Accurate, rapid and high-throughput detection of strain-specific polymorphisms in Bacillus anthracis and Yersinia pestis by next-generation sequencing
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* Corresponding author: Paul Keim paul.keim@nau.edu
1 Life Technologies Corporation, Foster City, California, USA
2 University of North Texas Health Science Center, Fort Worth, Texas, USA
3 Northern Arizona University, Flagstaff, Arizona, USA
4 Translational Genomics Research Institute, Phoenix, Arizona, USA
Investigative Genetics 2010, 1:5 doi:10.1186/2041-2223-1-5
Published: 1 September 2010Additional files
Additional file 1:
B. anthracis SNPs. A table in Microsoft Excel format of B. anthracis SNPs identified in this study by SOLiD™ system sequencing.
Format: XLS Size: 246KB Download file
This file can be viewed with: Microsoft Excel Viewer
Additional file 2:
Y. pestis SNPs. A table in Microsoft Excel format of Y. pestis SNPs identified in this study by SOLiD™ system sequencing.
Format: XLS Size: 46KB Download file
This file can be viewed with: Microsoft Excel Viewer
Additional file 3:
Y. pestis CO92 sequence corrections. A table in PDF format of corrections made to the Y. pestis CO92 reference chromosome sequence.
Format: PDF Size: 41KB Download file
This file can be viewed with: Adobe Acrobat Reader
Additional file 4:
TaqMan® oligonucleotide sequences. A table in PDF format of assay oligonucleotide sequences used for real-time PCR verification of putative genomic amplification regions.
Format: PDF Size: 40KB Download file
This file can be viewed with: Adobe Acrobat Reader
