Record
File Format Converter
Read a file in one format and write it in another without a round trip through a server. Join and complement locations, qualifiers and multi-segment features survive the conversion, because the parsers were ported and tested against real files rather than written to a summary of the spec.
Nine real annotation files: GFF3 · GTF · BED · EMBL across three divisions and three molecule types, the 5′-UTR introns most parsers have never met, and the JBEI registry’s own XML
What it does
- 01Read GenBank, FASTA, FASTQ, EMBL, GFF3, GTF, BED, SnapGene .dna and JSON
- 02Write GenBank, FASTA, EMBL, GFF3, GTF, BED, JSON, and the two binary formats the tools that own them will not export to each other: SnapGene .dna and Serial Cloner .xdna
- 03Join and complement locations preserved, including multi-segment CDS features
- 04Feature-only files (GFF3, GTF, BED) opened on an unknown-base sequence spanning their features
- 05BED12 block columns expanded into multi-segment locations
- 06Qualifiers preserved on round trip
- 07What each target would drop stated before you download it, and a target the record cannot produce disabled with the reason
- 08Converted in the browser tab, with no upload and no project to create first
What it runs on
The parsers are ports of CGParse and the Teselagen bio-parsers, tested against the upstream corpora. The panel runs on @ports/protein.
Everything runs client-side. Files are parsed in the browser and projects are saved on this machine, so an unpublished sequence is never uploaded.
Questions
- Does converting lose my features?
- No. Features, their locations including join and complement, and their qualifiers are carried through, and multi-segment CDS features stay multi-segment.
- Can I open a GFF3 with no sequence in it?
- Yes. A feature-only file opens on an unknown-base sequence spanning its features, so the annotations can be inspected and re-exported.
Also searched as
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