hseeker 0.1.0

HSeeker — H-DNA / Triplex Mirror Repeat Detector — fast C core with Python API

HSeeker

HSeeker is a fast, cross-platform Python package for detecting H-DNA (intramolecular triplex DNA) and mirror repeat structures in genomic sequences. It ships a compiled C extension (_hdna) as its computational core and exposes both a clean Python API and a drop-in CLI replacement for the original findHDNA binary.

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Table of Contents

1. Biological Background
2. Algorithm Overview
3. Installation
4. Quick Start
5. Python API
6. Command-Line Interface
7. Output Format
8. Parameter Reference
9. Understanding the Results
10. Performance Notes
11. Development & Testing
12. Benchmarks
13. Citation
14. License

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1. Biological Background

H-DNA (also called intramolecular triplex DNA) forms when a single DNA strand folds back onto the Watson–Crick duplex and inserts into the major groove via Hoogsteen or reverse-Hoogsteen hydrogen bonds. The result is a three-stranded helical segment joined by a short single-stranded hinge loop.

  5'─────[left arm]─────[spacer]─────[right arm]─────3'
                    ╲       (hinge)      ╱
                     ╲__triplex core___╱

Structural requirements

Requirement	Rationale
Mirror repeat geometry	Both arms must be approximate reverse complements of each other (reading the sequence in the same 5′→3′ direction, the two halves mirror each other).
Compositional asymmetry (purity)	Stable H-DNA requires a dominantly purine (GA-rich) or dominantly pyrimidine (CT-rich) arm to enable Hoogsteen pairing.
Short spacer / hinge	Loops >10 bp introduce thermodynamic strain that precludes stable folding. Typical genomic H-DNA has spacers of 0–7 bp.
Arm length ≥ 6 bp	Shorter tracts lack the binding energy for stable triplex formation.

Biological significance

H-DNA is found throughout eukaryotic and prokaryotic genomes and has been associated with:

• Transcription regulation — GA-rich mirror repeats in promoters modulate RNA Pol II stalling.
• Genomic instability — H-DNA structures are linked to DNA breakage and large-scale rearrangements.
• Epigenetic features — Triplex-forming regions are enriched at nucleosome-depleted regulatory elements.
• Human disease — Polypurine tracts implicated in cancer, neurodegenerative diseases, and trinucleotide expansion disorders.

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2. Algorithm Overview

HSeeker implements a center-outward biologically informed heuristic that supports imperfect mirrors and compositional tolerance, enabling detection of biologically realistic H-DNA candidates.

How it works

1. Candidate generation — For every position ctr (potential center of the hinge) and every spacer length sp from 0 to maxspacer:
   • A left pointer starts at ctr and moves left (toward 5′).
   • A right pointer starts at ctr + sp + 1 and moves right (toward 3′).
2. Outward extension — At each step k, the base pair (dna[left], dna[right]) is compared:
   • If equal: mirror match.
   • If different: mismatch counter is incremented.
   • Arm composition (fraction GA or CT) is tracked continuously.
3. Threshold evaluation — After every base pair beyond minrep, the algorithm evaluates:

$$\text{mirror identity} = 1 - \frac{\text{mismatches}}{k}$$

$$\text{purity} = \max!\left(\frac{\text{GA count}}{k},\ \frac{\text{CT count}}{k}\right)$$

If both $\text{mirror identity} \geq 1 - \texttt{mismatch}$ and $\text{purity} \geq \texttt{purity}$, the current arm length is recorded as a valid candidate.

4. Longest-arm retention — For each (ctr, sp) pair, only the longest valid arm is kept. This ensures no redundant shorter arms at the same position.
5. Overlap removal — After scanning the full sequence, overlapping hits are resolved by keeping the longest arm first; ties are broken by shorter spacer.

is_perfect classification

A hit is classified as is_perfect = True only when:

• The arm is 100% pure (either all GA or all CT), and
• The mirror identity is 100% (zero mismatches).

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3. Installation

From PyPI (recommended)

pip install hseeker

Binary wheels are provided for CPython 3.9–3.13 on Linux (x86_64, aarch64), macOS (x86_64, arm64, universal2), and Windows (AMD64). No compiler is needed.

From source

git clone https://github.com/Georgakopoulos-Soares-lab/HDNAhunter.git
cd HDNAhunter
pip install .

A C compiler (GCC, Clang, or MSVC) is required when building from source. The C extension compiles automatically during pip install.

