Index of papers in April 2015 that mention

**p-value**

Analysis of CD data—gene analysis | The results of the gene analyses of the CD data are summarized in Table 2, which shows the number of significant genes at a number of different p-value thresholds. |

Analysis of CD data—gene-set analysis | The comparison of competitive methods is somewhat more complicated, due to the fact that ALIGATOR, INRICH and MAGENTA all use discretization using a p-value cutoff. |

Analysis of CD data—gene-set analysis | For INRICH the results are strongly dependent on the SNP p-value cutoff used, with three significant gene sets at the 0.0001 cutoff but none at the higher ones, further emphasizing the problem of choosing the correct cutoff. |

Analysis of CD data—gene-set analysis | This suggests that the different methods, or methods at different p-value cutoffs, are sensitive to distinctly different kinds of gene set associations. |

Analysis of summary SNP statistics | For the mean 12 statistic, a gene p-value is then obtained by using a known approximation of the sampling distribution [20,21]. |

Analysis of summary SNP statistics | For the top 12 statistic such an approximation is not available, and therefore an adaptive permutation procedure is used to obtain an empirical gene p-value . |

Analysis of summary SNP statistics | The empirical p-value for a gene is then computed as the proportion of permuted top 12 statistics for that gene that are higher than its observed top 12 statistic. |

Gene analysis | The gene analysis in MAGMA is based on a multiple linear principal components regression [18] model, using an F-test to compute the gene p-value . |

Gene-set analysis | To perform the gene-set analysis, for each gene g the gene p-value pg computed with the gene analysis is converted to a Z—value 2g 2 (ID—1(1 — pg), where (ID—‘1L is the probit function. |

p-value is mentioned in 17 sentences in this paper.

Topics mentioned in this paper:

- SNP (21)
- gene sets (20)
- regression model (20)

Biological validation analysis | First we identify the set of GO terms (pathways) that are significantly enriched within the given set of seed genes using Fisher’s exact test (Bonferroni corrected p-value <0.5). |

DIAMOnD implementation | (2) and consequently a lower p-value . |

DIAMOnD implementation | Similarly, between two proteins with the same number of connections to seeds k5, the one with lower k will result in lower p-value . |

DIAMOnD implementation | Finally, we calculate the exact p-value for the remaining nodes. |

Disease-gene associations | We use a genome-wide significance cutoff of p-value g 5 - 10—8. |

Interaction patterns of disease proteins within the Interactome | We found that only between ~ 1%-5% of the communities detected by the different methods are significantly enriched ( p-value < 0.05, Fisher’s exact test) with any set of disease proteins (Fig. |

Interaction patterns of disease proteins within the Interactome | To evaluate Whether a certain protein has more connections to seed proteins than expected under this null hypothesis, we calculate the connectivity p-value , i.e. |

Interaction patterns of disease proteins within the Interactome | 1H shows that the connectivity p-val-ues within the sets of known disease proteins are very significantly ( p-value < 10—241, Kolmogorov-Smirnov test) shifted towards smaller values when compared to the distributions expected for randomly scattered proteins. |

The DIAMOnD algorithm | lowest p-value ) is added to the set of seed nodes, increasing their number from so —>51 2 50+1. |

Validating disease modules | the number of seed genes 5 on which the p-value in Eqs. |

p-value is mentioned in 10 sentences in this paper.

Topics mentioned in this paper:

- p-value (10)
- true positives (9)
- connected component (4)

Data | If the null hypothesis of statistical independence of these two variables cannot be rejected in a chi-squared test using a p-value of p = 0.05 the seX ratio is set to zero, SR(x,t) = O. Lead/lag indicator. |

Data | The p-value for each lead and lag indicator is the probability of obtaining the observed values for I lead(d,-,x) and I lag(d,-,x) from the surrogate data. |

Further comorbidities | In the enlarged sample only one out of the 123 comorbidities using the inpatient sample has a p-value greater than 0.05 (M23), all other remain significant (p<0.05). |

Results/Discussion | Lead/lag behavior is identified for male and female DM1 and DMZ patients if the null hypothesis that the observed indicator values for I lead(di,x) and I lag(d,-,x) can be obtained from randomized surrogate data can be rejected with a p-value of p< 0.01. |

Supporting Information | For the age groups with the smallest p-value the relative risks RR, patient ages, and the corresponding p-values are shown for DM1 and DM2, respectively. |

Supporting Information | Comorbidity data for DMl patients, the relative risks RRI, the confidence intervals for RRI, if applicable the p-Value for the co-occurrence analysis, and the sex ratio for each diagnosis and age group. |

Supporting Information | Comorbidity data for DM2 patients, the relative risks RRZ, the confidence intervals for RRZ, if applicable the p-Value for the co-occurrence analysis, and the sex ratio for each diagnosis and age group. |

p-value is mentioned in 7 sentences in this paper.

