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Volume 31, Supplement—May 2025

SUPPLEMENT ISSUE
Supplement

Integrating Genomic Data into Public Health Surveillance for Multidrug-Resistant Organisms, Washington, USA

Laura Marcela Torres1Comments to Author , Jared Johnson1, Audrey Valentine1, Audrey Brezak, Emily C. Schneider, Marisa D’Angeli, Jennifer Morgan, Claire Brostrom-Smith, Chi N. Hua, Michael Tran, Darren Lucas, Joenice Gonzalez De Leon, Drew MacKellar, Philip Dykema, Kelly J. Kauber, and Allison Black
Author affiliation: Washington State Department of Health, Shoreline, Washington, USA (L.M. Torres, J. Johnson, A. Valentine, A. Brezak, E.C. Schneider, M. D’Angeli, C.N. Hua, M. Tran, D. Lucas, J. Gonzalez De Leon, D. Mackellar, P. Dykema, K.J. Kauber, A. Black); Public Health Seattle and King County, Seattle, Washington, USA (J. Morgan, C. Brostrom-Smith)

Main Article

Figure 3

SNP matrix showing number of polymorphic sites observed when making pairwise comparisons between the core genome of the sequences in a cluster of Klebsiella pneumoniae carbapenemase–producing K. pneumoniae isolates as part of study of integrating genomic data into public health surveillance for multidrug-resistant organisms, Washington, USA. Dark gray represents lower SNP distances and light gray larger SNP distances. Diff, difference; PT, patient; ref., reference; SNP, single-nucleotide polymorphism.

Figure 3. SNP matrix showing number of polymorphic sites observed when making pairwise comparisons between the core genome of the sequences in a cluster of Klebsiella pneumoniae carbapenemase–producing K. pneumoniae isolates as part of study of integrating genomic data into public health surveillance for multidrug-resistant organisms, Washington, USA. Dark gray represents lower SNP distances and light gray larger SNP distances. Diff, difference; PT, patient; ref., reference; SNP, single-nucleotide polymorphism.

Main Article

1These first authors contributed equally to this article.

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