GFF3 Merge Tool
A focused tool for researchers and bioinformaticians to merge GFF3 files quickly, ensuring consistent feature coordinates and attributes across datasets.
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About This Tool
Core concept and workflow: the engine parses each feature, groups by key fields, and merges entries according to a defined policy. When features share an ID and type but differ in attributes, non-conflicting attributes are merged; conflicting values can be logged and optionally resolved by user-defined rules. The merged output is sorted by seqid, start, and end, with header lines preserved.
Who benefits and differentiators: scientists performing cross-dataset integration, annotation curation teams, and bioinformatics engineers building reproducible pipelines gain a reliable, auditable merge process. Unique value includes strict GFF3 validation, transparent merge logs, support for filtering (by sequence, type, or source), and an explicit report of changes to aid provenance and audits.
Use cases include integrating annotations from multiple assemblies, consolidating feature catalogs for a genome project, and preparing data for comparative genomics studies. The tool emphasizes data integrity, deterministic results, and compliance with GFF3 standards to reduce post-processing errors.
How to Use
- Provide inputs by uploading GFF3 files or pasting their content.
- Configure merge options: select filtering by seqid or type and attribute merging strategy.
- Run merge to produce a single consolidated GFF3 file.
- Review the summary of merged features and any conflicts detected.
- Download or save the merged GFF3 file and optional statistics.
- Validate the output against the GFF3 specification to confirm compliance.
Frequently Asked Questions
Find Quick Answers
What formats are supported?
How are attribute conflicts handled?
Is the output a valid GFF3 file?
Can filters be applied during merge?
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