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Analysis Methods | RNA Analysis | Splice Variant Calling

Splice Variant Calling

Splice variant calling is performed using the RNA Splice Variant Calling software. The inputs are BAM files and SJ.out.tab files from STAR. The outputs are VCF files which are the final output, and TSV of intergenic variants which are used in fusion merging.

For Research Use Only. Not for use in diagnostic procedures. 

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