SV and fusion transcript
Tabular data format for SV and fusion events
First line must be the header line, with following columns.
- gene_a
- gene on 5' end of a fusion. Do not apply value for intergenic break-end.
- isoform_a
- The RefSeq/Ensembl accession of gene_a. Leave blank for intergenic break-end.
- chr_a
- Chromosome name of gene_a. In case of intergenic translocation, use the 5' end of the break point. Use name "chr10" but not "10".
- position_a
- Chromosomal position of the 5' end break point, 0-based.
- strand_a
- + or -
- gene_b
- Gene on 3' end of a fusion. In case of intergenic translocation, leave unspecified.
- isoform_b
- The RefSeq/Ensembl accession of gene_b. Leave blank for intergenic break-end.
- chr_b
- Chromosome name of gene_b. In case of intergenic translocation, use the 3' end of the break point.
- position_b
- Chromosomal position of the 3' end break point, 0-based.
- strand_b
- + or -
Optional columns:
- Patient
- Sample
- Sampletype
Order of column doesn't matter.
Lines starting with "#" will be ignored.