Import Features from a GTF, GFF3, or BED File
How do I import features into a SnapGene file from a GTF, GFF3, or BED file?
GTF, GFF3, and BED are standard files formats for storing feature information in plain text.
GFF stands for Generic Feature Format. A GFF3 file describes features with coordinates corresponding to a specific reference sequence. See this link for more information.
GTF is similar to GFF3 and is sometimes referred to as GFF2.5. See this link for more information.
BED stands for Browser Extensible Data. This format was developed for the human genome project. See this link for more information.
A GTF, GFF3, or BED file can describe features for multiple reference sequences. Note that SnapGene cannot currently import multi-sequence GTF, GFF3, or BED files.
A GTF or GFF3 file may include one or more reference sequences as embedded FASTA data. Note that SnapGene cannot use a FASTA sequence embedded in GTF or GFF3 files as a reference.
In most cases a GFF3 file is accompanied by a separate reference file in FASTA format.
Import or Open a Reference Sequence
Import or open a reference sequence. For example, drag a reference sequence file onto the SnapGene launch window, or click File → Open to locate and import the reference sequence file.
You may need to specify whether the sequence should be linear or circular.
Import the GFF3, GTF, or BED File
Ensure that the reference sequence is the front SnapGene window, then click Features → Import Features → Import Features from a [BED, GFF3, or GTF] File... .
Use the Browse button to locate and load the feature file. Click OK to import the feature information into the reference sequence file.
The features described in the GTF, GFF3, or BED file will be displayed on the reference sequence in Map and Sequence views, and will be listed in Features view. Click File → Save to save the annotated sequence as a SnapGene file.