| name | star-ssse3 |
| description | Use when aligning RNA-seq reads to a reference genome or generating splice-aware genome indices for transcript alignment. |
| disable-model-invocation | true |
| user-invocable | true |
star-ssse3
Quick Start
- Command:
STAR-ssse3
- Local executable:
/home/vimalinx/miniforge3/envs/bio/bin/STAR-ssse3
- Full reference: See
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 STAR, BAM-input, or lift-over modes with the SSSE3-optimized STAR binary.
- Generate splice-junction-aware mappings for downstream counting, transcript assembly, or QC.
Common Patterns
STAR-ssse3 \
--runMode genomeGenerate \
--genomeDir star_index \
--genomeFastaFiles genome.fa \
--sjdbGTFfile genes.gtf \
--runThreadN 16
STAR-ssse3 \
--genomeDir star_index \
--readFilesIn sample_R1.fastq.gz sample_R2.fastq.gz \
--readFilesCommand zcat \
--runThreadN 16
STAR-ssse3 \
--genomeDir star_index \
--readFilesIn sample_R1.fastq.gz sample_R2.fastq.gz \
--readFilesCommand zcat \
--outSAMtype BAM SortedByCoordinate \
--runThreadN 16
Recommended Workflow
- Generate genome index using
--runMode genomeGenerate with --genomeDir, --genomeFastaFiles, and optional --sjdbGTFfile
- Align reads using
--runMode alignReads with --genomeDir pointing to the index and --readFilesIn specifying input files
- Set
--runThreadN to match available CPU cores for parallel processing
- Review alignment outputs (BAM) and splice junction files (SJ.out.tab) in the output directory
Guardrails
- Use genome indices generated with STAR version 2.7.4a or later; older indices are incompatible
- Provide uncompressed FASTA/FASTQ input files, or use
--readFilesCommand (e.g., zcat) for compressed files
- Specify
--genomeLoad NoSharedMemory unless you explicitly manage shared memory genome loading across runs