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This function identifies transcripts that cover specified junction breakpoints.

Usage

bp_junction_transcript_overlap(bp_junctions = NULL, ref_data = NULL)

Arguments

bp_junctions

A data frame with columns:

  • BP_CHROM: Chromosome of the breakpoint junction

  • BP_POSITION: Chromosome position of the breakpoint junction

ref_data

PCGR reference data bundle (list)

Value

A data frame with columns:

  • CHROM: Chromosome of the breakpoint junction

  • BP_POSITION: Position of the breakpoint junction

  • ENSEMBL_TRANSCRIPT_ID: Ensembl transcript ID covering the splice junction

  • ENSEMBL_GENE_ID: Ensembl gene ID

  • GENE_BIOTYPE: Biotype of the transcript

  • TRANSCRIPT_START: Start position of the transcript

  • TRANSCRIPT_END: End position of the transcript