Export target info metadata
pmo_export_target_info_meta_table.RdPrimer sequences and primer/insert genomic locations are flattened into
forward_primer_*, reverse_primer_*, and insert_* columns.
Examples
p <- read_pmo(
system.file("extdata", "example_full_pmo.json.gz", package = "pmotoolsr"))
head(pmo_export_target_info_meta_table(p))
#> # A tibble: 6 × 21
#> target_name forward_primer_seq reverse_primer_seq forward_primer_chrom
#> <chr> <chr> <chr> <chr>
#> 1 t96 TTTTTCTCCACTTTGTAATTTTTAT… CGGGTGGTATCATGAGA… Pf3D7_14_v3
#> 2 t95 ACACTTCAACTACACTTTTTAATTT… AGATCTTATGTTAAACT… Pf3D7_14_v3
#> 3 t94 AAAATCTTTTGGTATTGTATTTTGA… AAACGGAATCACTTATG… Pf3D7_14_v3
#> 4 t50 TGTAAAAGGAAAATGTCTTACGTGG… ATTCAAAACCAATAGTA… Pf3D7_08_v3
#> 5 t36 GGAATATTTGTGATTTAGGATGTAA… CAAATATATCTCTTCGC… Pf3D7_05_v3
#> 6 t88 ATTTACATGATGTAACTGAATCTCA… AGCCAGTATTCTTTTTA… Pf3D7_13_v3
#> # ℹ 17 more variables: forward_primer_end <int>,
#> # forward_primer_genome_id <dbl>, forward_primer_start <int>,
#> # forward_primer_strand <chr>, gene_name <chr>, insert_chrom <chr>,
#> # insert_end <int>, insert_genome_id <dbl>, insert_ref_seq <chr>,
#> # insert_start <int>, insert_strand <chr>, reverse_primer_chrom <chr>,
#> # reverse_primer_end <int>, reverse_primer_genome_id <dbl>,
#> # reverse_primer_start <int>, reverse_primer_strand <chr>, …