FAIR-bioHeaders Tools
Convert and validate FAIR-bioHeaders Reference genome (FHR) metadata in JSON,
YAML, JSON-LD, FASTA, GFA, and HTML microdata. See
FHR-Specification for the
schema and metadata design. This is the fair-bioheaders package, version
0.5.0, formerly the FHR File Converter (fhr); see
Renamed from fhr.
Install
For a published release:
python -m pip install fair-bioheaders
For this checkout and its development checks (Python 3.9 or later):
python -m pip install poetry
poetry install
poetry run pytest
poetry run ruff check .
poetry run isort . --check-only
poetry run black . --check
Commands
bioheaders convert examples/example.fhr.yaml /tmp/example.fhr.json
bioheaders validate /tmp/example.fhr.json
bioheaders combine examples/example.fhr.yaml genome.fasta -o genome.fhr.fasta
bioheaders verify genome.fhr.fasta
bioheaders strip genome.fhr.fasta genome.stripped.fasta
bioheaders combine examples/example.fhr.yaml assembly.gfa -o assembly.fhr.gfa
bioheaders verify assembly.fhr.gfa
bioheaders strip assembly.fhr.gfa assembly.stripped.gfa
combine, strip, and verify (also called checksum) take the FASTA or GFA
type from the sequence file's extension, ignoring .gz or .bgz; give
--type fasta or --type gfa for stdin or other extensions. bioheaders --version prints the version and bioheaders COMMAND --help describes each
command. The original commands remain available with the same options and output:
bioheaders command |
Original command |
|---|---|
convert INPUT OUTPUT |
fhr-convert |
validate INPUT |
fhr-validate |
combine METADATA SEQUENCE |
fhr-fasta-combine, fhr-gfa-combine |
strip INPUT [OUTPUT] |
fhr-fasta-strip, fhr-gfa-strip |
verify INPUT |
fhr-fasta-validate, fhr-gfa-validate |
convert INPUT OUTPUT detects .json, .yaml/.yml, .jsonld, .fasta/.fa/.fna,
.gfa, and .html from extensions. It validates metadata before writing output;
FASTA/GFA output contains a metadata header only. To include sequence data, use
combine METADATA SEQUENCE [-o OUTPUT], whose default output is SEQUENCE.fhr.fasta
or SEQUENCE.fhr.gfa with the last extension replaced. Existing FHR header lines
are replaced. Inputs are not overwritten by sequence helpers.
strip INPUT [OUTPUT] writes to stdout if OUTPUT is omitted. Only FHR-prefixed
lines are removed; other bytes, including ordinary comments and CRLF endings,
are preserved. validate checks metadata, while verify (fhr-fasta-validate,
fhr-gfa-validate) also verifies the exact-byte file checksum. Failures exit
with status 1.
FASTA/GFA commands stream their input in 1 MiB chunks, so memory use does not grow with file size (about 35 MB peak for a 1 GB FASTA). Validate reads the file once; combine reads it twice. FHR header lines are limited to 16 MiB in total. Outputs are written to a temporary file in the destination directory and then renamed, so a failed command leaves no partial output.
Compressed files and pipes
bioheaders combine examples/example.fhr.yaml genome.fa.gz # writes genome.fhr.fasta.gz
bioheaders verify genome.fhr.fasta.gz
bioheaders strip genome.fhr.fasta.gz genome.stripped.fa.gz
zcat genome.fa.gz | bioheaders combine --type fasta examples/example.fhr.yaml - > genome.fhr.fasta
curl -sL https://example.org/genome.fhr.fasta.gz | bioheaders verify --type fasta -
bioheaders convert genome.fhr.fasta.gz - --to json
bioheaders convert - metadata.yaml --from json < metadata.json
Gzip input, including multi-member gzip and BGZF, is recognized by its magic
bytes rather than its extension and decompressed as it streams. The checksum
covers the decompressed FASTA/GFA bytes, so genome.fa and any gzip or BGZF
compression of it have the same checksum. A corrupt or truncated gzip file is an
error. Formats are taken from the extension before .gz or .bgz.
