Creates a plot that visualizes the selected gene and optionally marks variant positions.
1 |
gff_file |
Data frame including columns "seqid", "start", "end", "type" and "ID". |
gene_name |
ID of the gene of interest. Should be the same for the GFF and VCF input. |
vcf_file |
Data frame including columns "POS", "ANN....GENEID", "ANN....EFFECT" and optionally "Genotype". SnpSift-filtered VCF file. |
plot_title |
Customize plot title. Default is set to input of gene_name. |
facets |
Split plot into facets. Set to 'variants' or 'genotype' (this requires column "Genotype"). |
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