def test_load_tcga_paad():
    maf_filename = 'data/PAAD.maf'
    hla_filename = 'data/PAAD.hla'
    alleles = read_hla_file(hla_filename)
    transcripts_df, vcf_df, variant_report = load_file(maf_filename)
    assert len(vcf_df) > 0
    assert len(transcripts_df) > 0
Exemple #2
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def test_load_tcga_paad():
    maf_filename = 'data/PAAD.maf'
    hla_filename = 'data/PAAD.hla'
    alleles = read_hla_file(hla_filename)
    transcripts_df, vcf_df, variant_report = load_file(maf_filename)
    assert len(vcf_df) > 0
    assert len(transcripts_df) > 0
Exemple #3
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def test_read_hla():
    # contains two C identical C alleles
    hla_filename = 'data/SKCM.hla'
    alleles = read_hla_file(hla_filename)
    print alleles
    assert alleles == [
        'HLA-A*01:01', 'HLA-A*03:01', 'HLA-B*08:01', 'HLA-B*07:02',
        'HLA-C*07:02', 'HLA-C*07:02'
    ]
def test_read_hla():
    # contains two C identical C alleles
    hla_filename = 'data/SKCM.hla'
    alleles = read_hla_file(hla_filename)
    print alleles
    assert alleles == [
        'HLA-A*01:01',
        'HLA-A*03:01',
        'HLA-B*08:01',
        'HLA-B*07:02',
        'HLA-C*07:02',
	'HLA-C*07:02'
   ]