Outputs whose path ends in .gz or .bgz are written as BGZF, which gzip,
zcat, bgzip, and htslib read. A combine without -o keeps the input's
compression extension. Other outputs, and stdout, are never compressed. Note that
samtools faidx (and tools built on htslib, such as bcftools and pysam's
FastaFile) rejects FASTA files containing ; lines, compressed or not. Keep
the FHR file as the record of provenance and index a stripped copy:
bioheaders strip genome.fhr.fa.gz genome.fa.gz # writes BGZF
samtools faidx genome.fa.gz # .fai and .gzi
The stripped file has the same sequence bytes; bioheaders verify on the FHR
file still checks the original. Which other tools accept FHR files is surveyed in
TOOL_COMPATIBILITY.md;
support for leading ; lines in htslib is proposed in
samtools/htslib#2103.
- reads stdin or writes stdout: the input of verify, strip, combine (the
sequence), convert, and validate, and the output of strip, convert, and
combine -o. Combine of stdin writes stdout by default. Convert and validate
need --from FORMAT for stdin and convert needs --to FORMAT for stdout
(json, yaml, jsonld, fasta, gfa, or html); the bioheaders sequence commands
need --type for stdin. Stdin is read
once: combine spools the stripped sequence to a temporary file in TMPDIR (as
large as the sequence) while hashing it. Strip from stdin to stdout writes as it
reads, so an error late in the input can follow partial output; check the exit
status. Strip of a file to stdout still checks the whole file before writing.
JSON-LD
bioheaders convert examples/example.fhr.json example.fhr.jsonld
bioheaders convert example.fhr.jsonld back.json
bioheaders convert --export-context export.yaml examples/example.fhr.json page.jsonld
A .jsonld file is the FHR record with its own keys, an embedded JSON-LD context and
@type on the record (Dataset) and its nested nodes, so the same document is FHR
metadata and schema.org linked data. The format is defined in FHR-Specification
docs/JSONLD.md,
and examples/example.fhr.jsonld is byte-identical to the specification's example. The
context is bundled (bioheaders/fhr.context.jsonld, a copy of the specification's
jsonld/fhr.context.jsonld) and never fetched; writing and reading the canonical form need no
extra package, and everything works offline.
- Authors are typed
Personwith an ORCID iD,Organizationwith a ROR ID, and otherwiseAgent(not classified). Adocumentationvalue that is an absolute URL is written assubjectOf, text asdocumentation(schema:description). - Nested keys that the context does not define, such as
taxon.checksum, are kept and reported:FHR: JSON-LD: taxon.checksum has no JSON-LD term; linked-data consumers will ignore it. --export-context FILE(JSON-LD output only, provisional) reads a YAML or JSON mapping with the dataset'sid, landing-pageurlandkeywords, which are not FHR fields. The output then claims Bioschemas Dataset 1.0-RELEASE conformance (conformsTo) only when every minimum property is present, and otherwise names the missing ones.- Reading accepts the canonical form (rule J1): the bundled context, embedded or by its
raw-main URL, and no JSON-LD keyword except
@type(and a root@id).@contextand@typeare set aside,subjectOfbecomesdocumentation, and the export terms are set aside with a warning; the rest is validated like JSON. - Other JSON-LD forms (expanded, compacted with another context such as a schema.org
@vocab, or one record in@graph) are read by JSON-LD expansion (rules J3 to J5). This needs thejsonldextra, PyLD, on Python 3.10 or later:pip install "fair-bioheaders[jsonld]". Contexts are served only from the bundled copy, so a remote context such ashttps://schema.org/is refused (FHR: JSON-LD context is not available offline: https://schema.org/). A term that maps to no FHR field fails the read (FHR: JSON-LD term not in the FHR mapping: http://schema.org/keywords (at the record));convertandvalidatetake--ignore-unknown-termsto report such terms as warnings instead. The document must describe exactly one record.
FAIR header assessment
bioheaders assess GCF_000002985.6_WBcel235_genomic.gff.gz # terminal report
bioheaders assess --format json annotations.gff3.gz > report.json # machine-readable
bioheaders assess --related genomic.fa.gz annotations.gff3.gz # check the recorded genome link
bioheaders assess --recursive --pairs pairs.tsv --output reports/9.1.0 release-9.1.0/
assess reads the header of a FASTA, GFF3, GAF, VCF, GFA or other text file (gzip and BGZF
too) and reports, for each of the 41 RDA FAIR Data Maturity Model indicators, a status
(evidenced, partially evidenced, not evidenced, not applicable or not assessed) with
the header lines it rests on and, for each gap, a line to add in the file's own convention. It
is a checklist, not a score: nothing adds the statuses up. The guideline behind it is
FHR-Specification
docs/FAIR_HEADER_GUIDELINE.md,
and the specification's assessment/ fixtures pin the expected results
(feature 010).
