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Minimac4 is a latest version in the series of genotype imputation software - preceded by Minimac3 (2015), Minimac2 (2014), minimac (2012) and MaCH (2010). Minimac4 is a lower memory and more computationally efficient implementation of the original algorithms with comparable imputation quality.

The Minimac3 mailing list has been renamed as the Minimac4 mailing list. If you were already a member, no need to re-join. If not, please join our mailing list to get updates about future releases or report possible bugs or email them to Sayantan Das.


Minimac4 (version 1.0.2, updated 6.29.2017) is currently available for testing purposes only (while we still run more tests and wait on feedback about potential bugs). Commonly used reference panels in M3VCF format are available for download in Reference Panels.

Github Repo: : Minimac4 Github

What's New

The input file format, output file formats and typical command lines are same in Minimac4 (as they were in minimac3). Some of the main new features are summarized below:

  • Improved Speed - Minimac4 is approximately 6 times faster for 1000 Genomes Phase 1 and Phase 3 and 2 times faster for the HRC reference panels at comparable accuracy (details of accuracy for imputing into 10 European samples are given here). The speed can be further improved by tuning the approximation parameters (see below), but we recommend using the default values.
  • Automated Chunking - Minimac4 automatically chunks the whole chromosome (into overlapping chunks), analyzes each chunk sequentially and then concatenates the imputed chunks back. This caps the memory usage across different chromosomes (memory requirement is based on chunk size, not chromosome size). The length of the chunk and the overlap can be controlled by the --chunkLengthMb and --chunkLengthOverlapMb options, although we recommend using the default values of 20 and 3, respectively.
  • Approximations - Minimac4 uses some simple approximations to speed up the imputation analyses. The levels of approximation can be controlled by the parameters --probThreshold, --diffThreshold, and --topThreshold (details given in Minimac4 Usage). Higher levels of approximation will reduce the compute time but marginally reduce the imputation accuracy. We recommend using the default values (0.01).
  • Improved Chromosome X/Y Support - Minimac4 can handle different ploidys in the same VCF file for imputation of sex chromosomes. For example, for the non-PAR region on chromosome X, males and females can be imputed together, irrespective of whether males are coded as haploids or diploids. However, each sample must have a fixed ploidy. Thus, PAR and non-PAR regions still need to be imputed separately. Please see Chromosome X Imputation for more details.
  • Other Helpful Features
    • We introduced a new feature called --memUsage that will estimate and report the memory required by Minimac4. This feature should be useful for users running their jobs on a compute cluster that requires memory specification.
    • We introduced some other FORMAT options for the output dosage data, allowing users to retrieve haplotype dosages, genotype probabilities, genotype dosages or any other measure of summary that they want.
    • We have fixed the bug related to FILTER=GENOTYPED and FILTER=GENOTYPED_ONLY which was causing a crash in bcftools.
  • Obsolete Features
    • In Minimac4, we removed the --doseOutput and --hapOutput options. Please use DosageConvertor to convert your files to MaCH or PLINK dosage format.
    • Currently Minimac4 can ONLY handle M3VCF format files. If your reference panel is in VCF format, please use Minimac3 to convert the VCF file to M3VCF (along with parameter estimation) and then use that M3VCF for imputation using Minimac4. The same holds for the option --processReference as well. Although the handle is made available, we will implement it in a later version.
    • Parameters such as --rounds, --states, --rec, --err have been deactivated for now until we implement parameter estimation in minimac4.

Reference Panels for Download

Some commonly used reference panels are available for download here:

Reference Panel Number
of Samples
File Format Parameter
Chromosomes Link
1000 Genomes

Phase 3
(version 5)

2,504 VCF - 1-22,X Download
M3VCF YES 1-22,X Download
NO 1-22,X Download
VCF,M3VCF YES X Download
1000 Genomes

Phase 1
(version 3)

1,092 VCF - 1-22,X Download
M3VCF YES 1-22,X Download
NO 1-22,X Download
VCF,M3VCF YES X Download