Downloading: s3://natera-platform-sandbox/pipeline-resources/ngi-igenomes/igenomes/Homo_sapiens/GATK/GRCh38/Sequence/WholeGenomeFasta/Homo_sapiens_assembly38.fasta
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/3a/ebd77ff94943a923a526f0e82b1717/.command.sh
  Downloading: s3://natera-platform-sandbox/pipeline-inputs/test_sarek/end_to_end_regression/output_runs/dev_latest_regression_eks__47a821d--20260221-174447/preprocessing/recalibrated/HCC1395_tumor/HCC1395_tumor.recal.bam.bai
  Downloading: s3://natera-platform-sandbox/pipeline-resources/ngi-igenomes/igenomes/Homo_sapiens/GATK/GRCh38/Sequence/WholeGenomeFasta/Homo_sapiens_assembly38.fasta.fai
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/36/98a3de0f09a2e45b677197ed1b71bf/HCC1395_tumor_vs_HCC1395_BL.snv_indel.merged.vcf.gz
  Downloading: s3://natera-platform-sandbox/pipeline-inputs/test_sarek/end_to_end_regression/output_runs/dev_latest_regression_eks__47a821d--20260221-174447/preprocessing/recalibrated/HCC1395_tumor/HCC1395_tumor.recal.bam
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/36/98a3de0f09a2e45b677197ed1b71bf/HCC1395_tumor_vs_HCC1395_BL.snv_indel.merged.vcf.gz.tbi
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/3a/ebd77ff94943a923a526f0e82b1717/.command.run
==> STAGING COMPLETE (8 inputs)

This is WhatsHap 2.8 running under Python 3.9.23
[W::hts_idx_load3] The index file is older than the data file: HCC1395_tumor.recal.bam.bai
[W::hts_idx_load3] The index file is older than the data file: HCC1395_tumor.recal.bam.bai
[E::idx_find_and_load] Could not retrieve index file for 'input_filtered.vcf.gz'
[E::idx_find_and_load] Could not retrieve index file for 'input_filtered.vcf.gz'
[E::idx_find_and_load] Could not retrieve index file for 'input_filtered.vcf.gz'
Working on 2 samples from 2 families
WARNING: Skipping duplicated position 10454230 on chromosome 'chr21' Hiding further warnings of this type, use --debug to show

# Working on contig chr21 in individual HCC1395_BL
Found 8 usable heterozygous variants (0 skipped due to missing genotypes)
WARNING: Sample 'HCC1395_BL' not found in any BAM/CRAM file.
Found 0 reads covering 0 variants
Kept 0 reads that cover at least two variants each
Selected 0 most phase-informative reads covering 0 variants
Best-case phasing would result in 0 non-singleton phased blocks (0 singletons). 
Phasing 1 sample by solving the MEC problem ...
No. of phased blocks: 0

# Working on contig chr21 in individual HCC1395_tumor
Found 197 usable heterozygous variants (0 skipped due to missing genotypes)
[W::hts_idx_load3] The index file is older than the data file: HCC1395_tumor.recal.bam.bai
Number of supplementary alignments: 0
Number of non-singleton groups: 11286
Skipped 0 groups
Found 46339 reads covering 197 variants
Kept 8797 reads that cover at least two variants each
Selected 472 most phase-informative reads covering 90 variants
Best-case phasing would result in 33 non-singleton phased blocks (0 singletons). 
Phasing 1 sample by solving the MEC problem ...
Largest block contains 7 variants (7.8% of accessible variants) between position 10462806 and 10462873
WARNING: Ignoring existing phasing information found in input VCF (PS tag exists).

# Resource usage
Maximum memory usage: 0.158 GB
Time spent reading BAM/CRAM:                   22.3 s
Time spent parsing VCF:                         0.0 s
Time spent selecting reads:                     0.5 s
Time spent phasing:                             0.3 s
Time spent writing VCF:                         0.0 s
Time spent finding components:                  0.0 s
Time spent on rest:                             0.1 s
Total elapsed time:                            23.2 s