Measures of Clade Confidence Do Not Correlate with Accuracy of Phylogenetic Trees

por Hall, Barry G, Salipante, Stephen J
Publicado 2007

Retraction: Measures of Clade Confidence Do Not Correlate with Accuracy of Phylogenetic Trees

por Hall, Barry G, Salipante, Stephen J
Publicado 2007

PeakSeeker: a program for interpreting genotypes of mononucleotide repeats

por Thompson, James M, Salipante, Stephen J
Publicado 2009

16S rRNA deep sequencing identifies Actinotignum schaalii as the major component of a polymicrobial intra-abdominal infection and implicates a urinary source

por Bryan, Andrew, Kirkpatrick, Lindsey M., Manaloor, John J., Salipante, Stephen J.
Publicado 2017

Ultrasensitive detection of acute myeloid leukemia minimal residual disease using single molecule molecular inversion probes

por Waalkes, Adam, Penewit, Kelsi, Wood, Brent L., Wu, David, Salipante, Stephen J.
Publicado 2017

1190. Dual-Plasmid Technology for Precision Genome Editing in Staphylococcus aureus

por Reish, Jennifer, Dey, Somrita, Penewit, Kelsi, Salipante, Stephen J, Berti, Andrew David
Publicado 2020

Detection of minimal residual disease in NPM1-mutated acute myeloid leukemia by next-generation sequencing

por Salipante, Stephen J., Fromm, Jonathan R., Shendure, Jay, Wood, Brent L., Wu, David
Publicado 2014

Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation

por Hiatt, Joseph B., Pritchard, Colin C., Salipante, Stephen J., O'Roak, Brian J., Shendure, Jay
Publicado 2013

Efficient and Scalable Precision Genome Editing in Staphylococcus aureus through Conditional Recombineering and CRISPR/Cas9-Mediated Counterselection

por Penewit, Kelsi, Holmes, Elizabeth A., McLean, Kathyrn, Ren, Mingxin, Waalkes, Adam, Salipante, Stephen J.
Publicado 2018

Erratum for Penewit et al., “Efficient and Scalable Precision Genome Editing in Staphylococcus aureus through Conditional Recombineering and CRISPR/Cas9-Mediated Counterselection”...

por Penewit, Kelsi, Holmes, Elizabeth A., McLean, Kathryn, Ren, Mingxin, Waalkes, Adam, Salipante, Stephen J.
Publicado 2018

Erratum for Penewit et al., “Efficient and Scalable Precision Genome Editing in Staphylococcus aureus through Conditional Recombineering and CRISPR/Cas9-Mediated Counterselection”...

por Penewit, Kelsi, Holmes, Elizabeth A., McLean, Kathryn, Ren, Mingxin, Waalkes, Adam, Salipante, Stephen J.
Publicado 2019

Whole Genome Sequencing of Peruvian Klebsiella pneumoniae Identifies Novel Plasmid Vectors Bearing Carbapenem Resistance Gene NDM-1

por Roach, David, Waalkes, Adam, Abanto, Jorge, Zunt, Joseph, Cucho, Carolina, Soria, Jaime, Salipante, Stephen J
Publicado 2020

Identification of Leptotrichia goodfellowii infective endocarditis by next-generation sequencing of 16S rDNA amplicons

por Lieberman, Joshua A., Kurosawa, Kyoko, SenGupta, Dhruba, Cookson, Brad T., Salipante, Stephen J., Busch, David
Publicado 2021

In Silico Evaluation of Variant Calling Methods for Bacterial Whole-Genome Sequencing Assays

por Seah, Yee Mey, Stewart, Mary K., Hoogestraat, Daniel, Ryder, Molly, Cookson, Brad T., Salipante, Stephen J., Hoffman, Noah G.
Publicado 2023

Decoding cell lineage from acquired mutations using arbitrary deep sequencing

por Carlson, Cheryl A, Kas, Arnold, Kirkwood, Robert, Hays, Laura E, Preston, Bradley D, Salipante, Stephen J, Horwitz, Marshall S
Publicado 2011

Use of somatic mutations to quantify random contributions to mouse development

por Zhou, Wenyu, Tan, Yunbing, Anderson, Donovan J, Crist, Eva M, Ruohola-Baker, Hannele, Salipante, Stephen J, Horwitz, Marshall S
Publicado 2013

Characterization of the Mechanisms of Daptomycin Resistance among Gram-Positive Bacterial Pathogens by Multidimensional Lipidomics

por Hines, Kelly M., Waalkes, Adam, Penewit, Kelsi, Holmes, Elizabeth A., Salipante, Stephen J., Werth, Brian J., Xu, Libin
Publicado 2017

Evolution of cefiderocol resistance in Stenotrophomonas maltophilia using in vitro serial passage techniques

por Werth, Brian J., Ashford, Nathaniel K., Penewit, Kelsi, Waalkes, Adam, Holmes, Elizabeth A., Bryan, Andrew, Salipante, Stephen J.
Publicado 2022

CADD score has limited clinical validity for the identification of pathogenic variants in non-coding regions in a hereditary cancer panel

por Mather, Cheryl A, Mooney, Sean D, Salipante, Stephen J, Scroggins, Sheena, Wu, David, Pritchard, Colin C, Shirts, Brian H
Publicado 2016

Isolated MLH1 Loss by Immunohistochemistry Because of Benign Germline MLH1 Polymorphisms

por Bosch, Dustin E., Yeh, Matthew M., Salipante, Stephen J., Jacobson, Angela, Cohen, Stacey A., Konnick, Eric Q., Paulson, Vera A.
Publicado 2022