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bootstrap mediated effect tests  (STATA Corporation)


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    STATA Corporation bootstrap mediated effect tests
    Bootstrap Mediated Effect Tests, supplied by STATA Corporation, used in various techniques. Bioz Stars score: 99/100, based on 35135 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bootstrap/STATA+16%2E0/pmc12891216-86-3-8
    Average 99 stars, based on 35135 article reviews
    bootstrap mediated effect tests - by Bioz Stars, 2026-09
    99/100 stars

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    Article Title: Rural-Urban Differences in the Association Between Reproductive Coercion and Postpartum Family Planning.
    Article Snippet: All analyses were conducted using Stata version 16.1 (StataCorp 2019).

    Article Title: Socioeconomic and regional determinants of optimal antenatal care utilization among women in South and Central Somalia
    Article Snippet: The SDHS 2020 data were analyzed using STATA 16.

    Article Title: First dual-frame telephone survey for non-communicable disease risk and protective factors: Methods and main findings from a central Brazilian state, 2022
    Article Snippet: All analyses considered a 5 % significance level and were conducted using the survey module for complex samples in Stata version 16.0.

    Article Title: Drug resistance pulmonary tuberculosis among prisoners in Ethiopia: A systematic review and meta -analysis
    Article Snippet: Stata version 16 (Stata Corp LP, College Station, TX) was used for analysis.

    Software:

    Article Title: Drug resistance pulmonary tuberculosis among prisoners in Ethiopia: A systematic review and meta -analysis
    Article Snippet: .. Meta-analysis was computed using STATA version 16 software. ..

    Article Title: Hepatitis B virus testing, vaccination, and hepatitis B surface antigen prevalence among adult inpatients at an urban polyclinic in Accra, Ghana: a cross-sectional study
    Article Snippet: .. The data were analysed using STATA version 16.0 (Stata Statistical Software: Release 16; StataCorp LLC, College Station, Texas, USA). ..



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    Biomatters Ltd 1000 bootstrap replicates
    Phylogenetic analysis of Hepacivirus bovis (BovHepV). The complete BovHepV genome sequences were aligned using MAFFT. Subsequently, a maximum likelihood analysis was performed using the maximum likelihood method and <t>the</t> <t>Tamura–Nei</t> model, including <t>1000</t> bootstrap replicates (Geneious v.11.1.5 software package (Biomatters, New Zealand)). The scale indicates the nucleotide substitutions per site. The BovHepV strains analyzed in this study are marked with a black square. The viruses are labeled with their accession number, virus ID, and country of origin. The genome of the hepatitis GB virus was used as an outgroup. The corresponding genotypes and subtypes were defined on the basis of a previous publication .
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    Phylogenetic analysis of Hepacivirus bovis (BovHepV). The complete BovHepV genome sequences were aligned using MAFFT. Subsequently, a maximum likelihood analysis was performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates (Geneious v.11.1.5 software package (Biomatters, New Zealand)). The scale indicates the nucleotide substitutions per site. The BovHepV strains analyzed in this study are marked with a black square. The viruses are labeled with their accession number, virus ID, and country of origin. The genome of the hepatitis GB virus was used as an outgroup. The corresponding genotypes and subtypes were defined on the basis of a previous publication .

    Journal: Viruses

    Article Title: Identification and Long-Term Detection of Hepacivirus bovis Genotype 1 and 2 on a Cattle Farm in Germany

    doi: 10.3390/v18010078

    Figure Lengend Snippet: Phylogenetic analysis of Hepacivirus bovis (BovHepV). The complete BovHepV genome sequences were aligned using MAFFT. Subsequently, a maximum likelihood analysis was performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates (Geneious v.11.1.5 software package (Biomatters, New Zealand)). The scale indicates the nucleotide substitutions per site. The BovHepV strains analyzed in this study are marked with a black square. The viruses are labeled with their accession number, virus ID, and country of origin. The genome of the hepatitis GB virus was used as an outgroup. The corresponding genotypes and subtypes were defined on the basis of a previous publication .

    Article Snippet: A maximum likelihood analysis was subsequently performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates (Geneious v.11.1.5 software package (Biomatters, New Zealand)).

    Techniques: Software, Labeling, Virus

    Phylogenetic analysis of 55 partial BovHepV-1 sequences of the NS3 gene from the years 2020–2022. The partial BovHepV genome sequences were aligned using MAFFT. Subsequently, a maximum likelihood analysis was performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates. The scale indicates the nucleotide substitutions per site. The viruses are labeled with their accession number, cattle ID, sampling date, and sample ID. The table on the right summarizes several key observations: (I) different cattle carry genetically identical virus, (II) identical viruses persist for months or years in the same animal, (III) reinfections with novel BovHepV variants, either with alternative subtypes or genetically distinct strains within the same subtype, are possible. The letter–number combination continuously identifies the corresponding animals/samples in a subgroup. Examples of how to interpret the table in the figure are as follows: Column I: The four cattle in subgroup A (A1, A2, A3, and A4) all carry a virus with the identical NS3 gene sequence. Column II: In cattle R885, the identical virus sequence was found in four samples taken between October 2020 and 22 October (M1 to M4 in column II). The accession numbers and sample IDs are also summarized in .

    Journal: Viruses

    Article Title: Identification and Long-Term Detection of Hepacivirus bovis Genotype 1 and 2 on a Cattle Farm in Germany

    doi: 10.3390/v18010078

    Figure Lengend Snippet: Phylogenetic analysis of 55 partial BovHepV-1 sequences of the NS3 gene from the years 2020–2022. The partial BovHepV genome sequences were aligned using MAFFT. Subsequently, a maximum likelihood analysis was performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates. The scale indicates the nucleotide substitutions per site. The viruses are labeled with their accession number, cattle ID, sampling date, and sample ID. The table on the right summarizes several key observations: (I) different cattle carry genetically identical virus, (II) identical viruses persist for months or years in the same animal, (III) reinfections with novel BovHepV variants, either with alternative subtypes or genetically distinct strains within the same subtype, are possible. The letter–number combination continuously identifies the corresponding animals/samples in a subgroup. Examples of how to interpret the table in the figure are as follows: Column I: The four cattle in subgroup A (A1, A2, A3, and A4) all carry a virus with the identical NS3 gene sequence. Column II: In cattle R885, the identical virus sequence was found in four samples taken between October 2020 and 22 October (M1 to M4 in column II). The accession numbers and sample IDs are also summarized in .

    Article Snippet: A maximum likelihood analysis was subsequently performed using the maximum likelihood method and the Tamura–Nei model, including 1000 bootstrap replicates (Geneious v.11.1.5 software package (Biomatters, New Zealand)).

    Techniques: Labeling, Sampling, Virus, Sequencing