The premise of this package is to generate primers for PCR/Sanger sequencing for either:
- a specific variant (hgvs_ variant nomenclature), either the whole exon or if not in an exon for the genomic position
- an exon (transcript number and exon )
- all exons of a transcript (transcript number)
- around a genomic position (chromosome and start/stop position)
This tool allows for primers based in hg19 or hg38.
The full documentation can be viewed here: add link to sphinx doc