Project Scope
What this project aims to be
This project aims to be a practical desktop tool for inspecting, editing, aligning, classifying, visualizing, and exporting sequence data.
The primary target is Sanger and FASTA-based workflows, especially where users need to quickly review sequence differences, inspect mutation sites, compare regions, and prepare tables or figures.
In scope
- Sanger sequence review
- FASTA import and export
- editable DNA/RNA/protein sequence viewing
- aligned sequence inspection
- site-based mutation inspection
- region-based variability visualization
- label and typing rule-based classification
- similarity-based grouping
- simple tree-assisted grouping
- grouped sequence export
- table and figure export
Not the primary scope
The project is not intended to replace full NGS pipelines or large-scale genome analysis platforms.
The following areas are not primary targets:
- raw NGS read processing
- FASTQ quality control
- read mapping
- variant calling from mapped reads
- de novo assembly
- professional phylogenetic inference pipelines
- full plasmid cloning simulation
- primer design automation
Some related features may be added later as helper functions, but the main focus remains practical sequence inspection and visualization.