Use when estimating relative immune cell infiltration from a bulk expression matrix with a CIBERSORT-style nu-SVR deconvolution workflow based on an LM22 signature matrix, comparing one case group against one control group, and generating structured tables plus immune-fraction plots. NOT for single-cell RNA-seq, spatial data, clinical diagnosis, or workflows that require the original hosted CIBERSORT web service.
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scripts/main.R with the case and control groups.run_record.txt and output_manifest.txt after each run, including failed validation attempts.| Situation | File to Read | Purpose |
|---|---|---|
| Need to run the analysis | scripts/main.R | CLI entry point |
| Need algorithm details | references/algorithm.md | HQ reference workflow and result interpretation |
| Encounter an error | references/troubleshooting.md | Error codes and environment fixes |
| Need CLI examples or the baseline record | references/cli-guide.md | Example commands and validation notes |
| Need packaged test inputs | tests/data/ | Demo expression matrix, group file, and LM22 file |
Rscript scripts/main.R \
--input_file ./expression_matrix.csv \
--group_file ./group_info.csv \
--signature_file ./LM22.txt \
--case_group treatment \
--control_group control \
--output_dir ./output \
--qn false \
--seed 42| Short | Long | Type | Default | Description |
|---|---|---|---|---|
-i | --input_file | file | required | Expression matrix with genes as rows and samples as columns |
-g | --group_file | file | required | Group annotation table |
-a | --case_group | string | required | Case group label |
-b | --control_group | string | required | Control group label |
-o | --output_dir | dir | ./output | Output directory |
--signature_file | file | tests/data/LM22.txt when present | Signature matrix file | |
--sample_col | string/int | none | Optional sample column name or 1-based index | |
--group_col | string/int | none | Optional group column name or 1-based index | |
--gene_id_case | string | upper | Gene ID normalization: asis, upper, or lower | |
--auto_unlog | boolean | true | Apply 2^x only if the expression matrix passes a conservative log-scale heuristic | |
--min_mean_expression | numeric | 1 | Minimum mean expression before deconvolution | |
--perm | integer | 1000 | Permutation count for empirical p-value estimation; 0 keeps the run lightweight but records P-value as NA | |
--qn | boolean | true | Apply quantile normalization to the mixture matrix | |
--svm_cores | integer | 1 | Worker count for the nu-SVR model selection step | |
--make_plots | boolean | true | Generate PDF plots | |
--plot_width | numeric | 16 | Default plot width in inches | |
--plot_height | numeric | 10 | Default plot height in inches | |
-s | --seed | integer | 42 | Random seed |
-t | --timeout_seconds | integer | 0 | Optional timeout in seconds; 0 disables it |
--verbose | boolean | true | Print progress logs |
CSV or TSV. The first column must contain gene identifiers. Remaining columns must be numeric sample-level expression values.
When --auto_unlog=true, the workflow reports summary statistics and applies 2^x only if the matrix passes a conservative log-scale heuristic. If the matrix is ambiguous, the values are left unchanged and the startup log explains why.
If duplicate gene identifiers are present, they are consolidated after gene-ID normalization by taking the per-sample maximum before downstream filtering and deconvolution.
gene,Sample1,Sample2,Sample3
TP53,10.2,8.5,9.1
CXCL9,4.3,6.1,5.7CSV or TSV with one sample column and one group column.
sample,group
Sample1,control
Sample2,treatment
Sample3,treatmentThe packaged default is tests/data/LM22.txt. A custom signature matrix must contain one gene column followed by immune-cell signature columns.
All immune-cell signature columns must be numeric and finite. If duplicate gene identifiers are present, they are consolidated by taking the per-cell-type maximum before gene intersection.
| File | Description |
|---|---|
data/cibersort_input.rds | Serialized aligned input matrices used by the local algorithm |
data/cibersort_null_distribution.rds | Serialized permutation null distribution |
data/cibersort_result.rds | Serialized result object with cell fractions, metrics, runtime settings, and heatmap rendering metadata |
table/CIBERSORT_Results.csv | Full result table in CSV format |
table/CIBERSORT-Results.txt | Full result table in tab-delimited text format |
table/cibersort_cell_fractions_wide.csv | Wide-format immune cell fraction table |
table/cibersort_cell_fractions_long.csv | Long-format immune cell fraction table |
table/cibersort_group_compare.csv | Case-vs-control comparison summary |
table/cibersort_quality_metrics.csv | Sample-level P-value, Correlation, and RMSE table |
table/immune_cell_correlation_matrix.csv | Spearman correlation matrix across immune cell types |
table/immune_cell_correlation_pvalue.csv | P-value matrix aligned to the correlation matrix |
plot/immune_cell_composition_sample.pdf | Sample-level stacked composition plot when --make_plots=true |
plot/immune_group_boxplot.pdf | Group comparison boxplot when --make_plots=true |
plot/immune_correlation_heatmap.pdf | Immune-cell correlation heatmap when --make_plots=true |
session_info.txt | R session information |
output_manifest.txt | Append-only output manifest for successful and failed runs |
run_record.txt | Append-only structured run record, including runtime notes and failed-run summaries |
When --make_plots=false, the plot/ directory may still exist as part of the standard output layout, but no PDF plot files are written.
When --perm=0, the workflow logs a warning and completes without empirical permutation testing, so the P-value column is recorded as NA.
When a rerun targets an existing --output_dir and then fails validation or execution, the previous successful payload is preserved and the failure is appended to run_record.txt and output_manifest.txt.
| Error Code | Meaning | Solution |
|---|---|---|
SKILL_FILE_NOT_FOUND | An input file or signature matrix was not found | Check the file path and rerun |
SKILL_MISSING_COLUMNS | A required column is missing | Fix the input schema |
SKILL_EMPTY_DATA | No usable genes, samples, or deconvolution outputs remain | Check the data, filtering, or signature overlap |
SKILL_INVALID_PARAMETER | A CLI parameter is missing or invalid | Review the argument table and input values |
SKILL_SAMPLE_MISMATCH | Expression samples and group annotations do not align | Harmonize sample identifiers |
SKILL_PACKAGE_NOT_FOUND | A required R package is missing | Install the missing package |
SKILL_TIMEOUT | The configured time limit was exceeded | Increase --timeout_seconds or set it to 0 |
If the error persists, READ: references/troubleshooting.md
This skill accepts:
Do not use this skill for:
If the user's request is outside this scope, do not proceed with the workflow. Instead respond:
"cibersort-immune-infiltration-analysis is designed for local CIBERSORT-style immune deconvolution from a bulk expression matrix with one case group and one control group. Your request appears to be outside this scope. Please provide compatible bulk-expression inputs and group labels, or use a more appropriate tool for your task."
Rscript scripts/main.R --help
Rscript tests/run_tests.R
Rscript tests/test_skill.RValidated packaged test path:
Rscript scripts/main.R \
--input_file tests/data/expression_matrix.csv \
--group_file tests/data/group_info.csv \
--signature_file tests/data/LM22.txt \
--case_group Tumor \
--control_group Healthy \
--output_dir tests/output \
--perm 25 \
--qn false \
--svm_cores 1 \
--seed 42Container note:
--qn false because preprocessCore::normalize.quantiles() may trigger environment-level thread failures in some containers.references/cli-guide.md.tests/run_tests.R also checks that a failed rerun does not erase an existing successful payload directory.63c61d3
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