生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
日本語の概要は準備中です。原文の説明を表示しています。
Add p-value brackets, significance asterisks, and effect-size annotations to distribution plots using ggpubr, ggsignif, and statannotations with correct test selection (parametric vs non-parametric vs paired), multiple-testing adjustment, and rendering of negative results. Use when a boxplot/violin/raincloud needs in-figure statistical comparisons between groups.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Reference examples tested with: ggpubr 0.6+, ggsignif 0.6+, rstatix 0.7+, statannotations 0.6+ (Python), seaborn 0.13+.
Before using code patterns, verify installed versions match. If versions differ:
packageVersion('<pkg>') then ?function_namepip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Add p-values to my plot" -> Render pairwise group comparisons as brackets with the correct statistical test (parametric vs non-parametric, paired vs unpaired, independent vs nested), adjusted for multiple testing, with rendering of significance as either numerical p OR asterisks. The choices that matter: which test is appropriate for the data, what multiple-testing adjustment applies, and whether to show n.s. (non-significant) results.
ggpubr::stat_compare_means, ggsignif::geom_signif, rstatix::t_test/wilcox_teststatannotations.Annotator, scipy.stats directlyTool defaults are NOT data-appropriate. ggpubr::stat_compare_means(method='t.test') uses Welch's two-sample t-test assuming approximate normality and unequal variances. This is wrong when:
method='wilcox.test').paired = TRUE).The bracket-and-asterisk visual is the same; the underlying statistics are not. Choose the test deliberately.
| Question | Recommended test | Function |
|---|---|---|
| 2 unpaired groups, normal, N≥30 | Welch t-test | t.test(), stat_compare_means(method='t.test') |
| 2 unpaired groups, non-normal or small N | Mann-Whitney U (Wilcoxon rank-sum) | wilcox.test(), stat_compare_means(method='wilcox.test') |
| 2 paired groups | Paired t-test OR Wilcoxon signed-rank | paired = TRUE |
| 3+ groups, normal | One-way ANOVA + Tukey HSD post-hoc | aov(), TukeyHSD() |
| 3+ groups, non-normal | Kruskal-Wallis + Dunn post-hoc | kruskal.test(), dunn.test() |
| Nested data (cells in patients) | Linear mixed model | lme4::lmer() |
| Time-course / repeated measures | Repeated-measures ANOVA OR LMM | nlme::lme() |
| Two-way factorial | Two-way ANOVA + interaction term | aov(y ~ a*b) |
| Survival / time-to-event | Log-rank, NOT t-test | survdiff() |
| Categorical outcome | Chi-square OR Fisher exact | chisq.test(), fisher.test() |
For pairwise comparisons among K groups, there are K(K-1)/2 unadjusted p-values. Without adjustment, family-wise error rate inflates rapidly:
# rstatix supports per-comparison adjustment
library(rstatix)
df %>%
pairwise_wilcox_test(value ~ group, p.adjust.method = 'bonferroni') %>%
add_xy_position(x = 'group')
p.adjust.method options:
'bonferroni' — strictest; controls FWER'holm' — stepwise Bonferroni; uniformly more powerful than Bonferroni'BH' (Benjamini-Hochberg) — FDR; less strict than FWER; standard for genomics'fdr' — alias for BHFor figure annotations, holm is the modern default — controls FWER and is more powerful than bonferroni. For a small number of pre-planned comparisons (≤3), Bonferroni is fine.
Goal: Add per-comparison p-value brackets between groups on a distribution plot, using a test appropriate to data shape and adjusting for multiple comparisons.
Approach: Build the base plot with ggboxplot(); add stat_compare_means() with explicit method, comparisons, p.adjust.method, and label arguments; render as asterisks (p.signif) for terse display or numeric (p.format) for precise display.
library(ggpubr)
# Default boxplot + p-value bracket(s)
ggboxplot(df, x = 'group', y = 'value', color = 'group',
add = 'jitter', palette = 'npg') +
stat_compare_means(method = 'wilcox.test', # explicit; default is t-test
comparisons = list(c('Control', 'Treatment'),
c('Control', 'Vehicle'),
c('Treatment', 'Vehicle')),
label = 'p.signif', # 'p.signif' for asterisks; 'p.format' for numeric
p.adjust.method = 'holm',
method.args = list(alternative = 'two.sided'))
For an overall test plus pairwise:
# Overall + per-comparison
ggboxplot(df, x = 'group', y = 'value', color = 'group') +
stat_compare_means(method = 'kruskal.test', # overall test
label.y = 1.05 * max(df$value)) +
stat_compare_means(comparisons = pairs,
method = 'wilcox.test',
p.adjust.method = 'holm',
label = 'p.signif')
library(ggsignif)
ggplot(df, aes(group, value, fill = group)) +
geom_boxplot() +
geom_signif(comparisons = list(c('Control', 'Treatment')),
test = 'wilcox.test',
map_signif_level = TRUE, # asterisks vs numeric p
step_increase = 0.1) +
scale_fill_manual(values = c('#0072B2', '#D55E00'))
map_signif_level = TRUE converts p-values to asterisks per Wasserstein-Lazar 2016 convention:
*** p < 0.001** p < 0.01* p < 0.05ns p ≥ 0.05For literal p-values, set FALSE.
import seaborn as sns
from statannotations.Annotator import Annotator
ax = sns.boxplot(x='group', y='value', data=df, palette=['#0072B2', '#D55E00', '#009E73'])
pairs = [('Control', 'Treatment'),
('Control', 'Vehicle'),
('Treatment', 'Vehicle')]
annotator = Annotator(ax, pairs, data=df, x='group', y='value')
annotator.configure(test='Mann-Whitney', # 't-test_ind', 't-test_paired', 'Wilcoxon', etc
comparisons_correction='holm',
text_format='star', # 'star', 'simple', 'full'
line_height=0.02,
text_offset=0.5)
annotator.apply_and_annotate()
Trigger: stat_compare_means(method='t.test') (default) on log-distributed expression.
