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Project description
Python pakcage for genomic variant analysis
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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