Filters

Use the Filters tab in the Filters/Presets panel to narrow numerous variants down to those most relevant to your case.

Filter categories

Filter group
Purpose

Narrow variants by sequencing quality metrics such as depth, mapping quality, and confidence grade

Filter by allele frequency and genotype counts from public databases (e.g., gnomAD, ExAC) or your lab’s internal controls

Focus on specific variant categories (SNVs, indels, CNVs, SVs, STRs, mtDNA)

Select by predicted consequences on genes or proteins, ACMG classes, or database classifications

Apply computational prediction scores for pathogenicity, conservation, splicing, or missense effects

Restrict results to genes of interest, such as disease–associated, candidate, ACMG actionable, or cancer–related genes

Highlight variants in genes with known disease associations matching the proband’s phenotypes

Filter variants according to inheritance patterns consistent with family genotypes and phenotypes

Select by genotype status (Het, Hom, Hemi) in specific samples

Show variants tagged by users, AI shortlist, or flagged at the organization level

Filtering modes

Quality, Polymorphism, Variant effect, In silico prediction, and Evidence & Tags filters can operate in either a simple or advanced mode.

Use simple mode for quick, high-level filtering. For more detailed filtering with expanded options, choose advanced mode to gain deeper control over filter parameters.

Filters actions menu

When the Filters tab of the Filters/Presets panel is selected, click the vertical ellipsis (⋮) in the top-left corner to access the following actions:

  • Clear: Clears all filters and displays all variants in the case

  • Reset to default: Clears all filters and applies the default settings:

    • Quality: Moderate/High

    • Variant Severity: Low/Moderate/High

    • Proband Zygosity: Het/Hom

  • Save as preset: Saves the current filter configuration as a new preset

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