本文へ移動
cccskills
無料GitHub で公開

alternative-splicing

Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.

インストール方法を見る

含まれるファイル(3)

  • SKILL.md4.2 KB
  • README.md446 B
  • references/technical_reference.md2.1 KB

SKILL.md(原文)

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。

Alternative Splicing

Version Compatibility

Reference examples assume recent stable releases of the preferred tools, especially splice-aware and the other tools listed below.

Before using code or command patterns, verify installed versions match the environment:

  • Python: python -c "import <module>; print(<module>.__version__)"
  • CLI: <tool> --version
  • If signatures differ, inspect the installed help or API and adapt the pattern instead of retrying unchanged.

Overview

Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.

When To Use This Skill

  • use when the task is differential splicing, isoform switching, or splice-aware QC
  • use when aligned RNA-seq reads and transcript annotations are available
  • use when the user needs event summaries, PSI-like metrics, or sashimi-style visualization

Quick Route

  • If the input is raw or minimally processed data, start with validation and QC before any modeling.
  • If the input is already processed, skip directly to the first workflow step that matches the user goal.
  • If the user asks for a biological conclusion, always produce at least one QC or confidence artifact alongside the final result.

Progressive Disclosure

  • Read references/technical_reference.md when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.
  • Keep SKILL.md as the main execution path and load the reference file only when the task or failure mode needs the extra detail.

Default Rules

  • Prefer Python-first workflows unless the task explicitly requires something else.
  • Keep intermediate and final outputs separated.
  • Record software versions, reference builds, and key parameters when they affect interpretation.
  • Favor reproducible tables and figures over one-off interactive-only outputs.

Expected Inputs

  • aligned RNA-seq reads
  • splice junction summaries
  • transcript annotation

Expected Outputs

  • event tables
  • isoform usage summaries
  • sashimi or splice plots

Preferred Tools

  • splice-aware quantification tools
  • pandas
  • matplotlib
  • genome track plotting utilities

Starter Pattern

Preferred starting point: splice-aware
Inputs: aligned RNA-seq reads, splice junction summaries, transcript annotation
Outputs: event tables, isoform usage summaries, sashimi or splice plots

Workflow

1. Confirm splice-aware inputs

Verify junction extraction, transcript annotation, and sample group definitions.

2. Choose analysis level

Use event-level methods for exon or junction usage and isoform-level methods for transcript switching.

3. Quantify splicing changes

Compute condition-specific splice usage and test for differential splicing.

4. Inspect representative loci

Plot junction-supported events to verify that statistical hits reflect visible changes.

5. Export interpretable results

Save event IDs, effect estimates, significance values, and plot-ready loci.

Output Artifacts

  • Recommended output layout:
    • results/ for final tables and serialized objects
    • figures/ for plots and static visual exports
    • qc/ for checks that justify downstream interpretation
  • Minimum expected outputs for this skill:
  • event tables
  • isoform usage summaries
  • sashimi or splice plots

Quality Review

  • Confirm identifiers and metadata join correctly before modeling or summarizing.
  • Generate at least one QC artifact before final biological interpretation.
  • Keep raw or minimally processed inputs separate from transformed outputs.
  • Check replicate structure, outlier samples, and whether counts versus normalized values are being mixed.
  • Export ranked or contrast-aware tables when downstream enrichment is likely.

Anti-Patterns

  • interpreting isoform changes without read support at informative junctions
  • mixing event- and transcript-level interpretations without stating which was used
  • skipping locus-level review of top hits

Related Skills

  • Bulk RNA Expression
  • RNA Quantification
  • Differential Expression
  • Small RNA Seq

Optional Supplements

  • pysam

レビュー

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。

同じリポジトリのスキル

概要と使いどころ

Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

alphafold

無料

Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

atac-seq

無料

ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

bindcraft

無料

End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

Guidance for choosing the right protein binder design tool. Use this skill when: (1) Deciding between BoltzGen, BindCraft, or RFdiffusion, (2) Planning a binder design campaign, (3) Understanding trade-offs between different approaches, (4) Selecting tools for specific target types. For specific tool parameters, use the individual tool skills (boltzgen, bindcraft, rfdiffusion, etc.).

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。

BioTender-max/awesome-bio-agent-skills2012026年7月2日 更新

BioTender-max のスキルをすべて見る

このスキルの問題を報告する