GFFx is a high-performance, Rust-based toolkit for extracting and querying annotations from GFF3 files. It supports fast indexing and feature retrieval with several subcommands. It can be used both as a command-line tool and as a Rust library.

Benchmarking runtime and memory usage of ID-based feature extraction
Added two useful functionalities: coverage for calculating breadth of coverage and depth for calculating depth of coverage from BAM/SAM/CRAM or BED files on a GFF file.
Added a sample functionality for random downsampling of feature groups from each chromosome at equal ratios.
Updated module organization and source code directory layout to conform to the Rust 2024 edition guidelines for module visibility (pub) and path imports.
GFFx version 0.4.0
sample - Randomly downsample feature groups
cargo install gffx # install to default location (~/.cargo/bin)
cargo install gffx --root /your/path # optional: install to custom location
git clone https://github.com/Baohua-Chen/GFFx.git
cd GFFx
cargo build --release
# Optionally copy the binary
cp target/release/gffx /your/path
gffx <SUBCOMMAND> [OPTIONS]
Available subcommands:
indexBuilds index files from a GFF file to accelerate downstream operations.
gffx index [OPTIONS] --input <INPUT>
Options:
| Option | Description |
|---|---|
-i, --input |
Input GFF file |
-a, --attribute |
Attribute key to extract (default: gene_name) |
-v, --verbose |
Enable verbose output |
-h, --help |
Print help |
intersectExtracts models intersecting with regions from a GFF file, either from a single region or a BED file.
gffx intersect [OPTIONS] --input <INPUT> <--region <REGION>|--bed <BED>>
Options:
Required
| Option | Description |
| --------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| -r, --region <REGION> | Single region in chr:start-end format |
| -b, --bed <BED> | BED file containing multiple regions |
Note: Exactly one of
--regionor--bedmust be specified.
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| -e, --entire-group | Enable the "entire-group" mode. Return entire gene models or feature groups |
| | for all matched features, instead of only the directly matched features. |
| -v, --invert | Invert selection (exclude matched features) |
| -T, --types <TYPES> | Filter output to include only features of specified types (e.g., gene,exon) |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
| (one of) | |
| -c, --contained | Only keep features fully contained within the region |
| -C, --contains-region | Only keep features that fully contain the region |
| -O, --overlap | Keep features that partially or fully overlap (default mode) |
extractExtracts annotation models by feature ID(s), including their parent models.
gffx extract [OPTIONS] --input <INPUT> <--feature-file <FEATURE_FILE>|--feature-id <FEATURE_ID>>
Options:
Required
| Option | Description |
| ---------------------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| (one of) | |
| -f, --feature-id <FEATURE_ID> | Extrach by a single feature id |
| -e, --feature-file <FEATURE_FILE> | Extrach by a BED file containing multiple regions |
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| -e, --entire-group | Enable the "entire-group" mode. Return entire gene models or feature groups |
| | for all matched features, instead of only the directly matched features. |
| -T, --types <TYPES> | Filter output to include only features of specified types (e.g., gene,exon) |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
searchSearches for features using a specified attribute value and retrieves the full annotation models.
gffx search -a geneX -i input.gff
Options:
Required
| Option | Description |
| ---------------------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| (one of) | |
| -a, --attr <ATTRIBUTE_VALUE> | Search a single attribute value/pattern |
| -A, --attr-list <ATTRIBUTE_LIST> | Search attribute values/patterns defined in a text file |
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| -e, --entire-group | Enable the "entire-group" mode. Return entire gene models or feature groups |
| | for all matched features, instead of only the directly matched features. |
| -r, --regex <REGEX> | Enable regex matching for attribute values |
| -T, --types <TYPES> | Filter output to include only features of specified types (e.g., gene,exon) |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
coverageCompute coverage breadth across genomic feature.
gffx coverage -i input.gff -s source.bam
Options:
Required
| Option | Description |
| ---------------------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| -s, --source `
` | Source file in BAM/SAM/CRAM or BED format |
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| -e, --entire-group | Enable the "entire-group" mode. Return entire gene models or feature groups |
| | for all matched features, instead of only the directly matched features. |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
depthCompute coverage depth across genomic feature.
gffx depth -i input.gff -s source.bam
Options:
Required
| Option | Description |
| ---------------------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| -s, --source `
` | Source file in BAM/SAM/CRAM or BED format |
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| --bin-shift <BIN_SHIFT> | Bin width parameter (2^k bp) for spatial bucketing of features and queries. |
| | Choose k so that a typical read and feature span ~1–2 bins [default: 12] |
| -e, --entire-group | Enable the "entire-group" mode. Return entire gene models or feature groups |
| | for all matched features, instead of only the directly matched features. |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
sampleRamdomly downsample feature groups.
gffx sample -i input.gff -r 0.33
Options:
Required
| Option | Description |
| ---------------------------------------- | ------------------------------------------------------------ |
| -i, --input <INPUT> | Input GFF file path |
| -r, --ratio <RATIO> | Ratio of downsampling, should be between 0 and 1 |
Optional
| Option | Description |
| ------------------------- | ------------------------------------------------------------------------------ |
| -o, --output <OUT> | Output file path (default: stdout) |
| -t, --threads <NUM> | Number of threads [default: 12] |
| -V, --verbose | Enable verbose output |
| -h, --help | Show help message |
```bash
gffx index -i genes.gff -a gene_name
gffx intersect --region chr1:10000-20000 -i genes.gff -o out.gff -F