Ultima Genomics

{{ report_title }}

Tumor-Informed Minimal Residual Disease Detection · Whole Genome Sequencing

Sample {{ basename }}
Report Date {{ report_date }}
Detection Result
{% if detection.detected is true %}
{{ detection.call }}
{% elif detection.detected is false %}
{{ detection.call }}
{% else %}
{{ detection.call }}
{% endif %}
ctDNA VAF {{ vaf_str }}
p-value (Binomial) {{ binom_p_str }} Binom(N={{ detection.n_effective }}, p_err={{ noise_rate_str }})
Supporting Reads {{ detection.matched_supporting_reads }}
{% if detection.jeffreys_prior_applied %}
ℹ No background reads observed in synthetic controls — noise rate estimated via Jeffreys prior (p_err = {{ noise_rate_str }}).
{% endif %} {% if detection.n_synthetic_controls < 20 %}
⚠ Only {{ detection.n_synthetic_controls }} synthetic controls — p-value reliability is reduced.
{% endif %}
{% if detection.qc_checks %}
QC Checks
{% for check in detection.qc_checks %}
{% if check.passed %}✅{% else %}⚠️{% endif %} {{ check.label }} {{ check.value_str }} threshold: {{ check.threshold_str }}
{% endfor %}
{% endif %}
Assay Metrics
Signature Size
{{ "{:,}".format(detection.signature_size) }}
filtered loci
Mean Coverage
{{ "%.1f"|format(detection.mean_coverage) }}×
at signature loci
Corrected Coverage
{{ "{:,.0f}".format(detection.corrected_coverage) }}
effective depth × loci
Coverage Correction Ratio
{{ "%.2f"|format(denom_ratio) }}
corrected / original coverage
Patient vs. Controls
Patient vs. Controls
Patient: matched patient signature.
Synthetic control signatures: Signatures drawn from db_control.
Blue violin: Fitted Binomial, according to synthetic control error-rates: Binom(N={{ detection.n_effective }}, p_err={{ noise_rate_str }}).
⎯⎯ Detection threshold (min VAF for Binomial p < {{ "%.0f"|format(detection.alpha * 100) }}%).
·–· Sample-specific LOD = {{ lod_str }} — minimum VAF detectable at {{ "%.0f"|format(detection.lod_recall * 100) }}% recall / {{ "%.0f"|format(detection.lod_fpr * 100) }}% FPR for this patient’s signature size and coverage.
Cohort control signatures.
{% if sbs6_vaf_plots or sbs96_plots %}
Signature Profile & VAF
{% for img in sbs6_vaf_plots %}
SBS profile and VAF distribution
{% endfor %} {% if sbs96_plots %} {% for img in sbs96_plots %}
SBS96 mutational profile
COSMIC-format SBS96 profile from all filtered signature variants. 96 trinucleotide channels grouped by substitution type, normalised to pyrimidine strand.
{% endfor %} {% endif %}
{% endif %} {% if intersection_af_img %}
cfDNA Intersection Allele Fraction
cfDNA Intersection AF
Allele-fraction distribution at signature loci with ≥1 supporting cfDNA read. Red: patient signature loci (signal). Blue: control signature loci (noise).
{% endif %} {% if read_length_img %}
Read Length Distribution
Read length distribution
Read length distribution of cfDNA reads at signature loci (after read filter). Red: patient signature loci. Blue: control signature loci. Shorter fragment lengths are enriched in ctDNA due to nucleosomal positioning.
{% endif %} {% if intersection_snvq_img %}
cfDNA Intersection SNVQ Distribution
cfDNA Intersection SNVQ
SNVQ score distribution of cfDNA reads at signature loci (after read filter). Red: patient signature loci. Blue: control signature loci. Higher SNVQ indicates higher confidence in the SNV call.
{% endif %} {% if lq_fraction_hist_img %}
LQ-Reads Fraction per Locus
LQ-reads fraction histogram
Per-locus fraction of reads failing the read filter (LQ reads) for matched signature loci. Blue: loci kept (LQ fraction ≤ threshold). Red: loci excluded by the noisy-loci filter. Dashed line: threshold{% if thresh_noise_lq_reads is not none %} ({{ thresh_noise_lq_reads }}){% endif %}.
{% endif %} {% if supporting_reads_hist_img %}
Alt-Supporting Reads per Variant Locus
Alt-supporting reads histogram
Distribution of alt-supporting cfDNA read counts per signature locus (after read filter). Red: patient loci — signal. Blue: control loci — noise baseline. Loci with zero supporting reads are not shown; their count is annotated in the plot.
{% endif %} {% if filter_funnel %}
Signature Filter Funnel
{% for row in filter_funnel %} {% endfor %}
StepCount% Funnel% Pass
{{ row.step }} {% if row.desc %}
{{ row.desc }}
{% endif %}
{{ "{:,}".format(row.count) }} {{ "%.1f%%"|format(row.pct_funnel) if row.pct_funnel is not none else "" }} {{ "%.1f%%"|format(row.pct_pass) if row.pct_pass is not none else "" }}
{% endif %} {% if read_funnel %}
Read Filter Funnel
{% for row in read_funnel %} {% endfor %}
StepCOUNT (READS)%FUNNEL (READS)%PASS (READS)COUNT (LOCI)%FUNNEL (LOCI)%PASS (LOCI)
{{ row.step }} {% if row.desc %}
{{ row.desc }}
{% endif %}
{{ "{:,}".format(row.count) }} {{ "%.1f%%"|format(row.pct_funnel) if row.pct_funnel is not none else "" }} {{ "%.1f%%"|format(row.pct_pass) if row.pct_pass is not none else "" }} {{ "{:,}".format(row.loci_count) if row.loci_count is not none else "" }} {{ "%.1f%%"|format(row.pct_funnel_loci) if row.pct_funnel_loci is not none else "" }} {{ "%.1f%%"|format(row.pct_pass_loci) if row.pct_pass_loci is not none else "" }}
{% endif %}
For Research Use Only. This report is intended solely for research purposes and has not been validated for clinical diagnostic use. It does not constitute a clinically validated test and should not be used to guide clinical decisions without independent clinical validation. Results may not be accurate for all sample types or conditions.