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Spss 17.0 statistical analysis software

Manufactured by IBM
Sourced in United States

SPSS 17.0 is a statistical analysis software package developed by IBM. It provides a comprehensive set of tools for data analysis, including descriptive statistics, advanced statistical modeling, and data visualization. The software is designed to help users analyze and interpret complex data, without making any claims about its intended use or application.

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Lab products found in correlation

13 protocols using spss 17.0 statistical analysis software

1

Genetic Analysis of Reproductive Traits

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The SPSS17.0 statistical analysis software (SPSS, Inc., Chicago, IL, USA) was used to calculate gene (haplotype) and genotype frequencies, as well as to perform a significance test of the difference between gene (haplotype) and genotype frequency (c 2 independence test), gene heterozygosity, and the effective number of alleles (Weaver and Wuensch, 2013) . The SHEsis analysis software was used to calculate the parameters of linkage disequilibrium (Shi and He, 2005) . In this test, the general linear model procedure of the SPSS17.0 statistical analysis software was used for correlation analysis between FSHR gene polymorphisms and TNB and NBA. The least significant difference method was used for multiple comparisons, and the corresponding TNB and NBA of different genotypes are reported as the least squares means ± standard error. The linear model was as follows:
where Y ijkl is the observed value of traits; µ is the overall mean; a i is the year and seasonal effect; b j is the genotype effect; c k is the effect of birth parity; d l is the breed effect; and e ijkl are random-residual effects.
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2

Measurement of Protein Concentration

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All results are expressed as the mean ± standard deviation of data obtained from triplicate experiments. All analyses were performed using SPSS 17.0 statistical analysis software (SPSS, Inc., Chicago, IL, USA). Two-tailed Student's t-test was used for all statistical analyses, with P<0.05 considered to indicate a statistically significant difference.
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3

Statistical Analysis Methodology for Biological Data

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Data are expressed as means ± SD. Data variance in data for animal and organ weight and haematological and serum biochemistries were assessed for homogeneity with Levene's procedure. If the variance was homogeneous, the data were assessed by one-way analysis of variance followed by the Dunnett post hoc test. If not, the Tamhane T2 test was applied. Differences at 95% confidence levels (p < 0.05) were considered significant. Statistical analyses were performed using SPSS 17.0 statistical analysis software (SPSS Inc., Chicago, IL).
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4

Statistical Analysis of Experimental Data

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All statistical analyses were performed using SPSS 17.0 statistical analysis software. Data are shown as the mean±SD in the text and figures. Comparisons between paired and unpaired groups were performed using the t-test or one-way ANOVA with Bonferroni correction < 0.05 considered to be statistically significant. The diagrams were prepared using Corbett real-time PCR, FACS, and SPSS software packages.
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5

Blinded Animal Experiment Analysis

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All data analysts were blind to animal experimental group members. Continuous variables were expressed as ±s, categorical data were expressed as M(means median). Statistical analysis was done using SPSS 17.0 statistical analysis software (SPSS). Normal distribution was achieved by log transformation for some skewed data. Comparison among the four groups was done using ANOVA or Rank Sum Test; multiple comparison was executed by Least Significant Difference - t test(LSD-t) or Student - Newman - Keuls(SNK).
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6

Statistical Analysis of Gastric Cancer

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The SPSS 17.0 statistical analysis software (Armonk, NY, USA) was used for the statistical analysis of the experimental data. The significance of differences between groups was estimated by Student's t-test and the χ2 test. The levels of HOTAIR in the gastric cancer patients were compared using the Mann-Whitney U test. The levels of HOTAIR, CDH1 and miR34a in the gastric cancer patients were assessed by the Spearman's correlation analysis. The disease-free survival probability was analyzed using Kaplan–Meier methods and evaluated using the log-rank test. A P-value <0.05 were considered significant.
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7

Comprehensive Analysis of Chemical Compounds

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All experiments were performed independently at least 3 times. Data are presented as mean ± standard deviation of three replicates. SPSS17.0 statistical analysis software (SPSS Inc.) was used to conduct normality test, variance homogeneity test, one-way ANOVA and repeated measures analysis of variance for the experimental data. For pairwise comparisons, Dunnett's T3 was used when the variances were unequal, and LSD was used when the variances were homogeneous.
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8

Microsatellite Loci Analysis for Parentage

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The average allele numbers, mean expected heterozygosity, and polymorphic information content (PIC) of the microsatellite loci were calculated using CERVUS version 3.0 (Kalinowski, Taper, & Marshall, 2007). The parentage analysis module available in CERVUS was used to calculate the success of assignment of candidate parents to the offspring. CERVUS uses a log (base e) likelihood algorithm to calculate the likelihood ratio (LOD) of a candidate male being the true parent compared with an random male. LOD scores are calculated for all possible sires, and the difference between the two most likely candidates (delta) is calculated and provides an indication of the reliability of the assignment. The delta score is calculated at a confidence level of 95% and corresponds to an estimated frequency of false positives of 5% (Moon, McCoy, Mushinsky, & Karl, 2006; Roques et al., 2004). First, the candidate mothers of each clutch were verified. Once the candidate mother and the offspring were matched, the paternal alleles were deduced from the comparison of both maternal and offspring genotypes. We assumed that clutches with more than two paternal alleles were multiple paternity. SPSS 17.0 Statistical Analysis Software and Pearson correlation coefficients were used to analyze correlations between variables (e.g., body size of female or male, clutch size, and the number of offspring).
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9

Statistical Analysis of Experimental Data

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SPSS 17.0 statistical analysis software (SPSS Inc., Chicago, IL, USA) was used for the data analysis. Measurement data are expressed as mean ± standard deviation. An independent-samples t test was used for normally distributed data, a rank sum test was used for non-normally distributed data, and an χ2 test was used for comparisons of count data. A P value of <0.05 indicated statistical significance.
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10

Statistical Analysis of Biological Samples

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Parametric test was used to compare samples in case of continuous variables, normal distribution and appropriate numerousness. The Shapiro–Wilk test was used to verify normal distribution. The Levene test was used to evaluate homogeneity of the variances. As parametric test, we used two-tailed Student t test to compare the average of the variables for homoscedastic paired groups. As nonparametric test, we used the two-tailed Wilcoxon signed-rank test for paired group. Continuity correction was applied in case of discrete distribution. P-values < 0.05 were considered significant. SPSS 17.0 statistical analysis software (SPSS Inc., Chicago, Illinois, USA) was used to perform statistical analysis.
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