Topics mentioned in this paper:

- age group (10)
- p-value (7)
- discovery rate (5)

Enrichment of particular logic gates among consistent triplets by hyper-geometric test | Given a set of triplets (e.g., the triplets in Which RFl is MYC) and a particular logic gate g, we calculate a hyper-geometric enrichment p-Value to describe the enrichment of triplets consistent With the gate g as opposed to other gates as follows: The p-Value is equal kg is the number of triplets consistent With the gate g in the set, K is the total number of triplets consistent With the gate g, and N is the total number of triplets. |

Loregic applications for other regulatory features | Out of these, 162 are consistent with the AND gate (with enrichment by hypergeometric test p-value <1.3*10'3), and 159 are consistent with “T 2 RH” (with enrichment by hypergeometric test p-value <7.5*10'5) making them the dominant logic gates for yeast FFL. |

Loregic applications for other regulatory features | From these triplets, 446 match “T = RFZ” When RF2 is MYC (hy-pergeometric test p-value < 2.5*10'124), and 201 match “T = ~RF1+RF2” When RF1 is a miRNA and RF2 is MYC (hypergeometric test p-value < 4.1*10'25). |

Validation | For example, in analyzing 871 AND-gate-consistent triplets, we found that deleting either of their TFs gave rise to substantial down-regulation of their target genes, i.e., the logarithm expression fold changes were significantly less than zero (t-test p-value = 0.068). |

Validation | The two most enriched logic gates are “T = RF1” (133 triplets, hypergeometric test p-value < 4.3*10' 27) and “T = RF1+RF2 (OR)” (211 triplets, hypergeometric test p-value < 1.1*10'21) |

p-value is mentioned in 5 sentences in this paper.

Topics mentioned in this paper:

- gene expression (39)
- regulatory network (17)
- expression data (12)

Insights into the functions of ORFs with peak in 3’UTR | with lowest p-value ) are identified for a range of 31 to 86 ORFs per GO term, with a mean value of 62.3 ORFs per GO term. |

Statistical analysis | All enrichment Widgets list a term, a count and an associated p-Value . |

Statistical analysis | The p-Value is the probability that result occurs by chance, thus a lower p-Value indicates greater enrichment Without corrections. |

Statistical analysis | The p-Value is calculated using the Hypergeometric distribution. |

p-value is mentioned in 4 sentences in this paper.

Topics mentioned in this paper:

- mRNA (16)
- gene expression (9)
- transcriptional (8)

PEACS: Algorithm | To calculate a p-Value , a Monte Carlo sampling algorithm was implemented. |

PEACS: Algorithm | The p-Value was defined as the rank of the real PEACS score in the null distribution diVided by 10,000. |

Results | The empirical p-value was then determined by ranking the PEACS score for the given perturbation relative to the PEACS scores generated by this Monte Carlo procedure. |

Supporting Information | Displayed are the PEACS scores, uncorrected p-Value, Bonferroni corrected p-Value , and significance (* = raw p<0.01; T = Bonfer-roni-corrected p<0.05) for genes with at least 3 knockdown conditions with 2-fold or higher knockdown. |

p-value is mentioned in 4 sentences in this paper.

Topics mentioned in this paper:

- stem cells (40)
- ICA (10)
- gene expression (7)

Pairwise covariation | Kendall's tau-b for each such pair is calculated with an accompanying Z-score from which a p-value can be calculated. |

Supporting Information | PR-PR pairs ranked by Fisher exact test p-Value calculated from 2013 HIVDB sequences. |

The pooled proportion PP _PS ><N5+Pf ><Nf | From these quantities, a Z-score and p-Value can be computed assuming a normal distribution using Z = (PfPs)/SE. |

The pooled proportion PP _PS ><N5+Pf ><Nf | A p-Value is computed for each mutation at all 599 positions for Which the mutation is detectable in at least 5 patients Who failed therapy. |

p-value is mentioned in 4 sentences in this paper.

Topics mentioned in this paper:

- mutual information (18)
- sequencing data (17)
- amino acid (15)

Supervised learning: Classification | The coefficients give the relative importance of each feature to the predictor; associated p-values indicate the confidence in those coefficient values (a large p-value indicates an unreliable estimate of the feature contribution). |

Unsupervised learning | Antibody feature:function and feature:feature correlations were computed over the set of 80 vaccinated subjects and assessed using Pearson correlation coefficient and p-value . |

Unsupervised learning | For each function and each group, the feature with the largest-magnitude feature:function correlation coefficient was identified; each such feature also had the best feature:function p-value within its group, < = 0.001. |

p-value is mentioned in 3 sentences in this paper.

Topics mentioned in this paper:

- cytokine (16)
- principal components (16)
- machine learning (13)