Gene sharing: Unrelated samples

Description   Prerequisites   Dialog   Practical tips   Algorithm

Description

Identification of genes where all the affected have variants compatible with the disease model. Unafected samples are used as an additional filter.

Prerequisites

The analysis can be applied to any variant files loadable in Filtus, as long as the genotype format is correctly given in the input settings. In particular, samples from different variant files can be analyzed together, even if the files have different formats.

For Recessive analysis, all involved samples must have a well defined gene column (specified in the input settings).

Dialog

Gene sharing dialog
Model
The genetic disease model, either Dominant, Recessive (which includes both compound heterozygous and homozygous models) and Recessive homoz (homozygous only).

Affected
Indicate the affected samples, separated by comma. Samples can be specified in various ways:

Healthy
Indicate the unaffected/control samples. Syntactic choices are as for the Affected field.

Practical tips

Tip 1: The identified genes are displayed in the main window, sorted on the p-value. You can sort on any column by right clicking on the column header.

Tip 2: Right click on a gene to view the relevant variants in that gene. You can also view the variants in all identified genes simultaneously, or in the genes on top of the list.

The algorithm

todo