Development install

pip install -e ".[dev]"

This installs pytest, build, twine, and cibuildwheel in addition to the package itself.

Dependencies

Package	Version	Purpose
Python	≥ 3.9	Core runtime
pandas	≥ 1.5	DataFrame output helper

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4. Quick Start

In Python

import hseeker

# Scan a raw sequence string
hits = hseeker.scan_sequence(
    "GGGAAAGGGTTTTCCCAAACCC",
    minrep=10,
    maxspacer=10,
    purity=0.90,
    mismatch=0.10,
)
for h in hits:
    print(h["start"], h["end"], h["arm_length"], h["is_perfect"], h["total_score"])

# Scan an entire FASTA file (all hits collected into a list)
hits = hseeker.scan_fasta("genome.fa", minrep=10, purity=0.90)

# Memory-efficient streaming alternative — yields one hit at a time
for hit in hseeker.scan_fasta_iter("genome.fa", minrep=10, purity=0.90):
    print(hit["seq_id"], hit["start"], hit["end"])

# Multi-core parallel scan — all chromosomes scanned concurrently
hits = hseeker.scan_fasta_parallel("genome.fa", minrep=10, purity=0.90)
hits = hseeker.scan_fasta_parallel("genome.fa", minrep=10, workers=4)

From the command line

# Minimal — scan test.fa and write test_HDNA.tsv
hseeker -seq test.fa -out test

# Strict mode — exact mirror, 100 % pure
hseeker -seq genome.fa -out strict -purity 1.0 -mismatch 0.0

# Relaxed mode — allow up to 10 % mismatch, 90 % purity
hseeker -seq genome.fa -out relaxed -purity 0.90 -mismatch 0.10

# Verbose output, longer arms only
hseeker -seq genome.fa -out long -minrep 10 -maxrep 1000 -v

---

5. Python API

hseeker.scan_sequence

hseeker.scan_sequence(
    seq: str,
    *,
    minrep: int = 10,
    maxrep: int = 1000,
    maxspacer: int = 10,
    purity: float = 0.90,
    mismatch: float = 0.10,
    remove_overlaps: bool = True,
    seq_offset: int = 1,
    score: bool = True,
) -> list[dict]

Scan a single DNA string for H-DNA mirror repeat motifs. The C core runs with the Python GIL released, so other threads remain unblocked during the scan.

Parameters — see Parameter Reference.

Returns a list of hit dictionaries. Each dictionary contains all fields described in Output Format.

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hseeker.scan_fasta

hseeker.scan_fasta(
    path: str | Path,
    *,
    minrep: int = 10,
    maxrep: int = 1000,
    maxspacer: int = 10,
    purity: float = 0.90,
    mismatch: float = 0.10,
    remove_overlaps: bool = True,
    score: bool = True,
) -> list[dict]

Scan every record in a FASTA file. Adds a seq_id key to each hit dict. Genomic offsets are parsed automatically from UCSC/Ensembl-style headers (>seqid:start-end); other headers default to offset 1.

---

hseeker.scan_fasta_iter

hseeker.scan_fasta_iter(
    path: str | Path,
    *,
    minrep: int = 10,
    maxrep: int = 1000,
    maxspacer: int = 10,
    purity: float = 0.90,
    mismatch: float = 0.10,
    remove_overlaps: bool = True,
    score: bool = True,
) -> Generator[dict, None, None]

Streaming alternative to scan_fasta. Yields one hit dict at a time, keeping only a single record's worth of hits in memory at any moment. Use this for large FASTA files (e.g. whole-genome scans) where accumulating all hits at once would exhaust RAM. scan_fasta is implemented as list(scan_fasta_iter(...)) and is provided for backward compatibility.

---

hseeker.scan_fasta_parallel

hseeker.scan_fasta_parallel(
    path: str | Path,
    *,
    minrep: int = 10,
    maxrep: int = 1000,
    maxspacer: int = 10,
    purity: float = 0.90,
    mismatch: float = 0.10,
    remove_overlaps: bool = True,
    workers: int | None = None,
    chunk_size: int = 1_000_000,
    score: bool = True,
) -> list[dict]

Scans all FASTA records in parallel using a thread pool. Because the C scan releases the GIL, threads achieve true CPU parallelism on the heavy computation.

