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1000 bootstrap replications  (STATA Corporation)


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    STATA Corporation 1000 bootstrap replications
    1000 Bootstrap Replications, supplied by STATA Corporation, used in various techniques. Bioz Stars score: 99/100, based on 49672 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/1000+bootstrap+replicates/STATA+14%2E0/pm36573295-80-12-9
    Average 99 stars, based on 49672 article reviews
    1000 bootstrap replications - by Bioz Stars, 2026-10
    99/100 stars

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    Article Snippet: Purpose: Functional recovery after robot-assisted radical prostatectomy (RARP) does not always align with patient-perceived bother.. To evaluate urinary/sexual bother-function relationships and time to acceptable bother using the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP).. Materials and Methods: We performed a retrospective cohort study of consecutive men undergoing RARP (April 2015−August 2025) who completed preoperative and ≥1 postoperative EPIC-CP assessment.

    Article Title: Bismuth-containing quadruple therapy for Helicobacter pylori infection in penicillin‑allergic children: efficacy, safety and real‑world experience from China.
    Article Snippet: 1 Department of Gastroenterology, Children’s Hospital of Fudan University, National Children’s Medical Center, 399 Wanyuan Road, Shanghai 201102, China 2 Department of Pediatrics, People’s Hospital of Lincang, 116 Nantang Street, Yunnan 677000, China Abstract Purpose To assess the efficacy and safety of 14-day bismuth-containing quadruple therapy (BQT) as both first-line and rescue treatment for children with Helicobacter pylori infections and penicillin allergies in China.. Methods This real-world, exploratory, retrospective observational cohort study enrolled children aged 6 to 18 years who underwent gastroendoscopy.. The eradication status was assessed at least 4 weeks after treatment completion.



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    Article Snippet: All analyses were performed using Stata version 14 (StataCorp, College Station, TX, USA).

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    Article Snippet: .. Statistical Analysis Evidence synthesis was conducted using Stata 14.0 (Stata Corp, College Station, TX, USA) and R (version 4.1.1). ..

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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