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Python pakcage for genomic variant analysis

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How to use?

pip install variant
  • run variant-effect in the command line
  • more functions will be supported in the future

variant-effect command can infer the effect of a mutation

 Usage: variant-effect [OPTIONS]

 Variant (genomic variant analysis in python)

╭─ Options ────────────────────────────────────────────────────────────────────────────────────────────────────────────╮
│ --input                 -i  TEXT       Input position file.                                                          │
│ --output                -o  TEXT       Output annotation file                                                        │
│ --reference             -r  TEXT       reference species                                                             │
│ --reference-gtf             TEXT       Customized reference gtf file.                                                │
│ --reference-transcript      TEXT       Customized reference transcript fasta file.                                   │
│ --reference-protein         TEXT       Customized reference protein fasta file.                                      │
│ --release               -e  INTEGER    ensembl release                                                               │
│ --type                  -t  [DNA|RNA]  (deprecated)                                                                  │
│ --strandness            -s             Use strand infomation or not?                                                 │
│ --pU-mode               -u             Make rRNA, tRNA, snoRNA into top priority.                                    │
│ --npad                  -n  INTEGER    Number of padding base to call motif.                                         │
│ --all-effects           -a             Output all effects.                                                           │
│ --with-header           -H             With header line in input file.                                               │
│ --columns               -c  TEXT       Sets columns for site info. (Chrom,Pos,Strand,Ref,Alt) [default: 1,2,3,4,5]   │
│ --help                  -h             Show this message and exit.                                                   │
╰──────────────────────────────────────────────────────────────────────────────────────────────────────────────────────╯

demo:

Store the following table in file (sites.tsv).

chr1 230703034 - C T
chr2 215361150 - A T
chr2 84906537 + C T
chr3 10301112 - G T
chr3 20301112 - G T
chr7 45893389 + G T
chr7 94669540 + G N
chr12 69353439 + A T
chr14 23645352 + G T

Run command variant-effect -i sites.tsv -r human -e 106 -t RNA to get the following output.

#chrom pos strand ref alt mut_type gene_name gene_pos transcript_name transcript_pos transcript_motif coding_pos codon_ref aa_pos aa_ref distance2splice
chr1 230703034 - G A ThreePrimeUTR ENSG00000135744(AGT) 42543 ENST00000680041(AGT-208) 1753 TGTGTCACCCCCAGTCTCCCA None None None None 295
chr2 215361150 - T A ThreePrimeUTR ENSG00000115414(FN1) 74924 ENST00000323926(FN1-201) 8012 GGCCCGCAATACTGTAGGAAC None None None None 476
chr2 84906537 + C T ThreePrimeUTR ENSG00000034510(TMSB10) 882 ENST00000233143(TMSB10-201) 327 CCTGGGCACTCCGCGCCGATG None None None None 148
chr3 10301112 - C A Silent ENSG00000157020(SEC13) 20001 ENST00000397117(SEC13-209) 1441 TTGATCATCTGCCTTAACGTG 849 CTG 283 L 35
chr3 20301112 - C A Intergenic None None None None None None None None None None
chr7 45893389 + G T ThreePrimeUTR ENSG00000146678(IGFBP1) 5030 ENST00000275525(IGFBP1-201) 1243 CAAAGCTCCTGCGTCTGTTTT None None None None 429
chr7 94669540 + G N ThreePrimeUTR ENSG00000242265(PEG10) 13216 ENST00000612941(PEG10-206) 6240 TTTTACCCCTGTCAGTAGCCC None None None None 5030
chr12 69353439 + A T ThreePrimeUTR ENSG00000090382(LYZ) 5059 ENST00000261267(LYZ-201) 695 TAGAACTAATACTGGTGAAAA None None None None 286
chr14 23645352 + G T ThreePrimeUTR ENSG00000100867(DHRS2) 15238 ENST00000344777(DHRS2-202) 1391 CTGCCATTCTGCCAGACTAGC None None None None 210

TODO:

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