bio-read-alignment-star-alignment — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-read-alignment-star-alignment (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Reference examples tested with: STAR 2.7.11+, Subread 2.0+, fastp 0.23+, kallisto 0.50+
Before using code patterns, verify installed versions match. If versions differ:
<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Align RNA-seq reads with STAR" → Map RNA-seq reads to a reference genome with fast, sensitive splice-aware alignment. Preferred for large datasets and downstream fusion/chimeric read detection.
STAR --runMode alignReads --genomeDir index/ --readFilesIn R1.fq R2.fq --outSAMtype BAM SortedByCoordinate# Basic index generation
STAR --runMode genomeGenerate \
--runThreadN 8 \
--genomeDir star_index/ \
--genomeFastaFiles reference.fa \
--sjdbGTFfile annotation.gtf \
--sjdbOverhang 100 # Read length - 1# For 150bp reads, use sjdbOverhang=149
STAR --runMode genomeGenerate \
--runThreadN 8 \
--genomeDir star_index_150/ \
--genomeFastaFiles reference.fa \
--sjdbGTFfile annotation.gtf \
--sjdbOverhang 149# Paired-end alignment
STAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn reads_1.fq.gz reads_2.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinateSTAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn reads.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinate# Two-pass mode for better novel junction detection
STAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn r1.fq.gz r2.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinate \
--twopassMode Basic# Output gene counts (like featureCounts)
STAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn r1.fq.gz r2.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinate \
--quantMode GeneCountsOutput: sample_ReadsPerGene.out.tab with columns:
# ENCODE recommended settings
STAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn r1.fq.gz r2.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinate \
--outSAMunmapped Within \
--outSAMattributes NH HI AS NM MD \
--outFilterType BySJout \
--outFilterMultimapNmax 20 \
--outFilterMismatchNmax 999 \
--outFilterMismatchNoverReadLmax 0.04 \
--alignIntronMin 20 \
--alignIntronMax 1000000 \
--alignMatesGapMax 1000000 \
--alignSJoverhangMin 8 \
--alignSJDBoverhangMin 1# For chimeric/fusion detection
STAR --runThreadN 8 \
--genomeDir star_index/ \
--readFilesIn r1.fq.gz r2.fq.gz \
--readFilesCommand zcat \
--outFileNamePrefix sample_ \
--outSAMtype BAM SortedByCoordinate \
--chimSegmentMin 12 \
--chimJunctionOverhangMin 8 \
--chimOutType Junctions WithinBAM SoftClip \
--chimMainSegmentMultNmax 1| File | Description |
|---|---|
| *Aligned.sortedByCoord.out.bam | Sorted BAM file |
| *Log.final.out | Alignment summary statistics |
| *Log.out | Detailed log |
| *SJ.out.tab | Splice junctions |
| *ReadsPerGene.out.tab | Gene counts (if --quantMode) |
| *Chimeric.out.junction | Fusion candidates (if chimeric) |
# Reduce memory for limited systems
STAR --genomeLoad NoSharedMemory \
--limitBAMsortRAM 10000000000 \ # 10GB for sorting
...
# For very large genomes, limit during index generation
STAR --runMode genomeGenerate \
--limitGenomeGenerateRAM 31000000000 \ # 31GB
...# Load genome into shared memory (for multiple samples)
STAR --genomeLoad LoadAndExit --genomeDir star_index/
# Run alignments (faster startup)
STAR --genomeLoad LoadAndKeep --genomeDir star_index/ ...
# Remove from memory when done
STAR --genomeLoad Remove --genomeDir star_index/| Parameter | Default | Description |
|---|---|---|
| --runThreadN | 1 | Number of threads |
| --sjdbOverhang | 100 | Read length - 1 |
| --outFilterMultimapNmax | 10 | Max multi-mapping |
| --alignIntronMax | 0 | Max intron size |
| --outFilterMismatchNmax | 10 | Max mismatches |
| --outSAMtype | SAM | Output format |
| --quantMode | - | GeneCounts for counting |
| --twopassMode | None | Basic for two-pass |
~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.