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exact wilcoxon rank sum tests  (SAS institute)


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    SAS institute exact wilcoxon rank sum tests
    (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using <t>exact</t> <t>Wilcoxon</t> <t>rank</t> <t>sum</t> <t>tests</t> using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).
    Exact Wilcoxon Rank Sum Tests, supplied by SAS institute, 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/exact+wilcoxon+rank-sum+test/pmc10402036-228-0-19?v=SAS+institute
    Average 90 stars, based on 1 article reviews
    exact wilcoxon rank sum tests - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Non-neutralizing SARS-CoV-2 N-terminal domain antibodies protect mice against severe disease using Fc-mediated effector functions"

    Article Title: Non-neutralizing SARS-CoV-2 N-terminal domain antibodies protect mice against severe disease using Fc-mediated effector functions

    Journal: bioRxiv

    doi: 10.1101/2023.07.25.550460

    (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using exact Wilcoxon rank sum tests using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).
    Figure Legend Snippet: (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using exact Wilcoxon rank sum tests using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).

    Techniques Used: Virus, Infection, Control



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    (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using <t>exact</t> <t>Wilcoxon</t> <t>rank</t> <t>sum</t> <t>tests</t> using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).
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    (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using exact Wilcoxon rank sum tests using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).

    Journal: bioRxiv

    Article Title: Non-neutralizing SARS-CoV-2 N-terminal domain antibodies protect mice against severe disease using Fc-mediated effector functions

    doi: 10.1101/2023.07.25.550460

    Figure Lengend Snippet: (A) Study design. BALB/c mice were passively infused at −12 hours and challenged with SARS-CoV-2 MA10 virus at 0 hours. Weights for each animal were collected each day of the experiment and lung tissue was harvested four days post-infection (DPI) to measure infectious viral titers and assign the gross lung discoloration (GLD) score. N = 10 mice per test group; n = 25 isotype control mice; n = 5 uninfected mice. (B) Percent weight loss in mice administered DH1052 G1m17, DH1050.1 G1m17, or Isotype control antibody. Uninfected mice were included as negative controls for weight loss. (C-E) Non-nAb DH1052 and (F-H) nAb DH1050.1 protection against infection and disease. Protection was assessed by (C,F) lung viral titers quantified as the log(PFU/mL), (D,G) weight loss each day post-infection (DPI) expressed as % original weight, and (E,H) median gross lung discoloration scores. All statistical comparisons were calculated using exact Wilcoxon rank sum tests using an alpha level of 0.05 (* p<0.05; ** p<0.01; *** p<0.001).

    Article Snippet: Exact Wilcoxon rank sum tests were performed using an alpha level of 0.05 to compare differences between groups using SAS (SAS Institute, Cary, NC).

    Techniques: Virus, Infection, Control