omicverse-single-cell-differential-expression

name	omicverse-single-cell-differential-expression
description	Run OmicVerse single-cell differential expression analysis as a reusable, triggerable skill. Use when comparing conditions inside one or more cell types in AnnData, choosing between Wilcoxon, t-test, and memento backends, or adapting a related notebook into a repeatable DEG workflow.

OmicVerse Single-Cell Differential Expression

Goal

Turn notebook-style OmicVerse DEG analysis into a compact execution spine for condition-vs-condition comparisons inside selected cell types. Keep this skill focused on DEG only; differential abundance and compositional analysis are a separate job with a different input contract and backend surface.

Quick Workflow

1. Inspect the input AnnData, the condition column, the cell-type column, and whether raw counts are available in adata.raw or adata.layers["counts"].
2. Choose a DEG backend before running anything: wilcoxon or t-test for the scanpy rank-gene path, memento-de for the count-aware memento path.
3. Subset to the required cell types with celltype_key and celltype_group; leave celltype_group=None only when you really want all cell types pooled into one DEG run.
4. Run DEG.run(...) with an explicit max_cells policy and method-specific kwargs when using memento.
5. Collect results with get_results(), then verify the expected statistical columns and expression-percentage columns before saving or plotting.

Interface Summary

• ov.single.DEG(adata, condition, ctrl_group, test_group, method='wilcoxon', use_raw=None) initializes the wrapper.
• method branches are wilcoxon, t-test, and memento-de.
• use_raw=None auto-detects adata.raw; if raw exists, the wrapper copies adata.raw.X into a fresh object and uses that matrix for DEG.
• DEG.run(celltype_key, celltype_group=None, max_cells=100000, **kwargs) subsets by cell type and dispatches to the selected backend.
• wilcoxon and t-test normalize and log-transform only when the active matrix still looks integer-valued.
• memento-de expects count-like input; if X is not integer-valued, the wrapper first looks for adata.layers["counts"] and otherwise tries count recovery from log-normalized values.
• memento-specific kwargs are passed through run(...); the notebook used capture_rate, num_cpus, and num_boot.
• DEG.get_results() returns a DEG table and augments it with baseMean, pct_ctrl, pct_test, and pct_diff.

Stage Selection

• Use method='wilcoxon' when you want the notebook's fast nonparametric path on one or more selected cell types.
• Use method='t-test' only when a t-test is acceptable for the data distribution and normalization state.
• Use method='memento-de' when the user explicitly wants memento's differential-mean path or needs the extra branch-specific kwargs.
• Keep celltype_group explicit for targeted comparisons such as one lineage or cluster; set it to None only when a pooled all-cell-type DEG run is actually intended.
• Treat violin plots as optional reporting after DEG, not as part of the reusable execution contract.

Input Contract

• Start from an AnnData object with a condition column in obs.
• Provide control and test labels that exist in that condition column.
• Provide a cell-type column for celltype_key.
• Prefer preserving raw counts in adata.raw or adata.layers["counts"], especially for memento-de.
• Expect the wrapper to coerce dense matrices to CSR internally.

Minimal Execution Patterns

import omicverse as ov

deg = ov.single.DEG(
    adata,
    condition="condition",
    ctrl_group="Control",
    test_group="Salmonella",
    method="wilcoxon",
)
deg.run(
    celltype_key="cell_label",
    celltype_group=["TA"],
    max_cells=100000,
)
res = deg.get_results()

deg = ov.single.DEG(
    adata,
    condition="condition",
    ctrl_group="Control",
    test_group="Salmonella",
    method="memento-de",
    use_raw=False,
)
deg.run(
    celltype_key="cell_label",
    celltype_group=["TA"],
    capture_rate=0.07,
    num_cpus=12,
    num_boot=5000,
)
res = deg.get_results()

Constraints

• Do not merge DEG and DCT into one skill at execution time; they are independently triggerable and use different backends.
• Do not assume the notebook's example cell type or example genes are universal defaults.
• Do not leave method implicit; branch choice changes both the statistical engine and the data expectations.
• Do not claim that memento-de ran on raw counts unless you actually confirmed raw counts, a counts layer, or successful count recovery.
• Keep smoke and acceptance commands shell-agnostic. Do not rely on zsh-specific syntax, shell startup files, or shell-only features when a direct ${PYTHON} script.py command is enough.
• Do not put local paths or environment names into the reusable instructions.

Validation

• Check that the selected control and test labels both remain after subsetting.
• Check that DEG.run(...) used the intended cell-type subset.
• For wilcoxon and t-test, check that the result table contains at least log2FC, pvalue, padj, qvalue, baseMean, pct_ctrl, pct_test, and pct_diff.
• For memento-de, check that the result table still gains baseMean, pct_ctrl, pct_test, and pct_diff after get_results().
• If the dataset is large, say whether max_cells caused downsampling.
• If only a bounded smoke path was run, say so explicitly.

Resource Map

• Use the branch selection notes when choosing the DEG backend or deciding whether all cell types should be pooled.
• Use the source grounding notes when you need the live signatures, defaults, or branch-specific behavior.
• Use the notebook map when tracing which tutorial cells became which reusable instruction.
• Use the compatibility notes when notebook prose and current runtime behavior diverge.