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Imputation Server 2

Publication imputationserver2 nf-test follow on Twitter

This repository contains the Imputation Server 2 workflow to facilitate genotype imputation at scale. It serves as the underlying workflow of the Michigan Imputation Server.

Citation

Das S*, Forer L*, Schönherr S*, Sidore C, Locke AE, Kwong A, Vrieze S, Chew EY, Levy S, McGue M, Schlessinger D, Stambolian D, Loh PR, Iacono WG, Swaroop A, Scott LJ, Cucca F, Kronenberg F, Boehnke M, Abecasis GR, Fuchsberger C. Next-generation genotype imputation service and methods. Nature Genetics 48, 1284–1287 (2016). *Shared first authors

License

imputationserver2 is MIT Licensed and was developed at the Institute of Genetic Epidemiology, Medical University of Innsbruck, Austria.

Contact

If you have any questions about imputationserver2 please contact

If you encounter any problems, feel free to open an issue here.

Version History

Version 2.0.3 - Version 2.0.6 - Fix QC issues and remove HTSJDK index creation for input validation and QC.

Version 2.0.2 - Set minimac4 tmp directory (required for larger sample sizes).

Version 2.0.1 - Provide statistics to users in case QC failed; check normalized multiallelic variants in reference panel.

Version 2.0.0 - First stable release; migration of the imputation workflow to Nextflow.

Run with test data

The pipeline provides small test data to verify installation:

nextflow run main.nf -c conf/test_single_vcf.config

Run with custom configuration

job.config:

params {
    project                 = "my-test-project"
    build                   = "hg19"
    files                   = "tests/input/three/*.vcf.gz"
    allele_frequency_population              = "eur"
    mode                    = "imputation"
    refpanel_yaml           = "tests/hapmap-2/2.0.0/imputation-hapmap2.yaml"
    output                  = "output"
}

Run pipeline with job.config configuration:

nextflow run main.nf -c job.config

Parameters

Parameter Default Value Description
project null Project name
project_date date Project date
files null List of input files
allele_frequency_population null Allele Frequency Population information
refpanel_yaml null Reference panel YAML file
mode imputation Processing mode (e.g., 'imputation' or `qc-only``)
chunksize 20000000 Chunk size for processing
min_samples 20 Minimum number of samples needed
max_samples 50000 Maximum number of samples allowed
merge_samples true Execute compression and encryption workflow
password null Password for encryption
send_mail false Enable or disable email notifications
service.name Imputation Server 2 Service name
service.email null Service email
service.url null Service URL
user.name null User's name
user.email null User's email
phasing.engine eagle Phasing method (e.g., 'eagle' or beagle)
phasing.window 5000000 Phasing window size
imputation.enabled true Enable or disable imputation
imputation.window 500000 Imputation window size
imputation.minimac_min_ratio 0.00001 Minimac minimum ratio
imputation.min_r2 0 R2 filter value
imputation.meta false Enable or disable empirical output creation
imputation.md5 false Enable or disable md5 sum creation for results
imputation.create_index false Enable or disable index creation for imputed files
imputation.decay 0 Set minimac decay
encryption.enabled true Enable or disable encryption
encryption.aes false Enable or disable AES method for encryption
ancestry.enabled false Enable or disable ancestry analysis
ancestry.dim 10 Ancestry analysis dimension
ancestry.dim_high 20 High dimension for ancestry analysis
ancestry.batch_size 50 Batch size for ancestry analysis
ancestry.reference null Ancestry reference data
ancestry.max_pcs 8 Maximum principal components for ancestry
ancestry.k 10 K value for ancestry analysis
ancestry.threshold 0.75 Ancestry threshold

Reference Panel Configuration

This document describes the structure of a YAML file used to configure a reference panel for Imputation Servers. Reference panels are essential for genotype imputation, allowing the server to infer missing genotype data accurately.

YAML Structure

Field Description
name The name of the reference panel.
description A brief description of the reference panel.
version The version of the reference panel.
website The website where more information about the panel can be found.
category The category to which the reference panel belongs. TODO: has to be RefPanel
properties A section containing specific properties of the reference panel.

Properties

The properties section contains the following key-value pairs:

Property Description Required
id An identifier for the reference panel. yes
genotypes The location of the genotype files for the reference panel data. yes
sites The location of the site files for the reference panel data. yes
mapEagle The location of the genetic map file used for phasing with eagle. yes
refEagle The location of the BCF file for the reference panel data for eagle. yes
mapBeagle The location of the genetic map file used for phasing with Beagle. no
refBeagle The location of the BCF file for the reference panel data for Beagle. no
build The genome build version used for the reference panel (e.g., hg19 or hg38). yes
range Specify a range that is used for imputation (e.g. HLA) no
mapMinimac The location of the map file for Minimac no
populations A dictionary mapping population identifiers to their names. yes
qcFilter A dictionary mapping quality filters to their values. no
Populations

The populations section contains a dictionary mapping population identifiers to their names and sample size. This mapping helps categorize and label the populations represented in the reference panel.

