SnpEff

From UFRC
Revision as of 21:24, 6 December 2019 by Moskalenko (talk | contribs) (Text replacement - "#uppercase" to "uc")
Jump to navigation Jump to search

Description

snpeff website  

SnpEff
Genetic variant annotation and effect prediction toolbox. It annotates and predicts the effects of variants on genes (such as amino acid changes).
Features
  • Supports over 8,500 genomes.
  • Cancer variants analysis
  • GATK compatibile (-o gatk)
  • HGSV notations support (clinical)
SnpSift
SnpSift helps filtering and manipulating genomic annotated files (VCF). Once you annotated your files using SnpEff, you can use SnpSift to help you filter large genomic datasets in order to find the most significant variants

Required Modules

Serial

  • snpeff

System Variables

  • HPC_SNPEFF_DIR - main installation directory
  • HPC_SNPEFF_BIN - directory with executable scripts
  • HPC_SNPEFF_CONF - directory with the default configuration file.

Additional Information

In SnpEff-4.x series the upstream project provides a shell script 'snpEff', which can be used to run the program without calling java directly.

For snpeff/3.3h we provided a 'snpeff' wrapper that made running snpeff easier. For example,

java -Xmx2g -jar $HPC_SNPEFF_DIR/jar/snpEff.jar download -c $HPC_SNPEFF_CONF/snpEff.config -v athalianaTair10

could be run simply as

snpeff download -v athalianaTair10

To override the default 2g java memory setting use the following command on the command-line or in a job script:

export _JAVA_OPTIONS="-Xmx4g"

Reference Databases

Note: we provide a full mirror of snpeff/4.2 reference databases released by the upstream project, so please do not request addition of a new reference database unless you need a custom database built from your data. Please provide a fasta file and an annotation file for building the custom database.

See the installed database lists for



Citation

If you publish research that uses snpeff you have to cite it as follows:

SnpEff:

"A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.", Cingolani P, Platts A, Wang le L, Coon M, Nguyen T, Wang L, Land SJ, Lu X, Ruden DM. Fly (Austin). 2012 Apr-Jun;6(2):80-92. PMID: 22728672 [PubMed - in process]

SnpSift:

"Using Drosophila melanogaster as a model for genotoxic chemical mutational studies with a new program, SnpSift", Cingolani, P., et. al., Frontiers in Genetics, 3, 2012.