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Transcripts that showed significantly decreased expression in tetraploid N2 comparing to diploid N2 animals at L4 larva stage. |
DESeq2 R package (1.20.0), fold change > 2, and FDR < 0.05. |
WBPaper00066110:tetraploid_vs_diploid_downregulated
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Transcripts that showed significantly decreased expression in hda-2(ok1479) comparing to in N2 animals. |
DESeq2 (version 1.28.1), FDR < 0.01, fold change > 2. |
WBPaper00062159:hda-2(ok1479)_downregulated
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Top 300 transcripts enriched in MC neuron, MCL, MCR according to single cell RNAseq. |
Top 300 enriched transcripts were determined by log2.ratio of the tpm in the cell type vs the tpm in the other cells * the log2 of the cell.type tpm. |
WBPaper00061340:MC
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Temperature Shift: 25C vs 15C for 16 hours at L4 larva stage. |
Transcripts that showed significantly increased expression in AFD neurons at lin-15(n765ts); oyIs95 animals shifted from 20C to 25C for 16 hours at L4 larva stage, comparing to animals shifted from 20C to 15C for 16 hours at L4 larva stage. |
DESeq2, fold change > 2, FDR < 0.05. |
WBPaper00065158:25C_vs_15C_upregulated_AFD
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Transcripts that showed significantly decreased expression after 24 hours of induction of human beta Amyloid at young adult stage |
A 2-fold change in expression level and a false discovery rate analog of p < 0.05. |
WBPaper00064130:Beta-Amyloid_24h_downregulated_mRNA
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Transcripts that showed significantly decreased expression in diploid N2 animals after exposure to 5uM cisplatin for 72 hours at 15C from L1 to L4 larve stage. |
DESeq2 R package (1.20.0), fold change > 2, and FDR < 0.05. |
WBPaper00066110:Cisplatin_downregulated_diploid
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Transcripts that showed significantly decreased expression in diploid N2 animals after exposure to 5 uM doxorubicin for 72 hours at 15C from L1 to L4 larve stage. |
DESeq2 R package (1.20.0), fold change > 2, and FDR < 0.05. |
WBPaper00066110:Doxorubicin_downregulated_diploid
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Transcripts that showed significantly decreased expression in hsf-1(RNAi) comparing to in ash-2 animals injected with vector. |
Differential mRNA expression using DESeq2. mRNAs with a FDR < 0.05 and fold change > 2 considered differentially expressed. |
WBPaper00066232:hsf-1(RNAi)_downregulated_ash-2
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Transcripts the showed altered expression after auxin induced sacy-1 depletion (24 hours of 2mM auxin treatment at 20C starting from young adult hermaphrodite stage). |
DESeq2 |
WBPaper00059334:sacy-1(depletion)_regulated
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Transcripts that showed significantly decreased expression in him-17(me24) comparing to in N2 animals. |
DESeq2, fold change > 2, FDR < 0.05. |
WBPaper00064769:him-17(me24)_downregulated
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fasting |
Genes upregulated by fasting anytime during the 48 hour time course in N2 worms. |
Hierarchical clustering analysis was done with squared Euclidean as the distance metric and average linkage as the cluster method by using GeneSpring GX. |
WBPaper00041960:N2_fasting_upregulated_anytime
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Transcripts that showed significantly increased expression in mir- 229,64,65,66(nDf63) III comparing to in N2 animals. |
DESeq2 v1.30.1, fold change > 2, FDR < 0.05. |
WBPaper00064999:miR-229-64-65-66_upregulated
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Transcripts that showed significantly increased expression in DA116[eat-2(ad1116)] comparing to in N2. |
The DESeq2 package (v1.24.0) was used to identify differentially expressed genes (DEGs). Fold change > 2, FDR < 0.05. |
WBPaper00061040:eat-2(ad1116)_upregulated
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Transcripts that showed significantly increased expression in let-418(n3536) comparing to in N2. |
DESeq2, fold change > 2, p-value < 0.01. |
WBPaper00061203:let-418(n3536)_upregulated
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Top 300 transcripts enriched in ABplpppppp, ABprpppppp according to single cell RNAseq. |
Top 300 enriched transcripts were determined by log2.ratio of the tpm in the cell type vs the tpm in the other cells * the log2 of the cell.type tpm. |
WBPaper00061340:Parent_of_tail_spike_and_hyp10
