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。
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Resolve the architecture of focal oncogene amplifications — extrachromosomal DNA (ecDNA), breakage-fusion-bridge (BFB) cycles, homogeneously staining regions (HSR), and linear amplification — from whole-genome sequencing with AmpliconArchitect, the AmpliconSuite pipeline, and AmpliconClassifier. Covers copy-number seed selection, breakpoint-graph reconstruction, balanced-flow optimization, ecDNA classification, and the limits of depth-only amplification calls. Use when a focal amplification needs structural characterization, when distinguishing ecDNA from chromosomal amplification, suspecting ecDNA-driven oncogene amplification or therapy resistance, or selecting copy-number seeds for amplicon reconstruction.
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Reference examples tested with: AmpliconSuite-pipeline 1.3+, AmpliconArchitect 1.3+, AmpliconClassifier 1.2+, CNVkit 0.9.10+, Python 3.10+, samtools 1.19+.
Before using code patterns, verify installed versions match. If versions differ:
AmpliconSuite-pipeline.py --help, amplicon_classifier.py --help$AA_DATA_REPO reference download and a Mosek license (free for academic use); confirm both are configured before runningVerify the reference build — AmpliconArchitect was historically hg19-centric; GRCh38 support and data repos exist but the build must be set explicitly and consistently.
"This oncogene is amplified — but how, structurally" -> A depth caller reports "high focal amplification" and stops. The biology depends entirely on the architecture: extrachromosomal DNA (ecDNA) behaves utterly differently from a chromosomal homogeneously staining region. Resolving architecture needs the breakpoint graph, not depth.
AmpliconSuite-pipeline.py (end-to-end), AmpliconArchitect (graph reconstruction), AmpliconClassifier (architecture call)| Class | Structure | Behavior | Why it matters |
|---|---|---|---|
| ecDNA | Circular, episomal, no centromere | Hundreds of copies; unequal mitotic segregation; rapid CN adaptation | Drives oncogene overexpression, intratumor heterogeneity, therapy resistance; ~14% of cancers |
| BFB | Chromosomal, fold-back inversions | Stepwise CN gradient toward telomere | Distinct breakpoint signature; bounded amplification |
| HSR | Linear, integrated chromosomally | Stable inheritance | Chromosomal — segregates evenly, unlike ecDNA |
| Linear/simple | Tandem or simple amplification | Modest copy gain | Often passenger-scale; lowest oncogenic concern |
ecDNA is the highest-stakes call: because it lacks a centromere it segregates unequally, so copy number can surge under selection — a structural basis for resistance. Depth alone cannot distinguish ecDNA from an HSR; both look like a high-amplitude focal gain.
| Signal | Interpretation |
|---|---|
| Very high focal copy number (CN >> 10) at an oncogene | Consistent with ecDNA; not specific |
| Amplicon spanning multiple non-contiguous genomic segments | Suggestive — ecDNA often fuses distal regions |
| Breakpoint graph forms a closed cycle with balanced flow | AmpliconArchitect signature of circular structure |
| Highly variable per-cell copy number (single-cell / FISH) | Hallmark of unequal ecDNA segregation |
| Co-amplified enhancers distal to the oncogene | ecDNA can hijack regulatory elements |
AmpliconArchitect does not call amplifications from scratch — it reconstructs the architecture of the regions it is seeded with. The pipeline is: (1) call copy number and select high-CN focal seeds, (2) AmpliconArchitect builds the breakpoint graph and optimizes a balanced flow, (3) AmpliconClassifier labels each amplicon ecDNA / BFB / HSR / linear.
# End-to-end: AmpliconSuite-pipeline runs CNVkit seeding, AmpliconArchitect, and
# AmpliconClassifier in sequence.
AmpliconSuite-pipeline.py \
-s sample_id \
-t 8 \
--bam tumor.bam \
--ref GRCh38 \
--run_AA --run_AC
# Output: per-amplicon breakpoint graphs, cycles files, and an AmpliconClassifier
# table assigning each amplicon an architecture class.
Supplying explicit seeds (recommended when a vetted CNV callset exists):
# Seeds: a BED of high-copy focal regions (e.g. from cnvkit-analysis), filtered to
# CN above the seed threshold and to focal (not arm-level) size.
AmpliconSuite-pipeline.py -s sample_id -t 8 --bam tumor.bam --ref GRCh38 \
--cnv_bed focal_seeds.bed --run_AA --run_AC
Trigger: Seeding AmpliconArchitect with a noisy CNV callset, a flat-reference tumor-only callset, or arm-level segments.
Mechanism: AmpliconArchitect reconstructs the architecture of exactly the regions it is seeded with; false high-CN seeds generate spurious amplicons, and arm-level seeds dilute the focal signal.
