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。
Build Sankey, alluvial, river, and CONSORT-style flow diagrams to visualize cohort transitions, cell-state changes, or pipeline filtering using ggalluvial, networkD3, plotly, and consort. Use when showing how entities move between categories across timepoints (cell states, drug response classes, patient flow through a trial) or filtering pipelines (variants filtered through QC stages).
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: ggalluvial 0.12+, networkD3 0.4+, plotly 4.10+, consort 0.2+ (CONSORT diagrams), pySankey 0.0.1+.
Before using code patterns, verify installed versions match. If versions differ:
packageVersion('<pkg>') then ?function_namepip show <package> then help(module.function)If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Show how things flow between categories" -> Render entities as ribbons whose width encodes count, flowing between ordered columns of categories. Sankey emphasizes total flow magnitude; alluvial emphasizes per-entity continuity (each row's path is traceable); CONSORT formalizes the trial-filtering convention. The decision space: which method (Sankey vs alluvial vs CONSORT), how to order categories within each column, and whether to highlight specific entity trajectories.
ggalluvial::geom_alluvium, networkD3::sankeyNetwork, consort::consort_plotplotly.graph_objects.Sankey, pySankeySankey plots show flow from sources to sinks; each ribbon represents an aggregate count. The horizontal direction is "flow." Use for energy flows, web-traffic funnels, cohort dropouts.
Alluvial plots track individual entities through multiple ordered category columns (axes). Each row of input data becomes a continuous ribbon; intersections at each axis show counts in each category. Use for cell-state transitions across timepoints, drug-response trajectories, longitudinal class changes.
A Sankey shows "100 cells became neuron, 50 became glia"; an alluvial shows "of the 100 that became neurons at t2, 80 came from the proliferating pool at t1." Different encoding, different scientific story.
| Use case | Recommended | Tool |
|---|---|---|
| Single timepoint, source-to-sink flow | Sankey | networkD3, plotly |
| Multi-timepoint entity trajectories | Alluvial | ggalluvial |
| Clinical trial patient flow | CONSORT (formal vertical box-and-arrow) | consort R package |
| Variant filtering pipeline | CONSORT-style flow | consort or manual diagrammeR |
| Cell-state transitions (scRNA timepoints) | Alluvial OR Sankey if 2 timepoints | ggalluvial |
| Drug response class changes | Alluvial | ggalluvial |
| Gene-set membership across conditions | UpSet (alternative) | data-visualization/upset-plots |
Goal: Visualize entity (e.g., cell, patient) trajectories across multiple ordered axes with ribbon-width = count.
Approach: Reshape to "lodes" (long) format with one row per entity-stratum, or "alluvia" (wide) format with one row per entity; use geom_alluvium for ribbons and geom_stratum for column boxes.
library(ggalluvial)
library(ggplot2)
# Wide (alluvia) format: one row per entity
df_wide <- data.frame(
entity_id = 1:1000,
t1 = sample(c('A', 'B', 'C'), 1000, replace = TRUE),
t2 = sample(c('A', 'B', 'C'), 1000, replace = TRUE),
t3 = sample(c('A', 'B', 'C'), 1000, replace = TRUE))
ggplot(df_wide, aes(axis1 = t1, axis2 = t2, axis3 = t3)) +
geom_alluvium(aes(fill = t1), alpha = 0.7, width = 1/6) +
geom_stratum(width = 1/6, fill = 'grey90', color = 'black') +
geom_text(stat = 'stratum', aes(label = after_stat(stratum)), size = 3) +
scale_x_discrete(limits = c('t1', 't2', 't3')) +
scale_fill_manual(values = c('#0072B2', '#D55E00', '#009E73')) +
labs(y = 'Entities', x = NULL) +
theme_classic()
aes(fill = t1) colors each ribbon by its starting class — common pattern for "where did this end up cluster come from?" stories.
library(networkD3)
# Nodes and links
nodes <- data.frame(name = c('Source A', 'Source B', 'Sink X', 'Sink Y', 'Sink Z'))
links <- data.frame(source = c(0, 0, 1, 1),
target = c(2, 3, 3, 4),
value = c(40, 30, 50, 20))
sankeyNetwork(Links = links, Nodes = nodes,
Source = 'source', Target = 'target', Value = 'value',
NodeID = 'name',
colourScale = JS('d3.scaleOrdinal(d3.schemeCategory10);'),
fontSize = 12, nodeWidth = 30, height = 400, width = 700)
networkD3 produces interactive HTML — drag nodes, hover for values. For static publication figure, screenshot or export via webshot2.
