Agent skill · Data & Analytics

bio-small-rna-seq-mirdeep2-analysis

Discover novel miRNAs and quantify known miRNAs using miRDeep2 de novo prediction from small RNA-seq data. Use when identifying new miRNAs or performing comprehensive miRNA profiling with discovery.

majiayu000github.com/majiayu000GitHub ↗
claude-codeMIT
Install
npx skills add majiayu000/claude-skill-registry --skill mirdeep2-analysis --agent claude-code

Same command for any agent — swap --agent for codex, cursor, copilot.

Facts
Files in the skill folder: 2
SKILL.md size: 4 KB
Bundled scripts: none
Path: skills/analysis/mirdeep2-analysis/SKILL.md
Open the folder on GitHub →
Where it comes from
Stars: 534
Language: HTML

Weekly change comes from our own snapshots, not the repository page — it measures attention, not adoption.

From the SKILL.md

# miRDeep2 Analysis ## Workflow Overview ``` Collapsed reads (FASTA) | v mapper.pl ---------> Align to genome, create ARF file | v miRDeep2.pl -------> Predict novel miRNAs, quantify known | v quantifier.pl -----> Quantify known miRNAs only (optional) ``` ## Step 1: Prepare Genome Index ```bash # Build bowtie index for miRDeep2 mapper bowtie-build genome.fa genome_index ``` ## Step 2: Map Reads with mapper.pl ```bash # Collapse reads and map to genome mapper.pl reads.fastq \ -e \ -h \ -i \ -j \ -k TGGAATTCTCGGGTGCCAAGG \ -l 18 \ -m \ -p genome_index \ -s reads_collapsed.fa \ -t reads_vs_genome.arf \ -v # Key options: # -e: Input is FASTQ # -h: Parse Illumina headers # -k: Clip 3' adapter # -l 18: Discard reads < 18 nt # -m: Collapse reads # -p: Bowtie index prefix # -s: Output collapsed FASTA # -t: Output ARF alignment file ``` ## Step 3: Run miRDeep2 Prediction ```bash # Predict novel miRNAs miRDeep2.pl \ reads_collapsed.fa \ genome.fa \ reads_vs_genome.arf \ mature_ref.fa \ mature_other.fa \ hairpin_ref.fa \ -t Human \ 2> report.log # Arguments: # 1. Collapsed reads FASTA # 2. Genome FASTA # 3. Alignment ARF file # 4. Known mature miRNAs (same species) # 5. Known mature miRNAs (o

What's inside
Steps it walks through
  1. Workflow Overview
  2. Step 1: Prepare Genome Index
  3. Step 2: Map Reads with mapper.pl
  4. Step 3: Run miRDeep2 Prediction
  5. Prepare miRBase References
  6. Step 4: Quantify Known miRNAs Only
  7. Output Files
  8. Interpret miRDeep2 Scores
  9. Parse Results in Python
  10. Related Skills
Ships with 1 file
  • metadata.json
Commands it runs
Build bowtie index for miRDeep2 mapper
bowtie-build genome.fa genome_index
Collapse reads and map to genome
mapper.pl reads.fastq \
Key options:
Predict novel miRNAs
miRDeep2.pl \
reads_collapsed.fa \
genome.fa \
reads_vs_genome.arf \
More from claude-skill-registry
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About this skill
What does the bio-small-rna-seq-mirdeep2-analysis skill do?

Discover novel miRNAs and quantify known miRNAs using miRDeep2 de novo prediction from small RNA-seq data. Use when identifying new miRNAs or performing comprehensive miRNA profiling with discovery.

How do I install it?

Run `npx skills add majiayu000/claude-skill-registry --skill mirdeep2-analysis --agent claude-code` — it drops the skill into your project so the agent can pick it up. Swap the --agent value for codex, cursor or copilot if you use one of those.

Where does this skill come from?

From majiayu000/claude-skill-registry, a repository with 534 stars. We read it straight from the repository tree rather than a submitted listing, so what you see here is what is actually published.

Is a popular skill a good skill?

Not necessarily. Stars measure attention, not adoption — a repository can trend for a week and be abandoned. That is why we show the weekly change from our own snapshots next to the total, instead of a single flattering number.

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