{{ sample.display_name }} |
{{ sample.genotype_call }} |
{% if sample.allele_depths %}
{% for number in sample.allele_depths %}
{% if number == -1 %}
N/A
{% else %}
{{ number }}
{% endif %}
|
{% endfor %}
{% else %}
N/A |
N/A |
{% endif %}
{% if variant.category == "snv" and variant.chromosome in ["MT","M"] %}
{% if sample.alt_frequency and sample.alt_frequency != -1 %}
{{ (100*sample.alt_frequency)|round(2) }}%
{% else %}
N/A
{% endif %}
|
{% endif %}
{% if variant.category == "cancer" %}
{% set cancer_var = namespace() %}
{% if sample.sample_id == variant.tumor.ind_id %}
{% set cancer_var.vaf = variant.tumor.alt_freq|round(4) %}
{% elif sample.sample_id == variant.normal.ind_id %}
{% set cancer_var.vaf = variant.normal.alt_freq|round(4) %}
{% else %}
{% set cancer_var.vaf = "N/A" %}
{% endif %}
{{ cancer_var.vaf }} |
{% else %}
{% if variant.category == "sv" %}
{% if sample.genotype_quality not in ["None", None, "-1", -1] %}
{{ sample.genotype_quality }}
{% else %}
N/A
{% endif %} (VQ
{% if variant.quality not in ["None", None, "-1", -1] %}
{{variant.quality}}
{% else %}
N/A
{% endif%})
{% elif variant.category == "str" %}
{{ sample.so }}
{% else %}
{{ sample.genotype_quality }}
{% endif %}
|
{% endif %}
{% endfor %}