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A standalone and free application to explore genetics variations from VCF file

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Probably related to #101. By reading the documentation of SnpEff & SnpSift: https://pcingola.github.io/SnpEff/examples/ By the way, **I strongly recommend writing such a tutorial before any new implementation of anything; it...

enhancement
help wanted
question
low-priority

All history is display in Edit Only concerned history must be displayed

Because creating source from samples is mostly used to select all variants for these samples, but without any other filters. To create a source from samples with existing filters, it's...

enhancement
medium priority

Add a plugin to show history, by modified table

enhancement
core

Add an "Open Config" item in Cutevariant menu "File" to open another config file. The idea is to switch between configuration, and especially presets, to create a exploration/validation context

enhancement
core

Create history table to track changes in validation fields

core
high-priority

In order to homogenize validation fields in tables - table "samples" ``` valid INTEGER DEFAULT 0, tags TEXT DEFAULT '', comment TEXT DEFAULT '', ``` - table "sample_has_variant" ``` {...

core
high-priority

A plugin to check miss-validated variants: - "Variants already validated in some samples but not all of them" ``` SELECT distinct(variant_id) FROM sample_has_variant WHERE sample_has_variant.classification IN (2) AND sample_has_variant.gt >=1...

enhancement
medium priority

When a VCF is imported and contains a sample that already exists in the project, classification of the sample is set to default value (0, unlock)

When importing a VCF which include an existing variant and sample association, fields count_var, count_het... are recalculated by incrementing number, which is not correct. Test by creating a db with...