Ensembl's VEP (Variant Effect Predictor) is popular for how it picks a single effect per gene as detailed here, its CLIA-compliant HGVS variant format, and Sequence Ontology nomenclature for variant effects.
Instead of the official instructions, we will use conda to install VEP and its dependencies. If you don't already have conda, install it into $HOME/miniconda3
as follows:
curl -sL https://repo.anaconda.com/miniconda/Miniconda3-py37_4.8.3-Linux-x86_64.sh -o /tmp/miniconda.sh
sh /tmp/miniconda.sh -bfp $HOME/miniconda3
Add the conda bin
folder into your $PATH
so that all installed tools are accessible via command-line. You can also add this to your ~/.bashrc
or ~/.profile
for this to persist across logins:
export PATH=$HOME/miniconda3/bin:$PATH
Download and install VEP, its dependencies, and also samtools/bcftools/liftOver:
conda install -qy -c conda-forge -c bioconda -c defaults ensembl-vep==100.3 samtools==1.9 bcftools==1.9 ucsc-liftover==377
Download VEP's offline cache for GRCh38, and the reference FASTA:
vep_install --AUTO cf --SPECIES homo_sapiens --ASSEMBLY GRCh38 --CACHEDIR $HOME/.vep
The command above is prone to networking issues. If it fails, manually download the GRCh38 cache and FASTA as follows:
rsync -av rsync://ftp.ensembl.org/pub/release-100/variation/indexed_vep_cache/homo_sapiens_vep_100_GRCh38.tar.gz $HOME/.vep
tar -zxf $HOME/.vep/homo_sapiens_vep_100_GRCh38.tar.gz -C $HOME/.vep
rsync -avr rsync://ftp.ensembl.org/pub/release-100/fasta/homo_sapiens/dna_index/ $HOME/.vep/homo_sapiens/100_GRCh38/
Test running VEP in offline mode on a GRCh38 VCF:
curl -sLO https://raw.githubusercontent.com/Ensembl/ensembl-vep/release/100/examples/homo_sapiens_GRCh38.vcf
vep --species homo_sapiens --assembly GRCh38 --offline --no_progress --no_stats --sift b --ccds --uniprot --hgvs --symbol --numbers --domains --gene_phenotype --canonical --protein --biotype --tsl --pubmed --variant_class --shift_hgvs 1 --check_existing --total_length --allele_number --no_escape --xref_refseq --failed 1 --vcf --minimal --flag_pick_allele --pick_order canonical,tsl,biotype,rank,ccds,length --dir $HOME/.vep --fasta $HOME/.vep/homo_sapiens/100_GRCh38/Homo_sapiens.GRCh38.dna.toplevel.fa.gz --input_file homo_sapiens_GRCh38.vcf --output_file homo_sapiens_GRCh38.vep.vcf --polyphen b --af --af_1kg --af_esp --regulatory