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. 2015 Aug 19:8:359.
doi: 10.1186/s13104-015-1309-3.

Molgenis-impute: imputation pipeline in a box

Affiliations

Molgenis-impute: imputation pipeline in a box

Alexandros Kanterakis et al. BMC Res Notes. .

Abstract

Background: Genotype imputation is an important procedure in current genomic analysis such as genome-wide association studies, meta-analyses and fine mapping. Although high quality tools are available that perform the steps of this process, considerable effort and expertise is required to set up and run a best practice imputation pipeline, particularly for larger genotype datasets, where imputation has to scale out in parallel on computer clusters.

Results: Here we present MOLGENIS-impute, an 'imputation in a box' solution that seamlessly and transparently automates the set up and running of all the steps of the imputation process. These steps include genome build liftover (liftovering), genotype phasing with SHAPEIT2, quality control, sample and chromosomal chunking/merging, and imputation with IMPUTE2. MOLGENIS-impute builds on MOLGENIS-compute, a simple pipeline management platform for submission and monitoring of bioinformatics tasks in High Performance Computing (HPC) environments like local/cloud servers, clusters and grids. All the required tools, data and scripts are downloaded and installed in a single step. Researchers with diverse backgrounds and expertise have tested MOLGENIS-impute on different locations and imputed over 30,000 samples so far using the 1,000 Genomes Project and new Genome of the Netherlands data as the imputation reference. The tests have been performed on PBS/SGE clusters, cloud VMs and in a grid HPC environment.

Conclusions: MOLGENIS-impute gives priority to the ease of setting up, configuring and running an imputation. It has minimal dependencies and wraps the pipeline in a simple command line interface, without sacrificing flexibility to adapt or limiting the options of underlying imputation tools. It does not require knowledge of a workflow system or programming, and is targeted at researchers who just want to apply best practices in imputation via simple commands. It is built on the MOLGENIS compute workflow framework to enable customization with additional computational steps or it can be included in other bioinformatics pipelines. It is available as open source from: https://github.com/molgenis/molgenis-imputation.

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Figures

Fig. 1
Fig. 1
Outline of MOLGENIS-impute architecture. molgenis_impute.py is the python script with which the user interacts. The script can either install tools and reference panels or use MOLGENIS-compute to create and submit imputation scripts. The imputation BASH scripts and description of the pipeline are in a separate git repository.
Fig. 2
Fig. 2
MOLGENIS-impute’s workflow of three steps. Liftovering, phasing and imputation. Rectangles on the left contain a description of each step and on the right a respective demo python command.

References

    1. Marchini J, Howie B, Myers S, McVean G, Donnelly P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet. 2007;39(7):906–913. doi: 10.1038/ng2088. - DOI - PubMed
    1. Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet. 2009;5(6):e1000529. doi: 10.1371/journal.pgen.1000529. - DOI - PMC - PubMed
    1. Lu JT, Wang Y, Gibbs RA, Yu F. Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. Genome Biol. 2012;13(2):R15. doi: 10.1186/gb-2012-13-2-r15. - DOI - PMC - PubMed
    1. Holm H, Gudbjartsson DF, Sulem P, Masson G, Helgadottir HT, Zanon C, et al. A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nat Genet. 2011;43(4):316–320. doi: 10.1038/ng.781. - DOI - PMC - PubMed
    1. Browning BL, Browning SR. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am J Hum Genet. 2009;84(2):210–223. doi: 10.1016/j.ajhg.2009.01.005. - DOI - PMC - PubMed

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