Transform lengthy academic papers into concise, structured 250-word abstracts.
中文简介正在准备中。当前显示原文说明。
Use when identifying stable sample subtypes from bulk expression matrices with ConsensusClusterPlus, including PAC-based model selection and consensus matrix/CDF visualization. NOT for: differential expression analysis, single-cell clustering workflows, or non-expression tables.
中文简介正在准备中。当前显示原文说明。
查看安装方法安装前可以查看交给 AI 代理的指令内容。
Use this skill when you need to identify stable sample subtypes from a bulk expression matrix with ConsensusClusterPlus, compare candidate clustering settings with PAC, and export consensus matrix/CDF visualizations.
Do not use this skill for differential expression analysis, single-cell clustering, or non-expression tabular data.
| Situation | File to Read | Purpose |
|---|---|---|
| Need algorithm details | references/algorithm.md | Consensus clustering, PAC scoring, and preprocessing assumptions |
| Need to run analysis | scripts/main.R | Execute: Rscript scripts/main.R --input_file ... --group_file ... |
| Encounter errors | references/troubleshooting.md | Common errors and solutions |
| Need CLI examples | references/cli-guide.md | Detailed CLI usage examples with verified local runs |
Rscript scripts/main.R \
--input_file ./expression_matrix.csv \
--group_file ./groups.csv \
--disease_group case \
--max_k 4 \
--output_dir ./output/ \
--gene_selection highly_variable \
--top_n 5000 \
--reps 1000 \
--p_item 0.8 \
--p_feature 1.0 \
--timeout_seconds 3600 \
--seed 42
| Short | Long | Type | Default | Description |
|---|---|---|---|---|
-i | --input_file | character | required | Expression matrix file (genes as rows, samples as columns) |
-g | --group_file | character | required | Group information file (sample ID + group columns) |
-d | --disease_group | character | case | Group label retained for clustering |
-k | --max_k | integer | 4 | Maximum cluster count to evaluate |
-o | --output_dir | character | ./output/ | Output directory |
-m | --gene_selection | character | highly_variable | Gene selection mode: highly_variable or custom |
-n | --top_n | integer | 5000 | Number of top variable genes to keep |
-l | --gene_list | character | NULL | Custom gene list file when gene_selection=custom |
-c | --center_data | logical | TRUE | Median-center each gene before clustering |
-r | --reps | integer | 1000 | Consensus resampling repetitions |
--p_item | double | 0.8 | Sample resampling proportion | |
--p_feature | double | 1.0 | Feature resampling proportion | |
-t | --timeout_seconds | integer | 3600 | Elapsed timeout in seconds |
-s | --seed | integer | 42 | Random seed for reproducibility |
Genes as rows, samples as columns, CSV/TSV/TXT format with gene ID in the first column.
,Sample01,Sample02,Sample03
TSPAN6,1.8479,1.8318,3.8276
TNMD,0.0349,0.0533,1.3889
Delimited text file with sample ID and group columns.
sample,group
Sample01,case
Sample02,control
Sample03,case
Optional plain text or single-column CSV file with one gene symbol per line.
TNMD
DPM1
SCYL3
| File | Description |
|---|---|
Cluster_res.csv | PAC summary for each distance/algorithm combination with is_best marking the selected model |
genes_for_clustering.csv | Selected genes and gene selection mode |
samples_for_clustering.csv | Samples retained after disease-group filtering |
result_<distance>_<algorithm>/ | Method-specific consensus outputs and PAC_scores.csv |
Consensus Matrix Plot.pdf | Consensus matrix heatmap for the optimal model |
CDF curve Plot.pdf | CDF curves for the optimal method |
session_info.txt | R session and package version info |
highly_variable or customRepeated subsampling is used to estimate cluster stability across candidate K values and clustering settings.
The proportion of ambiguous clustering is computed as CDF(0.9) - CDF(0.1) from lower-triangle consensus values. Lower PAC indicates more stable clustering.
highly_variable: rank genes by median absolute deviationcustom: use the intersection of the provided gene list and matrix row namesRscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-k 3 \
-r 20 \
-o output/example_basic \
-t 120
Rscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-m custom \
-l genes.csv \
-k 4 \
-r 20 \
-o output/example_custom \
-t 120
Rscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-c FALSE \
-k 3 \
-r 20 \
-o output/example_rawscale \
-t 120
| Error | Cause | Solution |
|---|---|---|
SKILL_FILE_NOT_FOUND | Input file does not exist | Check file path and permissions |
SKILL_MISSING_COLUMNS | Group file lacks sample/group columns | Verify column names in the group file |
SKILL_SAMPLE_MISMATCH | Sample names do not match | Ensure group file sample IDs match matrix columns |
SKILL_INVALID_PARAMETER | CLI value is invalid | Check allowed options and numeric ranges |
SKILL_INVALID_DATA | Too few samples/genes remain after filtering | Lower max_k or review the input data |
SKILL_TIMEOUT | Run exceeded the configured timeout | Increase timeout_seconds or reduce reps |
SKILL_DEPENDENCY_MISSING | Required R package is not installed | Install missing packages before rerunning |
IF error persists, READ: references/troubleshooting.md
# Check help
Rscript scripts/main.R --help
# Run analysis
Rscript scripts/main.R \
-i tests/data/expression_matrix.csv \
-g tests/data/groups.csv \
-d case \
-k 3 \
-r 20 \
-o output/example_basic \
-t 120
# Inspect selected model
cat output/example_basic/Cluster_res.csv
# Check output plots exist
ls -la output/example_basic
optparseset.seed() for reproducibilityrequireNamespace() dependency checksdata.table::fread() input readingSKILL.mdSKILL_* codesscripts/ directoryreferences/ directoryLast updated: 2026-04-17 | Version: 1.0.0
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Transform lengthy academic papers into concise, structured 250-word abstracts.
中文简介正在准备中。当前显示原文说明。
Precision editing tool that reduces abstract word count through intelligent compression techniques, maintaining scientific rigor while meeting strict journal and conference requirements.
中文简介正在准备中。当前显示原文说明。
Refines long medical academic texts into SCI-style unstructured Chinese and English abstracts; use when you need to condense drafts/reports/summaries into bilingual abstracts and generate Summary_Report.md.
中文简介正在准备中。当前显示原文说明。
Generates submission-ready Elsevier/SCI Highlights from manuscript text or extracted PDF/DOCX/TXT content. Use when a user needs 3-5 concise, evidence-grounded highlight bullets for a research paper, review, meta-analysis, case report, or bioinformatics manuscript.
中文简介正在准备中。当前显示原文说明。
Generates complete FAERS pharmacovigilance study designs for multi-drug or class-level safety comparison inside one predefined SOC or AE family using active comparators, disproportionality analysis, subgroup characterization, and reviewer-facing evidence control.
中文简介正在准备中。当前显示原文说明。
Analyze data with `adme-property-predictor` using a reproducible workflow, explicit validation, and structured outputs for review-ready interpretation.
中文简介正在准备中。当前显示原文说明。