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Expression Pattern Group F, enriched for genes involved in embryonic development. These patterns have in common that they all have genes of which the expression goes up after the juvenile stage. The expression of the genes in these patterns remains high or even goes up after reproduction. |
The significance (P 0.0001) of the relative age (time) was used to determine if a gene was differentially expressed between the three age (time) groups. The effect of this factor explaining gene expression differences was used to determine if the expression went up or down during the two age/time periods (t1 - t2 and t2 -t3). Authors used a permutation approach to determine the thresholds for the different mapping strategies. For each of the used models for eQTL mapping, authors used 23,000 permutations. For each permutation, authors randomly picked a spot; each spot could only be picked once. The gene expression and relative lifespan values were than randomly distributed over the RILs (and time points) and used for mapping. In this way, authors obtained a threshold for each of the explaining factors. For the single time points, authors used a FDR of 0.01 to adjust for multiple testing. The genome-wide threshold for this FDR is -log10 P = 3.8 for each of the three time points. For the combined models (t1 to t2 and t2 to t3), authors used a genome-wide threshold of -log10 P = 4, which resembles an FDR of 0.006, 0.001, and 0.006 for marker, age, and the interaction between marker and age, respectively. To determine the threshold for the single gene examples, authors used 1000 permutations as in the genome-wide threshold. The difference is that they use the gene under study in all of the permutations. The P-values for the gene specific thresholds were determined at FDR = 0.05. |
WBPaper00036286:Pattern_F
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Genes predicted to be upregulated more than 2.0 fold in rrf-2(ok210) mutant worms as compared to wild-type animals (t-test P-value < 0.05). |
A t-test (5% confidence) was applied to the triplicate sample data for each transcript in each mutant to identify genes significantly elevated or decreased compared with the wild type. |
WBPaper00027111:rrf-2(ok210)_upregulated
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Top 300 transcripts enriched in body wall muscle cell according to single cell RNAseq. |
Top 300 enriched transcripts were determined by log2.ratio of the tpm in the cell type vs the tpm in the other cells * the log2 of the cell.type tpm. |
WBPaper00061340:Body_wall_muscle
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Genes that showed significantly increased experssion after 22.5 hours of treatment in 200nM delta7-dafachronic acid comparing with in ethanol vehicle control. |
To identify the differentially expressed genes, we applied Significance Analysis of Microarrays (SAM) analysis using the R package samr [46]. Genes with median false discovery <5% and fold changes >2.0 were considered differentially expressed. |
WBPaper00046548:dafachronic-acid_upregulated
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Heat Shock: 5 min at 34C. |
Transcripts that showed significantly decreased expression after 5 minutes heat shock at 34C. |
DESeq2,, FDR < 0.01 |
WBPaper00059598:HeatShock_downregulated
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Up-Regulated genes under 0.5mg/l CPF+ 1 mg/l DZN treatment at 16 centigrade. |
The Rank Product package was used to identify the differentially expressed genes between controls and treatment in each experiment. Briefly, genes were ranked based on up- or downregulation by the treatment in each experiment. Then, for each gene a combined probability was calculated as a rank product (RP). The RP values were used to rank the genes based on how likely it was to observe them by chance at that particular position on the list of differentially expressed genes. The RP can be interpreted as a p-value. To determine significance levels, the RP method uses a permutation-based estimation procedure to transform the p-value into an e-value that addresses the multiple testing problem derived from testing many genes simultaneously. Genes with a percentage of false-positives (PFP) < 0.05 were considered differentially expressed between treatments and control in each experiment. This method has the advantage to identify genes with a response to the toxicants even when the absolute effect of the response was low. Because authors used sub-lethal concentrations of the toxicants, methods that use thresholds based on absolute fold change would not identify small changes in gene expression. Moreover, RP has proved to be a robust method for comparing microarray data from different sources and experiments. |
WBPaper00037113:CPF_DZN_16C_up-regulated
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