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A tool for calculating imputation accuracy by comparing imputation results to WGS data.

Documentation and scripts provided for calculating imputation accuracy. Tested using Minimac4, Beagle, Impute5 and our deep learning based imputation tool project (in progress). Should work with any imputed VCF file that has GT or GT+DS format fields.

Requirements

  • samtools/bcftools: used to calculate MAFs
  • python v3: source code was implemented and tested on python 3.6
    • pandas
    • numpy
    • cyvcf2

Required command line arguments are:

The following inputs, in vcf.gz format, including its respective tabix tbi file, are required to run.

  • ga: genotype array file used as input for imputation
  • imputed: imputation results
  • wgs: ground truth file, containing experimentally determined genotypes (i.e. Whole Genome Sequencing data)

IMPORTANT PREREQUISITE: All files provided must be in vcf.gz format (compressed, tabixed). Alleles must match, in other words: NO SWAPS, NO FLIPS, SAME BUILD!!! It is not necessary to provide allele frequencies, since the tool will calculate it internally using bcftools.

Usage:

The help shows all the required arguments listed above, plus optional arguments.

python3 Compare_imputation_to_WGS.py -h
usage: Compare_imputation_to_WGS.py --ga <input_genotype_array.vcf.gz> --imputed <imputed_file.vcf.gz> --wgs <whole_genome_file.vcf.gz>
Use -h or --help to display help.

arguments:
  -h, --help            show this help message and exit
  --ga GA               optional, path to genotype array file in vcf.gz format, with tbi
  --wgs WGS             required, path to whole genome file in vcf.gz format, with tbi
  --imputed IMPUTED     required, path to imputed file in vcf.gz format, with tbi
  --ref REF             optional, path to reference panel file in vcf.gz
                        format, with tbi. Used for MAF calculation. WGS file
                        will be used if no reference file is provided.
  --max_total_rows MAX_TOTAL_ROWS
                        optional, maximun number of rows or variants to be loaded
                        simultaneously, summing all chunks loaded by all cores
  --max_per_core MAX_PER_CORE
                        optional, maximun number of variants per chunk per core, lower
                        it to avoid RAM overload
  --min_per_core MIN_PER_CORE
                        optional, minimun number of variants per chunk per core,
                        increase to avoid interprocess communication overload
  --sout SOUT           optional, output file path/name per sample, default is
                        the same as the imputed file with
                        _per_sample_results.txt suffix
  --vout VOUT           optional, output file path/name per variant, default is
                        the same as the imputed file with
                        _per_variant_results.txt suffix

A detailed report with accuracy ratio, F1 score, Pearson correlation (r2) is generated and wrote to the output file (i.e accuracy_result.txt)

How to run example:

python3.6 Compare_imputation_to_WGS.py --ga aric_GT_ancestry-5_cad_190625.vcf.chr1.gz --imputed aric_intersectWGS_rpt-1_ancestry-5_phasing-eagle_seed-E_imputed-HRC_cad_190625.vcf.chr1.gz --wgs aric_WGS_ancestry-5_cad_190625.recode.vcf.chr1.gz

Results:

Processing  239 imputed samples
Processing chunk: 1 Max rows per chunk: 10000
1 Read imputed file time:  0.0004201233386993408
2 Chunking time:  8.239876478910446e-06
3 Calculation time:  0.16841873712837696
4 Merging calculations per sample time:  0.0037479093298316
Results per sample at: aric_intersectWGS_rpt-1_ancestry-5_phasing-eagle_seed-E_imputed-HRC_cad_190625.vcf.chr1_per_sample_results.txt
Results per variant at: aric_intersectWGS_rpt-1_ancestry-5_phasing-eagle_seed-E_imputed-HRC_cad_190625.vcf.chr1_per_variant_results.txt
Total run time (sec): 0.17389075085520744

The results will be displayed as the example bellow (per variant):

position        SNP     REF_MAF IMPUTED_MAF     WGS_MAF F-score concordance_P0  IQS     r2      precision       recall  TP      TN      FP      FN TP_ratio TN_ratio        FP_ratio        FN_ratio        RMSE
22:48742072     22:48742072_G_A 0.0003  0.0013  0.0093  0.992   0.984   0.246   0.143   1.0     0.984   754     738     0       12      1.0     0.984       0.0     0.016   0.126
22:48742498     22:48742498_G_A 0.0028  0.0     0.002   0.998   0.996   0.0     0.014   1.0     0.996   752     749     0       3       1.0     0.996       0.0     0.004   0.063
22:48743012     22:48743012_C_A 0.061   0.0578  0.0665  0.947   0.882   0.479   0.3     0.946   0.948   804     610     46      44      0.946   0.933       0.054   0.067   0.307
22:48742525     22:48742525_G_A 0.0041  0.0013  0.0033  0.998   0.996   0.57    0.36    1.0     0.996   754     747     0       3       1.0     0.996       0.0     0.004   0.066
22:48741511     22:48741511_C_T 0.0009  0.0007  0.0007  1.0     1.0     1.0     0.999   1.0     1.0     753     751     0       0       1.0     1.00.0      0.0     0.002
22:48741402     22:48741402_A_G 0.2096  0.0439  0.2646  0.836   0.621   0.233   0.185   0.879   0.796   814     370     112     208     0.879   0.640.121   0.36    0.591
22:48742178     22:48742178_G_A 0.0089  0.0007  0.0153  0.986   0.971   0.081   0.062   1.0     0.972   753     729     0       22      1.0     0.971       0.0     0.029   0.167
22:48741385     22:48741385_T_C 0.3718  0.113   0.4149  0.863   0.547   0.192   0.168   0.768   0.984   1078    83      325     18      0.768   0.822       0.232   0.178   0.656
22:48741702     22:48741702_C_T 0.001   0.0047  0.0293  0.976   0.956   0.287   0.165   0.995   0.958   755     712     4       33      0.995   0.956       0.005   0.044   0.238

