelkerding, Karl V.
Veröffentlicht 2011

Multi-Sample Pooling and Illumina Genome Analyzer Sequencing Methods to Determine Gene Sequence Variation for Database Development

von Margraf, Rebecca L., Durtschi, Jacob D., Dames, Shale, Pattison, David C., Stephens, Jack E., Mao, Rong, Voelkerding, Karl V.
Veröffentlicht 2010

Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants

von Brunelli, Luca, Jenkins, Sabrina M., Gudgeon, James M., Bleyl, Steven B., Miller, Christine E., Tvrdik, Tatiana, Dames, Shale A., Ostrander, Betsy, Daboub, Josue A. F., Zielinski, Brandon A., Zinkhan, Erin K., Underhill, Hunter R., Wilson, Theodore, Bonkowsky, Joshua L., Yost, Christian C., Botto, Lorenzo D., Jenkins, Justin, Pysher, Theodore J., Bayrak‐Toydemir, Pinar, Mao, Rong
Veröffentlicht in Mol Genet Genomic Med (2019)