Mechanism: t-test assumes approximate normality; non-normal data with small N inflates Type-I.
Symptom: Significant p where rank test gives p > 0.05.
Fix: Switch to method='wilcox.test' for non-normal or small-N data. Verify normality with Shapiro-Wilk if borderline.
Trigger: Multiple bracket annotations with raw p-values.
Mechanism: K(K-1)/2 comparisons inflate FWER without adjustment.
Symptom: All-pairwise significant at nominal 0.05; doesn't replicate.
Fix: p.adjust.method = 'holm' (or 'bonferroni' or 'BH'). Document choice.
Trigger: Before/after measurements in same subjects, tested with unpaired t-test.
Mechanism: Ignores within-subject correlation; loses power.
Symptom: Non-significant p where paired test gives significant.
Fix: paired = TRUE (R) or t-test_paired (statannotations). Verify subjects are correctly matched.
Trigger: Hundreds of cells per patient, tested as if each cell is independent.
Mechanism: Pseudoreplication — within-patient correlation ignored; p-values dramatically over-significant.
Symptom: p < 1e-50 from a dataset where the actual N is ~10 patients.
Fix: Linear mixed model (lme4::lmer(value ~ group + (1|patient_id))); aggregate to per-patient median first; or pseudobulk.
Trigger: label = 'p.signif' exclusively.
Mechanism: Reader cannot recover the actual p-value.
Symptom: Reviewer asks for exact p; not in figure or supplementary.
Fix: Either show numeric p (label = 'p.format') or include test results table in supplementary.
Trigger: Showing only significant brackets, omitting non-significant.
Mechanism: Selective reporting biases interpretation.
Symptom: Reader assumes untested pairs were significant.
Fix: Either annotate all comparisons (with n.s. for non-significant) OR pre-specify which pairs are tested in the legend/caption.
Trigger: Conclusion "highly significant difference" from p = 1e-10 on a tiny effect.
Mechanism: Large N inflates significance for trivial differences.
Symptom: Effect size negligible despite extreme p.
Fix: Always report effect size (Cohen's d, Cliff's delta, median difference with CI) alongside p. The bracket should convey direction AND magnitude, not just significance.
| Pattern | Cause | Action |
|---|---|---|
| t-test significant; Wilcoxon n.s. | Outliers driving t-test; rank test robust | Trust Wilcoxon for non-normal data |
| Unpaired n.s.; paired significant | Within-subject correlation matters | Use paired if subjects are matched |
| Pairwise all-significant; ANOVA n.s. | Multiple-testing inflation in pairwise | ANOVA / Kruskal-Wallis is the overall test; pairwise post-hoc only after omnibus significant |
| Pseudo-replicated p < 1e-50; LMM p = 0.1 | Pseudoreplication | LMM is correct; pseudo-replicated p is meaningless |
| Bonferroni-adjusted n.s.; raw p < 0.05 | Adjustment correctly identified borderline | Trust adjusted; document the test family |
| Threshold | Value | Source |
|---|---|---|
| α for FWER control | 0.05 family-wise | Standard |
| α for FDR control | 0.05 expected FDR (BH) | Benjamini-Hochberg 1995 |
| Asterisk convention | * <0.05, ** <0.01, *** <0.001 | Common practice |
| Bonferroni cutoff | 0.05 / K(K-1)/2 | Standard |
| Holm step-down | better than Bonferroni for all K | Holm 1979 |
| FDR (BH) | less strict than FWER | Genomics standard |
| Error / symptom | Cause | Solution |
|---|---|---|
| Reviewer asks "why t-test?" | Default not justified | Pre-justify test choice |
| Many pairwise-significant; doesn't replicate | No multiple-testing adjustment | Holm or BH |
| Effect "highly significant" but tiny | Large N inflates p | Report effect size |
| Asterisks only; no p-values | label = 'p.signif' exclusively | Show p.format OR provide table |
| Pseudoreplication inflated p | Cells treated as independent | LMM or pseudobulk |
| n.s. comparisons hidden | Selective reporting | Annotate all pre-specified pairs |
| Numeric p truncated to '<2.22e-16' | R default precision | Manual formatting or report as < 2e-16 |
まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
日本語の概要は準備中です。原文の説明を表示しています。
Predicts ADMET properties using ADMETlab 3.0 (119 endpoints with uncertainty), ADMET-AI, DeepChem MolNet, and chemprop D-MPNN with explicit handling of OECD QSAR principles, applicability domain assessment, calibration, hERG/CYP/AMES gold-standard endpoints, and PAINS / Lipinski / Ro5 / Veber / BBB druglikeness filters. Use when filtering compounds for drug-likeness, prioritizing leads by predicted safety, or building an in-house ADMET QSAR model.
日本語の概要は準備中です。原文の説明を表示しています。
Trim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
日本語の概要は準備中です。原文の説明を表示しています。
Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
日本語の概要は準備中です。原文の説明を表示しています。
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
日本語の概要は準備中です。原文の説明を表示しています。
Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
日本語の概要は準備中です。原文の説明を表示しています。