Results per sample:

imputed_ids     WGS_ids F-score concordance_P0  r2      precision       recall  TP      TN      FP      FN      TP_ratio        TN_ratio        FP_ratio    FN_ratio        RMSE
A00003_A00003   A00003_A00003   0.976   0.95    0.497   0.972   0.981   103.0   94.0    3.0     2.0     0.972   0.979   0.028   0.021   0.152
A00018_A00018   A00018_A00018   0.932   0.851   0.696   0.972   0.896   103.0   84.0    3.0     12.0    0.972   0.875   0.028   0.125   0.296
A00056_A00056   A00056_A00056   0.99    0.98    0.613   0.981   1.0     104.0   96.0    2.0     0.0     0.981   1.0     0.019   0.0     0.162
A00080_A00080   A00080_A00080   0.986   0.97    0.671   0.981   0.991   106.0   93.0    2.0     1.0     0.981   0.989   0.019   0.011   0.141
A00083_A00083   A00083_A00083   0.99    0.98    0.56    0.981   1.0     104.0   96.0    2.0     0.0     0.981   1.0     0.019   0.0     0.128
A00099_A00099   A00099_A00099   0.99    0.98    0.139   0.99    0.99    102.0   98.0    1.0     1.0     0.99    0.99    0.01    0.01    0.138
A00120_A00120   A00120_A00120   0.976   0.96    0.5     0.962   0.99    101.0   96.0    4.0     1.0     0.962   0.99    0.038   0.01    0.21
A00146_A00146   A00146_A00146   0.972   0.941   0.64    0.963   0.981   103.0   93.0    4.0     2.0     0.963   0.979   0.037   0.021   0.176
A00152_A00152   A00152_A00152   0.986   0.97    0.403   0.981   0.99    103.0   96.0    2.0     1.0     0.981   0.99    0.019   0.01    0.17

The results can be interpreted as follows.

Metrics per variant:

  • REF_MAF: Reference Panel MAF (if reference panel is provided)
  • IMPUTED_MAF: Imputed MAF
  • WGS_MAF: Whole Genome MAF
  • F-score: macro F-score (not weighted),
  • concordance_P0: accuracy ratio (concordance, from the article cited bellow [1]),
  • IQS: imputation quality score (from the same article [1])
  • precision: precision
  • recall: recall
  • TP: true positives
  • TN: true negatives
  • FP: false positives
  • FN: false negatives
  • TP_ratio: true positives ratio
  • TN_ratio: true negatives ratio
  • FP_ratio: false positives ratio
  • FN_ratio: false negatives ratio
  • RMSE: root mean squared error

Metrics per sample:

  • F-core: F-score per sample
  • concordance_P0: accuracy ratio
  • r2: r-squared
  • precision: precision
  • recall: recall
  • TP: true positives
  • TN: true negatives
  • FP: false positives
  • FN: false negatives
  • TP_ratio: true positives ratio
  • TN_ratio: true negatives ratio
  • FP_ratio: false positives ratio
  • FN_ratio: false negatives ratio
  • RMSE: root mean squared error

Check sample_data folder for real sample of inputs/outputs data and test run:

cd sample_data
python3 ../Compare_imputation_to_WGS.py --ga input_genotype_array_100samples.vcf.gz --wgs whole_genome_file_100samples.vcf.gz --imputed imputed_file_100samples.vcf.gz

This message will show up if everything worked:

Processing chunk: 1 Max rows per chunk: 10000
...
Processing chunk: 52 Max rows per chunk: 10000
1 Read imputed file time:  5.211546601727605
2 Chunking time:  0.0284710843116045
3 Calculation time:  90.96355835348368
4 Merging calculations per sample time:  20.620813813060522
Results per sample at: imputed_file_100samples.vcf_per_sample_results.txt
Results per variant at: imputed_file_100samples.vcf_per_variant_results.txt
Total run time (sec): 117.97938374243677

After running this example, you can visualize the results for the test sample data in:

  • imputed_file_100samples.vcf_per_sample_results.txt
  • imputed_file_100samples.vcf_per_variant_results.txt

For example:

head imputed_file_100samples.vcf_per_variant_results.txt

position        SNP     IMPUTED_MAF     WGS_MAF F-score concordance_P0  IQS     r2      precision       recall  TP      TN      FP      FN TP_ratio TN_ratio        FP_ratio        FN_ratio        RMSE
22:16050783     22:16050783_A_G 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.001
22:16050922     22:16050922_T_G 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0
22:16050984     22:16050984_C_G 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0
22:16051269     22:16051269_G_T 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0
22:16051477     22:16051477_C_A 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.006
22:16052240     22:16052240_C_G 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0
22:16052271     22:16052271_G_A 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.001
22:16052428     22:16052428_G_A 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0
22:16052639     22:16052639_C_T 0.0     0.0     1.0     1.0     0.0     0.0     1.0     1.0     100     100     0       0       1.0     1.00.0      0.0     0.0

References:

[1] Ramnarine S, Zhang J, Chen LS, Culverhouse R, Duan W, Hancock DB, Hartz SM, Johnson EO, Olfson E, Schwantes-An TH, Saccone NL. When does choice of accuracy measure alter imputation accuracy assessments?. PloS one. 2015 Oct 12;10(10):e0137601.

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