Identifier Name
id The id of the popualtion (e.g. eur)
name The label of the population. (e.g. EUR)
samples Number of samples in the reference panel

Note: the population id has to be the same as in the legend files.

Quality Filters

Filter Name Default
overlap Minimal overlap between gwas data and reference panel 0.5
minSnps Minimal #SNPs per chunk 3
sampleCallrate Minimal sample call rate 0.5
mixedGenotypeschrX - 0.1
strandFlips Maximal allowed strand flips 100

Example YAML

Here's an example YAML configuration for a reference panel. This configuration describes a reference panel named "HapMap 2" for an Imputation Server, including details about its version, data sources, and populations represented. The files are stored on AWS S3 and are directly consumed by the pipeline from there.

name: HapMap 2
description: HapMap2 Reference Panel for Imputation Server
version: 2.0.0
website: http://imputationserver.sph.umich.edu
category: RefPanel

properties:
  id: hapmap2
  genotypes: s3://cloudgene/refpanels/hapmap/m3vcfs/hapmap_r22.chr$chr.CEU.hg19.recode.m3vcf.gz
  legend: s3://cloudgene/refpanels/hapmap/legends/hapmap_r22.chr$chr.CEU.hg19_impute.legend.gz
  mapEagle: s3://cloudgene/refpanels/hapmap/map/genetic_map_hg19_withX.txt.gz
  refEagle: s3://cloudgene/refpanels/hapmap/bcfs/hapmap_r22.chr$chr.CEU.hg19.recode.bcf
  build: hg19
  populations:
    - id: eur
      name: EUR
      samples: 60
    - id: off
      name: Off
      samples: -1

Note on $chr Variable

In the example YAML configuration provided, you may have noticed the presence of the $chr variable in some URLs. This variable is a placeholder for the chromosome number and will be replaced by the Nextflow pipeline.

Legend Files

A legend file is a tab-delimited file consisting of 5 columns (id, position, a0, a1, all.aaf).


Run with Cloudgene

Requirements:

  • Install Nextflow
  • Docker or Singularity
  • Java 14

Installation

  • Install cloudgene3: curl -s install.cloudgene.io
  • Download latest source code zip file from releases
  • Install impuationserver2 app: ./cloudgene install imputationserver2@latest
  • Install hapmap2 referenece panel: ./cloudgene install https://genepi.i-med.ac.at/downloads/imputation/imputation-hapmap2.zip
  • Start cloudgene server: ./cloudgene server
  • Open http://localhost:8082
  • Login with default admin account: username admin and password admin1978
  • Imputation can be tested with the following test file

Default Configuration

The default configuration runs with Docker and uses Nextflow's local executor.

Running on SLURM

Configure via web interface (Applications -> imputationserver -> Settings) or adapt/create file apps/imputationserver/nextflow.config and add the following:

process {
  executor = 'slurm'
  queue = 'QueueName'  // replace with your Queue name
}

errorStrategy = {task.exitStatus == 143 ? 'retry' : 'terminate'}
maxErrors = '-1'
maxRetries = 3

See more about SLURM Nextflow Documentation.

Running on AWS Batch

  1. Create AWS Batch queue and AMI role (see Nextflow Documentation)
  2. Configure via web interface (Applications -> imputationserver -> Settings) or adapt/create file apps/imputationserver/nextflow.config and add the following:
aws {
  region = 'eu-central-1'
  client {
    uploadChunkSize = 10485760
  }
  batch {
    cliPath = '/home/ec2-user/miniconda/bin/aws'
    executionRole = 'arn:aws:iam::***' // replace with your AMI role
  }
}

process {
  executor = 'awsbatch'
  queue = 'QueueName'  // replace with your Queue name
  scratch = false
}
  1. Got to Settings -> General and set Workspace to "S3" and enter the location of a subfolder in an S3 bucket. Enter the location of a subfolder in an S3 bucket. Currently, it must be a subfolder; a bucket won't work (Example: s3://cloudgene/workspace).

Optional add Wave and Fusion support to improve performance:

wave {
  enabled = true
  endpoint = 'https://wave.seqera.io'
}

fusion {
  enabled = true
}

Activate mail support

  • Configure mail server in Settings -> General -> Mail
  • Configure Nextflow to use Cloudgenes mail settings by add the following to the global configuration (Settings -> General -> Nextflow) or adapt/create files config/nextflow.confing (see Nextflow Documention for all available mail settings)
mail {
    smtp.host = "${CLOUDGENE_SMTP_HOST}"
    smtp.port = "${CLOUDGENE_SMTP_PORT}"
    smtp.user = "${CLOUDGENE_SMTP_USER}"
    smtp.password = "${CLOUDGENE_SMTP_PASSWORD}"
    smtp.auth = true
    smtp.starttls.enable = true
    smtp.ssl.protocols = 'TLSv1.2'
}
  • Add params.config.send_mail = true to the application specific configuration to activate mail notifications in the imputationserver2 pipeline

Adapt default parameters

Parameters can be changed in the `nextflow.config`` file of the application. Example:

params.chunk_size = 500000
params.imputation.window = 100000

Development

Build docker image locally

docker build -t genepi/imputationserver2:latest .

Run testcases

nf-test test