- A FAIR-bioHeaders header gets a separate conformance result against the bundled schema; the schema URL in the header is never fetched.
--related FILEverifies the links the header records (FHR checksum, SeqCol digest, VCF##contigMD5s, assembly accessions) against a related file, usually the genome, and reports name and length agreement separately as circumstantial evidence.- Batch mode (several files, or a directory with
--recursive) needs--output DIR. It writes one JSON and one Markdown report per file, mirroring the input tree, andsummary.json,summary.mdandsummary.tsvwith per-indicator counts.--pairsmaps derived files to related files (derived<TAB>related, relative to the directory);--include/--excludeselect files and--jobssets the number of processes. Re-running on unchanged files gives byte-identical output, sodiffshows what changed between releases. - Offline by default. No network access is made unless
--onlineis given. Then only the identifiers and URLs found in the header are resolved (DOIs through doi.org, CURIEs through identifiers.org, http(s) URLs as given), never file contents; private and loopback addresses are refused, and the report marks the results as time-dependent. - Exit codes: 0 assessed (whatever the statuses), 1 an input could not be read, 2 usage error,
3 with
--fail-on-mismatchwhen a recorded link does not match the related file.
scripts/bench_assess.py (checkout only) times batch mode on a synthetic 200-file release.
Indicator identifiers and titles from: FAIR Data Maturity Model Working Group (2020). FAIR Data Maturity Model. Specification and Guidelines. Research Data Alliance. doi:10.15497/rda00050. Licensed CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). File-header interpretations are adaptations by FAIR-bioHeaders and are not endorsed by the RDA.
Python
from bioheaders import fhr
metadata = fhr()
with open("examples/example.fhr.yaml", encoding="utf-8") as stream:
metadata.input_yaml(stream)
metadata.fhr_validate()
print(metadata.output_json())
Input methods accept text, UTF-8 bytes, or readable streams. Optional fields stay
absent until supplied. The mapping is preserved across supported format round
trips; HTML values are escaped and explicitly typed. Keywords can initialize an
instance (fhr(genome="example")), and fields remain accessible as attributes.
The installed schema is loaded from package resources rather than the working
directory, so commands work outside the checkout. No schema is downloaded at runtime.
bioheaders.cli holds the command implementations and the byte-level helpers
(checksum, combine, strip_header, open_input, write_to, and others).
JSON-LD uses output_jsonld(export=None) and
input_jsonld(stream, ignore_unknown_terms=False, warn=None). The
bioheaders.jsonld module is a provisional API: CONTEXT (the bundled context),
KNOWN_CONTEXT_URLS, to_jsonld(data, export=None),
from_jsonld(document, *, ignore_unknown_terms=False, warn=None),
is_canonical(document), unmapped_keys(data) and bioschemas_missing(document).
bioheaders.assess is a provisional API: assess_file(path, related=None, online=False, record_limit=1000) returns one report and assess_release(paths, output_dir, pairs=None, jobs=None, online=False) writes a release's reports and returns its summary, as plain dicts
that follow the JSON Schemas in bioheaders/assess/data/.
Renamed from fhr
In 0.4.0 the PyPI package fhr was renamed fair-bioheaders, the Python package
fhr was renamed bioheaders, and the repository moved from FHR-File-Converter
to FAIR-bioHeaders-Tools
(old links redirect). The new names leave room for other FAIR-bioHeaders header
types. Nothing that worked with 0.3 stops working:
- The eight
fhr-*commands are unchanged and print no deprecation notices, so scripts and pipelines that read their output or stderr keep working. They are not deprecated, but new scripts can usebioheaders. import fhr,from fhr import fhr, andfrom fhr.cli import ...still work:fhrandfhr.cliare the same module objects asbioheadersandbioheaders.cli. Importingfhremits oneDeprecationWarning; replacefhrwithbioheadersin imports. Thefhrmetadata class keeps its name.pip install fhrinstallsfhr, a compatibility package without code that requires the same version offair-bioheaders, so existing requirements andpip install -U fhrkeep working. Preferfair-bioheadersin new requirements. The compatibility package also installs thefhr-*commands, so if you uninstallfhr0.4 later, restore them withpython -m pip install --force-reinstall --no-deps fair-bioheaders.- In an environment that still has
fhr0.3, runpython -m pip uninstall fhrbeforepython -m pip install fair-bioheaders(or upgrade withpython -m pip install -U fhr); otherwise the oldfhrpackage files shadow the new compatibility module. - Citations and Zenodo DOIs are unchanged.
