coyote3

DNA Workflow

This chapter documents the full DNA analyst workflow, including what happens after each user action.

Related diagrams:

Entry point

What loads when the page opens

When you open a DNA sample, Coyote3:

  1. Loads sample, assay config, and schema.
  2. Resolves assay group and subpanel.
  3. Merges sample filters with assay defaults.
  4. Builds effective gene set from ASP (Assay Specific Panel) genes + selected ISGL (In Silico Gene List) + ad-hoc genes.
  5. Builds SNV query and loads variants.
  6. Adds blacklist flags and global annotation/tier data.
  7. Loads other enabled sections from assay config:
    • CNV
    • TRANSLOCATION
    • BIOMARKER
    • FUSION (if configured)

DNA list page sections

Typical sections on list_variants_vep.html:

Filters and sample settings behavior

On the DNA list page:

Important behavior:

Variant-level actions

Open variant detail:

Available actions on variant detail:

Bulk actions

Route:

Bulk actions can apply/remove:

CNV actions

CNV detail route:

Common CNV actions:

Translocation actions

Translocation detail route:

Common translocation actions:

Auto-tier behavior while reviewing

When variants are shown, Coyote3 checks annotation history and chooses latest matching classification.

Matching priority:

  1. HGVSp
  2. HGVSc
  3. genomic identity (CHR:POS:REF/ALT)

Scoping:

If no direct scoped class is found, additional classification lookup may provide assay-scoped fallback.

Report preview and save

Preview:

Save:

Both use the same payload builder, so preview and saved report content are aligned.

Save path also persists:

Practical productive workflow

  1. Start from /samples/live.
  2. Open sample and confirm assay/subpanel context.
  3. Validate effective genes before deep review.
  4. Tier only after reviewing existing global annotations and assay/subpanel fit.
  5. Add concise interpretation comments.
  6. Preview report and verify sections.
  7. Save report and verify sample appears in done/reported list.