DEG Analysis

Genomics Analysis

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Expression matrix file with genes as rows and samples as columns

Type of expression data

Type of gene identifier

Sample information file containing sample and group columns

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This option will load automatically after file upload

💾 Data Retention: Upload files retained for 10days, Result files retained for 15daysData will be retained after package expiration. Please download important data in time.

Task UUID:
Created At:
Analysis Progress

📋 Analysis Log


                            

Error Information

📁 Main Task Files (for subsequent analysis) (Inherited from parent)

Result Files

🔄 Adjust Parameters & Re-analyze

Only the following parameters can be adjusted in sub-task

💡 Threshold for adjusted p-value

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Tool Introduction & Use Cases

DEG Analysis is primarily used for differential expression analysis.

Differential expression gene analysis using DESeq2 or Limma, supporting counts/fpkm/tpm data types

Main Use Cases:

  • Compare treatment and control groups to identify up/down-regulated key genes or proteins
  • Assess the impact of drug treatment, gene knockout/overexpression on expression profiles
  • Provide high-confidence candidate sets for subsequent enrichment and pathway analysis

Key Features:

  • Differential expression statistics and significance assessment
  • Support for multiple testing correction (FDR/q-values)
  • Output standard results usable for volcano plots/heatmaps/enrichment

Parameter Details

ParameterMeaning & RecommendationsSettings
Sample Grouping FileExperimental Grouping/Control Setting: Defines comparison groups (two or more) and reference group. Recommendation: Reference group is typically "control/untreated". Ensure grouping matches sample annotations.
Required
Default: None
log2FC ThresholdLog2 Fold Change Threshold: Measures the magnitude of difference. For example, a threshold of 1 means you only care about genes with more than 2-fold upregulation or more than 50% downregulation. Recommendation: Typically set to 1 or 1.5. Higher values yield more dramatic differences.
Required
Default: 1
Adjusted P-value ThresholdMultiple Testing Correction Threshold (FDR/q): Controls false positive rates from multiple comparisons. Recommendation: Commonly 0.05; can be relaxed to 0.1 for smaller sample sizes or higher noise to maintain recall.
Required
Default: 0.05

Input File Requirements

Please ensure your input file format is correct, as this is fundamental to successful analysis. Typically, you need to provide a data matrix containing gene/protein expression values.

This tool does not currently provide sample files. Please refer to the common format: typically CSV or TXT files with the first column as gene/protein IDs, followed by expression values for each sample.

Frequently Asked Questions

Q: How long does the analysis take?

A: Estimated execution time is approximately 300 seconds, depending on your data size and current server load.

Q: What if the analysis fails?

A: If the analysis fails, your credits will not be deducted. First, check if your input file format matches the sample file, or adjust parameters based on error messages. If the problem persists, please contact us through the page's feedback function.

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