Symptom: Implausible amplicons at no known oncogene; amplicons spanning whole arms; classifier output dominated by low-confidence calls.
Fix: Seed only vetted, focal, high-CN regions. Build the CNV callset from a proper panel of normals (see cnvkit-analysis); filter to focal size and CN above the seed threshold before passing to AA.
Trigger: Labeling a high-amplitude focal gain "ecDNA" without breakpoint-graph evidence.
Mechanism: ecDNA and a chromosomal HSR both present as high focal copy number; only the breakpoint graph (a closed cycle with balanced flow) distinguishes them.
Symptom: ecDNA claimed from a CNVkit/GATK profile; no graph, no cycle.
Fix: Require AmpliconArchitect graph reconstruction and an AmpliconClassifier ecDNA call. Where feasible, confirm with orthogonal evidence — FISH, single-cell copy number (variable per-cell CN), or optical mapping.
Trigger: BAM aligned to one build, --ref or $AA_DATA_REPO set to another.
Mechanism: Coordinates and the bundled annotation diverge; breakpoints and genes are mis-assigned.
Symptom: Amplicons at wrong loci; AA errors on contig names.
Fix: Set --ref to match the BAM's build and confirm the corresponding $AA_DATA_REPO is installed; AA was historically hg19-centric, so GRCh38 must be explicit.
Trigger: Expecting a fully resolved amplicon structure from short-read WGS on a highly rearranged amplicon.
Mechanism: Short reads cannot phase long-range structure or traverse repeats; complex amplicons (many junctions, segmental duplications) are only partially reconstructed.
Symptom: Fragmented breakpoint graph; ambiguous or "unknown" classifier calls on a clearly amplified locus.
Fix: Treat short-read amplicon structure as a hypothesis for the most complex cases; confirm with optical mapping (AmpliconReconstructor) or long-read sequencing.
Trigger: Low-coverage WGS or degraded FFPE DNA.
Mechanism: Breakpoint detection needs sufficient discordant/split-read support; FFPE artifacts add false junctions.
Symptom: Missing junctions; noisy graph; unstable classification.
Fix: Use adequate-coverage WGS (AmpliconArchitect is designed for WGS, not panels/WES); apply FFPE-aware filtering; corroborate junctions across read-pair and split-read evidence.
| Pattern | Likely cause | Action |
|---|---|---|
| Depth caller: "amplification"; AA: ecDNA | Architecture only visible in the graph | Trust AA for architecture; depth gives amplitude only |
| AA ecDNA vs FISH negative | Subclonal ecDNA, or false-positive cycle | Check cell fraction; review graph balanced flow |
| AA "unknown" on a clear amplicon | Complex structure beyond short-read resolution | Escalate to optical mapping / long-read |
| BFB vs ecDNA ambiguous | Fold-back and circular signatures overlap | Inspect CN gradient (BFB) vs closed cycle (ecDNA) |
Operational rule: A depth caller establishes that a region is amplified and how much; it never establishes the architecture. An ecDNA call requires an AmpliconArchitect breakpoint graph with a closed cycle and an AmpliconClassifier ecDNA label, and ideally orthogonal confirmation (FISH, single-cell, optical mapping). Seeds must be vetted focal high-CN regions, not raw or arm-level calls.
| Threshold | Value | Source / Rationale |
|---|---|---|
| ecDNA prevalence | ~14% of cancers | Kim et al 2020; baseline expectation |
| CN seed threshold | CN >= ~4-5 focal | AmpliconSuite seeding; amplicons, not single-copy gains |
| Seed size | focal (sub-arm), not whole-arm | Arm-level seeds dilute focal amplicon signal |
| Assay | whole-genome sequencing | AmpliconArchitect needs genome-wide breakpoint coverage |
| Confirmation for ecDNA | graph cycle + classifier + orthogonal evidence | Depth alone is insufficient |
| Error / symptom | Cause | Solution |
|---|---|---|
| Amplicons at no known oncogene | Noisy or arm-level seeds | Seed vetted focal high-CN regions only |
| ecDNA "called" from a CNVkit profile | Depth-only claim, no graph | Run AmpliconArchitect + AmpliconClassifier |
| AA errors on contig names | Build mismatch | Match --ref and $AA_DATA_REPO to the BAM |
| AA fails to start | Missing Mosek license / data repo | Configure the academic Mosek license and $AA_DATA_REPO |
| Fragmented graph on a clear amplicon | Short-read limits / low coverage | Confirm with optical mapping or long reads |
| Classifier output all low-confidence | Coverage too low or FFPE artifacts | Use adequate-coverage WGS; FFPE-aware filtering |
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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。