Reads the snvs_indels.tiers.tsv
(or v2's snv_indel_ann.tsv.gz
) file output
by PCGR.
Examples
x <- system.file(
"rawdata/test_data/umccrised/test_sample_WGS/small_variants",
"TEST-somatic.pcgr.snvs_indels.tiers.tsv",
package = "RNAsum"
)
(ptsv <- pcgr_tiers_tsv_read(x))
#> # A tibble: 99 × 61
#> CHROM POS REF ALT GENOMIC_CHANGE GENOME_VERSION VCF_SAMPLE_ID
#> <chr> <chr> <chr> <chr> <chr> <chr> <chr>
#> 1 3 179218303 G A 3:g.179218303G>A grch38 SBJ02999__PRJ22…
#> 2 17 7674894 G A 17:g.7674894G>A grch38 SBJ02999__PRJ22…
#> 3 13 110715614 C G 13:g.110715614C>G grch38 SBJ02999__PRJ22…
#> 4 13 110719444 G C 13:g.110719444G>C grch38 SBJ02999__PRJ22…
#> 5 8 20250093 C T 8:g.20250093C>T grch38 SBJ02999__PRJ22…
#> 6 8 13086457 C T 8:g.13086457C>T grch38 SBJ02999__PRJ22…
#> 7 10 31521795 G C 10:g.31521795G>C grch38 SBJ02999__PRJ22…
#> 8 9 132927250 G A 9:g.132927250G>A grch38 SBJ02999__PRJ22…
#> 9 3 47121452 G A 3:g.47121452G>A grch38 SBJ02999__PRJ22…
#> 10 6 117365075 G C 6:g.117365075G>C grch38 SBJ02999__PRJ22…
#> # ℹ 89 more rows
#> # ℹ 54 more variables: VARIANT_CLASS <chr>, SYMBOL <chr>, GENE_NAME <chr>,
#> # CCDS <chr>, CANONICAL <chr>, ENTREZ_ID <chr>, UNIPROT_ID <chr>,
#> # ENSEMBL_TRANSCRIPT_ID <chr>, ENSEMBL_GENE_ID <chr>, REFSEQ_MRNA <chr>,
#> # ONCOSCORE <chr>, ONCOGENE <chr>, TUMOR_SUPPRESSOR <chr>,
#> # ONCOGENE_EVIDENCE <chr>, TUMOR_SUPPRESSOR_EVIDENCE <chr>,
#> # DISGENET_CUI <chr>, DISGENET_TERMS <chr>, CONSEQUENCE <chr>, …