The largest database of trusted experimental protocols

Prism 8

Manufactured by Posit

Prism 8 is a versatile and precise lab equipment designed for optical analysis. It features a high-quality prism that can be used for tasks such as wavelength separation, refractive index measurement, and dispersion analysis. The device is built to deliver accurate and reliable results, making it a valuable tool for researchers and scientists working in various fields.

Automatically generated - may contain errors

20 protocols using prism 8

1

Statistical Analysis of Quantitative Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
All statistical analyses were performed in GraphPad Prism 8.0 and R studio 3.6.0. Quantitative data are represented with means ± standard deviation. Analysis of variance and Student's t-test were used to explore the differences among groups. P-values < 0.05 were considered statistically significant.
+ Open protocol
+ Expand
2

Survival Analysis of Cancer Patients

Check if the same lab product or an alternative is used in the 5 most similar protocols
Numerical data are expressed as the mean ± SEM (Standard Error Mean). Student's t-tests, ANOVAs and Chi-square tests were used for the evaluation of statistical significance, calculated with GraphPad Prism 8.0 or R Studio. P-values lower than 0.05 were considered significant with *p < 0.05, **p < 0.005, ***p < 0.001, and ****p < 0.0001. Progression free survival (PFS) was calculated from the date of study enrolment to the date of tumor progression. Kaplan-Meier survival curves were generated using R Studio® software (median with 95% confidence interval).
+ Open protocol
+ Expand
3

Statistical Analysis of Biological Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
Statistical analysis was performed on either GraphPad Prism 8.0 or RStudio. Plots were generated in R, mainly using the packages ggplot2, ggsci, ggrepel, and scales. For data sets with n>4, Box plots (Tukey style) were used. For data sets with n<5, average±s.d., including individual data points, is shown. Normal distribution of data was tested with the Shapiro-Wilk test. Based on the results, parametric (e.g., Student’s t-test) or nonparametric (e.g. Mann-Whitney and Kolmogorov-Smirnov) tests were used.
The detailed parameters (n, p value, test) for the statistical assessment of the data are provided in the figure legends.
+ Open protocol
+ Expand
4

Predicting Breast Cancer Drainage Tube Retention

Check if the same lab product or an alternative is used in the 5 most similar protocols
All statistical analyses were conducted using GraphPad Prism 8.0 software and RStudio software version 3.6.0. The enumeration data were used the Chi-square test, and the measurement data were used the t-test analysis. The univariate and multivariate logistic regression models were performed to access the risk factors for affecting drainage tube retention time in patients with breast cancer. The nomogram was validated predicting the risk for drainage tube retention time. Two-sided P values less than 0.05 were considered statistically significant.
+ Open protocol
+ Expand
5

Statistical Analysis of Recurrent UTI

Check if the same lab product or an alternative is used in the 5 most similar protocols
Statistical analyses were performed with GraphPad Prism 8.1.0 and RStudio version 4.0.2. Two-sided parametric (t and χ2) and nonparametric (Mann–Whitney) tests were used at α = 0.05 to test for group differences. The Z-score was calculated through Prism using the formula z=xμσ where x is the raw score, μ is the population mean, and σ is the SD. Logistic regression was used to determine the relationship between rUTI and cytokine concentration with a standard cutoff probability of 0.5. McFadden’s pseudo-R2 and its P-value were used to assess model fit. Leave-one-out cross-validation was used to evaluate the predictive power of each logistic model via AUC, sensitivity, specificity, misclassification rate, and F1-score. Receiver operating characteristic curves were generated by plotting the false-positive rate (1-specificity) against the true-positive rate (sensitivity).
+ Open protocol
+ Expand
6

Predicting Recurrent Urinary Tract Infections

Check if the same lab product or an alternative is used in the 5 most similar protocols
All statistical analyses were performed in GraphPad Prism 8.1.0 and R Studio version 4.0.2 with an α of 0.05. Hypothesis testing was performed using classical methods. Pairwise associations between continuous variables were performed using Spearman’s rho correlation with P-values generated by permutation. Differences between continuous variables by group were analyzed using ANOVA or t test if normally distributed, or the Mann–Whitney U test, Wilcoxon matched pairs signed rank test, or Kruskal–Wallis test with multiple comparison post hoc if not normally distributed. Differences between continuous variable by group were analyzed using ANOVA, t test, or Kruskal–Wallis test with multiple comparison post hoc. Differences between categorical variables were analyzed using chi-square, Fisher’s exact test, or ordinal logistic regression. Various logistic regression models were constructed to predict rUTI using combinations of all significant covariates. Model fit was assessed using McFadden’s pseudo-R2. The predictive power of each logistic regression model was assessed using F-scores and AUC attained through leave-one-out cross validation. Models were further compared using ANOVA.
+ Open protocol
+ Expand
7

Statistical Analysis of Experimental Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
All statistical analyses were performed by two-tailed Student’s t-test or Wilcoxon rank-sum test using GraphPad Prism8 and RStudio. All data were expressed as means ± s.d.
+ Open protocol
+ Expand
8

Statistical Analysis of Experimental Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
The statistical analysis and mapping were performed using Prism8 and Rstudio based on R version 4.0.4. A comparison between the two groups was performed using the two-tailed Student’s t-test. Data were expressed as means ± SEM, and a p-value < 0.05 was considered significant.
+ Open protocol
+ Expand
9

Comprehensive Statistical Analysis of Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
Data is shown as mean ± SD unless otherwise stated. GraphPad Prism 8 and RStudio software were used to examine the data for statistical significance between groups. ANOVA was used to assess the presence of statistically significant differences between the means of three or more independent groups, in all cases data followed a normal distribution. Post-hoc Bonferroni correction was performed for multiple group comparisons. Otherwise, Student’s t-test was used when data followed a normal distribution, alternatively Mann-Whitney test on ranks was used. Experiments were conducted at a minimum of triplicates and repeated 3–4 times. A p-value of < 0.05 was considered statistically significant.
+ Open protocol
+ Expand
10

Multiomic Analysis of Cell Phenotypes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Data from all phenotypic described above were first organized in a Microsoft Excel spreadsheet and analyzed using GraphPad PRISM 8 software or Rstudio. For MEA, qPCR data analysis and imaging analysis, values are expressed as mean ± s.e.m. All boxplots and violin plots represent the median and quartiles of the data. Statistical significance was tested using either two-sided Student’s t test, one-way ANOVA with Dunnett’s post-hoc test or two-way ANOVA with Holm-Sidak’s test as noted in the figure legends. Whole transcriptome RNA-seq analysis was performed in R using DeSeq2 and single-cell sequencing analysis was performed in R using Seurat. More information can be found in the Life Sciences Reporting Summary.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!