Checksum helpers require SHA-512/256 support in the Python build. Some Apple system Python builds omit it; use an OpenSSL-enabled Python distribution. Metadata conversion and validation do not require that hash implementation.
v0.3 compatibility and identity
- Required fields and
schemaVersion: 1remain unchanged since v0.3.0. assemblySoftwareaccepts a legacy string or optional structured software objects with name, URI, version, and command options.assemblyProtocolis a URI.vitalStats.N90is base pairs;vitalStats.gcContentis 0–100 percent.- Optional
seqcol_idstores a supplied 32-character base64url top-level refget digest. The converter preserves it; it does not compute or verify SeqCol identity. - Checksums use base64 SHA-512/256 of all original file bytes except the one scalar checksum header line, including its newline. Metadata is covered. MD5 hex and payload-only checksums from old examples are not valid v0.3 checksums; recombine metadata with the original sequence file to calculate the new value.
- The checksum value must be a single-line scalar on the checksum line. Header lines must be UTF-8 and must not contain U+0085, U+2028, or U+2029. FASTA/GFA files must not begin with a UTF-8 byte order mark. Other sequence bytes may use any encoding.
- Metadata must be JSON-compatible: duplicate keys, YAML anchors, aliases, and merge keys are rejected.
;~/#~lines must form the leading header block, before the first FASTA>line or the first GFA record line; ordinary comments and blank lines may be mixed in. A;~/#~line after sequence data, including a concatenated second file, is an error.- HTML exports use FHR item scopes and
data-fhr-typeannotations for lossless arrays, numbers, objects, and strings. External microdata must represent nested items properly; incomplete legacy markup may need regeneration. - Incomplete constructors now emit missing fields rather than empty defaults. Validate after loading to obtain actionable schema errors. Obsolete positional constructor arguments should be converted to keywords.
See the format reference and release notes. JSON/YAML/HTML example identifiers are synthetic. The FASTA/GFA fixtures contain verified FHR checksums; their SeqCol IDs are placeholders.
Docker
docker build -t fair-bioheaders-tools .
docker run --rm fair-bioheaders-tools --help
The image runs fhr-convert; use --entrypoint bioheaders for the other
commands. Mount inputs/outputs into the container for conversion. See
CONTRIBUTING, CODE_OF_CONDUCT,
SECURITY, and AGENTS for project guidance.
Citing FHR
Chicago bibliography entries are used below. Cite the published paper for a general description of FHR; cite the specification or converter when using that resource directly. The software and specification links are concept DOIs; for a specific release, use the corresponding version DOI from Zenodo. Authors and years follow the records resolved by the concept DOIs at the v0.3 documentation update, and can change as later records are published.
Published paper
Wright, Adam, Mark D. Wilkinson, Christopher Mungall, Scott Cain, Stephen Richards, Paul Sternberg, Ellen Provin, Jonathan L. Jacobs, Scott Geib, Daniela Raciti, Karen Yook, Lincoln Stein, and David C. Molik. “FAIR Header Reference Genome: A TRUSTworthy Standard.” Briefings in Bioinformatics 25, no. 3 (2024): bbae122. https://doi.org/10.1093/bib/bbae122.
Specification
Molik, David. FHR Specification. Data set. 2022. https://doi.org/10.5281/zenodo.6762549.
Converter
Molik, David, and Adam Wright. FHR File Converter. Computer software. 2024. https://doi.org/10.5281/zenodo.6762547.
Machine-readable entries are maintained in FHR-Citation.
Licensing
New project contributions from March 2025 onward use MPL-2.0. David Molik left USDA in February 2025. Historical USDA public-domain material remains public domain within the United States; its original notice is preserved in LICENSE. Previously granted permissions and third-party terms remain intact. The project includes both historical material and subsequent MPL-2.0 contributions; file notices and history identify provenance.
Metadata
Release files for fair-bioheaders 0.5.0
For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.
Source distribution (sdist)
| File | Size | Uploaded | |
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| fair_bioheaders-0.5.0.tar.gz | 109.4 kB | Details |
Built distribution (wheel)
| File | Interpreter | ABI | Platform | Reset |
|---|---|---|---|---|
| fair_bioheaders-0.5.0-py3-none-any.whl | Python 3 | none | any | Details |
Total release size: 226.8 kB
Release files / fair_bioheaders-0.5.0.tar.gz
| Download URL | fair_bioheaders-0.5.0.tar.gz |
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