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Applied Maths bionumerics software program
Bionumerics Software Program, supplied by Applied Maths, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bionumerics+program/bionumerics+software/10__1016_slash_j__fm__2025__104762-66-6-11
Average 90 stars, based on 1 article reviews
bionumerics software program - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

other:

Article Title: Brucellosis re-emergence after a decade of quiescence in Palestine, 2015-2017: A seroprevalence and molecular characterization study.
Article Snippet: We would like to thank the Applied Maths team for their help and time during data analysis using the BioNumerics program.

Denaturing Gradient Gel Electrophoresis:

Article Title: Environmental Risk Assessment of Living Modified Microorganisms (LMM) on the Indigenous Microbial Community
Article Snippet: .. DGGE profile of the microcosm experiment was then subjected to Pearson correlation cluster analysis using the BioNumerics program (Applied Maths, Belgium) and other statistical analysis was performed by XLSTAT software (Addinsoft, France) [13]. ..

Software:

Article Title: Environmental Risk Assessment of Living Modified Microorganisms (LMM) on the Indigenous Microbial Community
Article Snippet: .. DGGE profile of the microcosm experiment was then subjected to Pearson correlation cluster analysis using the BioNumerics program (Applied Maths, Belgium) and other statistical analysis was performed by XLSTAT software (Addinsoft, France) [13]. ..

Article Title: Lebanon’s Native Oenological Saccharomyces cerevisiae Flora: Assessment of Different Aspects of Genetic Diversity and Evaluation of Winemaking Potential
Article Snippet: .. Gel pictures were normalized using the Bionumerics program (Applied Maths, version 1.01) and the profiles were clustered using the neighbour-joining aggregation method based on Dice coefficient from the same software. ..

Construct:

Article Title: Antibiotics Combinations and Chitosan Nanoparticles for Combating Multidrug Resistance Acinetobacter baumannii
Article Snippet: .. Analysis of ERIC-PCR dendrogram was constructed using the UPGMA clustering method, Bionumerics program version 7.6 (Applied Maths). ..

Sequencing:

Article Title: Frequency of first and second-line drug resistance-associated mutations among resistant Mycobacterium tuberculosis clinical isolates from São Paulo, Brazil
Article Snippet: .. To generate single consensus sequences, the nucleotide sequences were edited using the BioNumerics program version 7.6.3 (Applied Maths, Sint-Martens-Latem, Belgium), which were then compared with the M. tuberculosis H37Rv sequence deposited in the National Center for Biotechnology Information (NCBI) database under access number NC000962.3 (URL: http://www.ncbi.nlm.nih.gov/BLAST). .. Phenotypic and molecular drug susceptibility testing - Isolates with discrepancies between the phenotypic and sequencing results were retested for drug susceptibility to first- (INH and RIF) and second-line drugs (LFX, AMK and KAN) as previously described., The identification of mutations that confer resistance to first- and second-line drugs was performed using line probe assays (LPA) GenoTypeMTBDR plus v2.0 and MTBDR sl v2.0 (HainLifescience, Nehren, Germany) with DNA from the isolates that was extracted from drug- and non-drug-containing MGIT tubes, and was performed according to instructions of the manufacturer.

Amplification:

Article Title: The diverse virulence potential of atypical enteropathogenic Escherichia coli isolated from diarrhea: the emergence of a hybrid pathotype?
Article Snippet: .. To determine a clonal relationship, the amplification pattern obtained for both primers was evaluated by the BioNumerics program version 7.6.3 (Applied Maths, Sint-Martens-Latem, Belgium). ..



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Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the <t>BioNumerics</t> and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.
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Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the <t>BioNumerics</t> and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.
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Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the <t>BioNumerics</t> and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.
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Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the <t>BioNumerics</t> and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.
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Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the BioNumerics and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.

Journal: Frontiers in Microbiology

Article Title: The diverse virulence potential of atypical enteropathogenic Escherichia coli isolated from diarrhea: the emergence of a hybrid pathotype?

doi: 10.3389/fmicb.2025.1599350

Figure Lengend Snippet: Dendrogram of six aEPEC presenting hybrid genotypes. Amplification profiles obtained in RAPD-PCR using primer 1247 (A) and primer 1283 (B) were evaluated by the BioNumerics and used to build the dendrogram. Note the proximity among strains 0811–4, 2071–1, 1482–11, and 2332–7. Strains 1551–3 and 3712–3 were less correlated. The red dashed line represents the cutoff of 90% similarity in the amplification pattern used to determine the clonality of the strains.

Article Snippet: To determine a clonal relationship, the amplification pattern obtained for both primers was evaluated by the BioNumerics program version 7.6.3 (Applied Maths, Sint-Martens-Latem, Belgium).

Techniques: Amplification