import plotly.graph_objects as go
fig = go.Figure(go.Sankey(
node=dict(label=['Source A', 'Source B', 'Sink X', 'Sink Y', 'Sink Z'],
color=['#0072B2', '#56B4E9', '#D55E00', '#E69F00', '#009E73']),
link=dict(source=[0, 0, 1, 1],
target=[2, 3, 3, 4],
value=[40, 30, 50, 20],
color=['rgba(0,114,178,0.4)'] * 4)))
fig.update_layout(title='Flow', font_size=12)
fig.write_html('sankey.html')
fig.write_image('sankey.pdf') # requires Kaleido (NOT orca; orca is EOL)
CONSORT 2010 (Schulz 2010 BMJ 340:c332) is the canonical clinical-trial flow diagram. The consort R package implements the structure:
library(consort)
# Trial enrollment flow
g <- add_box(txt = c('Assessed for eligibility (n=200)'))
g <- add_side_box(g, txt = c('Excluded (n=50)\n - Not meeting criteria (n=30)\n - Declined (n=15)\n - Other (n=5)'))
g <- add_box(g, txt = c('Randomized (n=150)'))
g <- add_split(g, txt = c('Allocated to intervention (n=75)\n - Received as allocated (n=70)\n - Did not receive (n=5)',
'Allocated to control (n=75)\n - Received as allocated (n=73)\n - Did not receive (n=2)'))
g <- add_box(g, txt = c('Lost to follow-up (n=2)\nDiscontinued (n=3)',
'Lost to follow-up (n=1)\nDiscontinued (n=2)'))
g <- add_box(g, txt = c('Analysed (n=75)\nExcluded from analysis (n=0)',
'Analysed (n=75)\nExcluded from analysis (n=0)'))
plot(g)
CONSORT is a required element in randomized trial publication (CONSORT 2010 statement, item 13a).
Trigger: Multi-timepoint cell-state data plotted as Sankey instead of alluvial.
Mechanism: Sankey collapses to source-sink summary; loses entity-trajectory continuity.
Symptom: Reader sees "cluster A -> 50% to B, 50% to C" but cannot trace individual trajectories.
Fix: Use ggalluvial for multi-axis trajectories; Sankey for single-step source-to-sink.
Trigger: Default ggalluvial ordering by frequency.
Mechanism: Categories shuffle position across columns; ribbons cross excessively.
Symptom: Visual spaghetti; hard to follow.
Fix: Set explicit factor levels (factor(t1, levels = c('A', 'B', 'C'))) AND consider ggalluvial's lode.guidance to minimize crossings.
Trigger: geom_alluvium(aes(fill = t3)) for a "where did these come from" story.
Mechanism: Color encodes the wrong axis; readers misinterpret.
Symptom: Story is "where did final cluster Z come from" but ribbons are colored by Z — every ribbon to Z is the same color.
Fix: aes(fill = t1) if origin matters; aes(fill = t3) if destination matters.
Trigger: Skipping "Lost to follow-up" or "Excluded from analysis" boxes.
Mechanism: CONSORT 2010 requires reporting at each stage.
Symptom: Submission flagged for non-compliance with CONSORT 2010 item 13a.
Fix: Use consort package which scaffolds the required structure; cross-check against CONSORT 2010 statement.
Trigger: Source-to-target sums don't balance.
Mechanism: plotly Sankey requires conservation: sum of in-flows = sum of out-flows at each non-terminal node.
Symptom: Layout renders but node sizes look wrong; ribbons stretch/compress incorrectly.
Fix: Verify upstream data: per-node sum(value where target=node) == sum(value where source=node) for internal nodes.
Trigger: fig.write_image('sankey.pdf') without kaleido installed.
Mechanism: plotly defaults to Kaleido for static export since orca EOL; kaleido is optional dependency.
Symptom: No file written; no error in some plotly versions.
Fix: pip install kaleido; verify with import kaleido.
| Pattern | Cause | Action |
|---|---|---|
| ggalluvial and networkD3 show different orderings | Different default stratum/node ordering | Set explicit factor levels / node order |
| CONSORT box counts don't sum | Box-content arithmetic error | Audit each box; consort package enforces structure |
| Cells appear/disappear between alluvial axes | Missing data in some timepoints | Decide: drop entities with NA; OR add "Missing" category |
| Threshold | Value | Source |
|---|---|---|
| Max categories per column for legibility | 5-7 | Visualization practical |
| Max axes for alluvial | 4-5 | Above this ribbons too crossed |
| CONSORT requirement | Required for RCTs | Schulz 2010 CONSORT 2010 |
| Error / symptom | Cause | Solution |
|---|---|---|
| Excessive ribbon crossing | Categories unordered | Explicit factor levels; lode.guidance |
| Trajectories not traceable | Sankey used instead of alluvial | Switch to ggalluvial |
| CONSORT non-compliant | Missing required boxes | Use consort package |
| Sankey node sizes wrong | Flow not conserved | Audit source-target sums |
| plotly static export blank | kaleido not installed | pip install kaleido |
| Color story unclear | Wrong axis for fill | Decide origin vs destination story |
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。