| name | starlong-sse3 |
| description | Use when aligning long RNA-seq reads to a reference genome using STARlong with SSE3 optimization, or when generating genome indices for long-read splice-aware alignment. |
| disable-model-invocation | true |
| user-invocable | true |
starlong-sse3
Quick Start
- Command:
STARlong-sse3
- Local executable:
/home/vimalinx/miniforge3/envs/bio/bin/STARlong-sse3
- Version: 2.7.11b
- Full reference: See references/help.md for complete options
When To Use This Tool
- Align long RNA-seq reads from PacBio or Nanopore with STARlong.
- Build or reuse STAR-compatible genome indices for long-read splice-aware mapping.
- Map full-length transcript reads while keeping STAR-style splice-junction outputs.
- Run a long-read-focused STAR wrapper using the SSE3-optimized binary.
Common Patterns
STARlong-sse3 \
--runMode genomeGenerate \
--genomeDir starlong_index \
--genomeFastaFiles genome.fa \
--sjdbGTFfile genes.gtf \
--runThreadN 16
STARlong-sse3 \
--genomeDir starlong_index \
--readFilesIn longreads.fastq \
--runThreadN 16
STARlong-sse3 \
--genomeDir starlong_index \
--readFilesIn longreads.fastq.gz \
--readFilesCommand zcat \
--outSAMtype BAM SortedByCoordinate \
--runThreadN 16
Recommended Workflow
- Prepare a genome directory and FASTA reference; optionally provide a GTF file with
--sjdbGTFfile for splice junction annotation.
- Generate the genome index with
--runMode genomeGenerate --genomeDir <dir> --genomeFastaFiles <fasta>.
- Align long reads with
--runMode alignReads --genomeDir <dir> --readFilesIn <reads.fq>.
- Verify output files (alignments and splice junctions) and review summary statistics before downstream analysis.
Guardrails
- Always specify
--genomeDir pointing to a valid STAR genome index directory.
- Use
--runThreadN to match available CPU cores; avoid oversubscribing system resources.
- For long reads, ensure the genome index was built with appropriate
--genomeSAindexNbases scaled to genome size.