| name | star-avx |
| description | Use when aligning RNA-seq reads to a reference genome with splice-aware mapping, generating genome indices, or processing single-cell RNA-seq data with STARsolo. |
| disable-model-invocation | true |
| user-invocable | true |
star-avx
Quick Start
- Command:
STAR-avx [options] --genomeDir /path/to/genome/index/ --readFilesIn R1.fq R2.fq
- Local executable:
/home/vimalinx/miniforge3/envs/bio/bin/STAR-avx
- Full reference:
references/help.md
When To Use This Tool
- Build STAR genome indices for RNA-seq alignment.
- Perform splice-aware alignment of short RNA-seq reads against a genome.
- Run STARsolo, BAM-input, or lift-over modes with the AVX-optimized STAR binary.
- Generate splice-junction-aware mappings for downstream counting, transcript assembly, or QC.
Common Patterns
STAR-avx \
--runMode genomeGenerate \
--genomeDir star_index \
--genomeFastaFiles genome.fa \
--sjdbGTFfile genes.gtf \
--runThreadN 16
STAR-avx \
--genomeDir star_index \
--readFilesIn sample_R1.fastq.gz sample_R2.fastq.gz \
--readFilesCommand zcat \
--runThreadN 16
STAR-avx \
--genomeDir star_index \
--readFilesIn sample_R1.fastq.gz sample_R2.fastq.gz \
--readFilesCommand zcat \
--outSAMtype BAM SortedByCoordinate \
--runThreadN 16
Recommended Workflow
- Generate a genome index using
--runMode genomeGenerate with --genomeFastaFiles and --sjdbGTFfile
- Align reads with
--runMode alignReads specifying --genomeDir and --readFilesIn
- Set appropriate thread count with
--runThreadN based on available cores
- Review output alignments (SAM/BAM) and splice junction files (
SJ.out.tab)
Guardrails
- Genome index must be compatible with STAR version 2.7.4a or later (
versionGenome parameter)
- Ensure
--genomeSAindexNbases is scaled appropriately for small genomes: min(14, log2(GenomeLength)/2 - 1)
- Use
--readFilesCommand zcat for compressed .gz input files; FASTA/FASTQ inputs cannot be zipped directly