Records longer than chunk_size are split into overlapping chunks and scanned in parallel. With the default chunk_size=1_000_000, even single-chromosome genomes like E. coli (4.6 Mb) are split into multiple chunks for thread-level parallelism. On a 5-core machine this achieves ~4.6× speedup over the sequential scan on a single-chromosome genome.

workers defaults to os.cpu_count(). Pass an explicit integer to cap thread count (e.g. workers=4). Results are returned in the same record order as the input FASTA file.

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6. Command-Line Interface

hseeker -seq <FASTA> -out <PREFIX> [options]

or equivalently:

python -m hseeker -seq <FASTA> -out <PREFIX> [options]

Positional / required arguments

Argument	Description
-seq FASTA	Path to the input FASTA file. May contain one or multiple records. Both single-line and wrapped FASTA are supported.
-out PREFIX	Output file prefix. The tool writes <PREFIX>_HDNA.tsv.

All optional arguments

Argument	Type	Default	Description
-minrep INT	int	10	Minimum arm length in base pairs. Arms shorter than this are not reported, even if they satisfy all other criteria. Increasing this value reduces noise and focuses on structurally stable, longer H-DNA elements (recommended ≥ 10 for whole-genome scans).
-maxrep INT	int	1000	Maximum arm length cap. The algorithm stops extending an arm beyond this length. Set higher for repetitive regions; setting it very high increases runtime without improving sensitivity for typical H-DNA.
-maxspacer INT	int	10	Maximum spacer / hinge loop length in base pairs. The spacer is the single-stranded loop between the two mirror arms. H-DNA with spacers > 10 bp is thermodynamically unfavourable in vivo; the default of 10 captures biologically realistic hinge loops. Setting this to 0 requires the two arms to be immediately adjacent.
-purity FLOAT	float	0.90	Minimum compositional purity of each arm (0.0–1.0). The arm must be ≥ purity fraction GA (purine) or ≥ purity fraction CT (pyrimidine). Set to 1.0 to require a perfectly pure homopurine/homopyrimidine arm. Lower values (e.g. 0.80) increase sensitivity at the cost of more false positives.
-mismatch FLOAT	float	0.10	Maximum mirror mismatch fraction (0.0–1.0). Fraction of base positions in the arm where dna[left] ≠ dna[right] (i.e. the mirror is broken). 0.0 requires a perfect mirror; 0.10 allows 1 mismatch per 10 bp. This parameter is independent of purity — both must be satisfied simultaneously.
-skipoverlap	flag	(off)	Skip overlap removal. By default, overlapping hits are collapsed to the longest arm (ties broken by shortest spacer). Pass this flag to disable overlap removal and receive every raw hit at every (center, spacer) combination that passes the thresholds. Useful for statistical analyses or when you want to inspect the full hit landscape.
-score	flag	(on)	Apply thermodynamic stability scoring. Enables stacking and pairing score computation for each hit. Pass -no-score to disable and keep only the core detection columns.
-workers INT	int	(all cores)	Parallel worker threads. The CLI uses scan_fasta_parallel internally and defaults to all available CPU cores. Set this to a lower value to cap CPU usage, or to 1 to run single-threaded.
-v	flag	(off)	Verbose mode. Prints progress information to stderr. Useful for monitoring large jobs.

CLI examples

# 1. Basic scan
hseeker -seq genome.fa -out results

# 2. Strict mode — exact mirror, 100 % pure
hseeker -seq genome.fa -out strict -purity 1.0 -mismatch 0.0

# 3. Whole-genome scan with minimum arm length 10 for high confidence
hseeker -seq hg38.fa -out hg38_hdna -minrep 10 -purity 0.85 -v

# 4. Exploratory scan — very permissive, keep all raw hits
hseeker -seq region.fa -out explore -purity 0.80 -mismatch 0.20 \
            -minrep 8 -maxspacer 10 -skipoverlap

# 5. Long perfect H-DNA only
hseeker -seq genome.fa -out perfect -purity 1.0 -mismatch 0.0 \
            -minrep 12 -maxspacer 3

# 6. Verbose output to monitor progress on a large genome
hseeker -seq hg38.fa -out hg38 -minrep 8 -v 2>progress.log

# 7. Use 8 worker threads instead of all cores
hseeker -seq hg38.fa -out hg38 -workers 8

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7. Output Format

The CLI writes a tab-separated file (<prefix>_HDNA.tsv). scan_fasta() returns the same data as a list of dictionaries. Column descriptions:

Column	Type	Description
seq_id	str	FASTA record identifier
source	str	Always findHDNA (for GFF3 / database compatibility)
start	int	1-based, inclusive genomic start of the left arm
end	int	1-based, inclusive genomic end of the right arm
arm_length	int	Length of each arm in bp (both arms are always equal length)
spacer_length	int	Length of the hinge loop between the two arms in bp
total_length	int	arm_length × 2 + spacer_length — full motif span
ga_pct	float	Percentage of G+A (purine) bases in the right arm (0–100)
ct_pct	float	Percentage of C+T (pyrimidine) bases in the right arm (0–100)
mirror_identity	float	Fraction of mirror positions that match × 100 (0–100)
is_perfect	bool	True if arm is 100 % pure and mirror identity is 100 %
left_arm	str	Sequence of the left arm (5′→3′)
spacer	str	Sequence of the hinge loop
right_arm	str	Sequence of the right arm (5′→3′)
full_sequence	str	Complete motif sequence: left_arm + spacer + right_arm
stacking_score	float	Stacking energy score from the triplex stability model (None if scoring was disabled)
pairing_score	float	Pairing energy score from the triplex stability model (None if scoring was disabled)
total_score	float	Combined stacking + pairing score (None if scoring was disabled)
putative_triplex	str	Adjusted triplex sequence in left_arm[spacer]right_arm notation after score-based boundary optimisation

Example output

seq_id  source    start  end  arm_length  spacer_length  total_length  ga_pct   ct_pct   mirror_identity  is_perfect  left_arm  spacer  right_arm  full_sequence  stacking_score  pairing_score  total_score  putative_triplex
chr1    findHDNA  1001   1020  7           6              20            85.71    14.29    100.0            False       gggaaat   tttttt  taaaggg    gggaaattttttttaaaggg  35.0            42.3           77.3          gggaaat[tttttt]taaaggg

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8. Parameter Reference

Parameter	API name	CLI flag	Type	Default	Valid range	Notes
Minimum arm length	minrep	-minrep	int	10	≥ 1	Arms shorter than this are discarded entirely
Maximum arm length	maxrep	-maxrep	int	1000	≥ minrep	Hard cap on extension; rarely needs changing
Maximum spacer	maxspacer	-maxspacer	int	10	≥ 0	Set to 0 for zero-loop (adjacent arms) only
Purity threshold	purity	-purity	float	0.90	0.0–1.0	Fraction GA or CT required in arm
Mismatch tolerance	mismatch	-mismatch	float	0.10	0.0–1.0	Fraction of arm positions allowed to mismatch the mirror
Overlap removal	remove_overlaps	-skipoverlap (inverts)	bool	True	—	When True, keeps only the longest non-overlapping hit
Sequence offset	seq_offset	(automatic in CLI)	int	1	≥ 1	1-based start coordinate of seq[0]; used for correct genomic coordinates
Worker threads	(CLI only)	-workers	int	all cores	≥ 1	Number of parallel threads used by the CLI (via scan_fasta_parallel)
Stability scoring	score	-score / -no-score	bool	True	—	When True, computes stacking and pairing scores and an optimised triplex sequence for each hit. Scoring adds stacking_score, pairing_score, total_score, and putative_triplex columns to the output.

Choosing parameters for your use case

Genome-wide survey (high confidence)

minrep=10, maxrep=1000, maxspacer=10, purity=0.90, mismatch=0.10

Exploratory / maximum sensitivity

minrep=8, maxrep=1000, maxspacer=10, purity=0.80, mismatch=0.20

Downstream ML or statistical analysis (all raw candidates)

remove_overlaps=False, skipoverlap (CLI)

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9. Understanding the Results

Interpreting ga_pct and ct_pct

These two values always sum to ≤ 100 %. The difference is due to ambiguous or masked bases:

• GA-rich arm (ga_pct ≈ 80–100): purine-rich tract → H-r triplex (Pu·Pu·Py)
• CT-rich arm (ct_pct ≈ 80–100): pyrimidine-rich tract → H-y triplex (Py·Pu·Py)
• Mixed (neither > purity): filtered out unless purity is set very low

mirror_identity vs purity

mirror_identity measures how closely the two arms are mirror images of each other. A value of 100 means every base on the left arm is identical to its mirror partner on the right arm. A value of 80 means 80 % of positions match (1 mismatch per 5 bp in a 6-mer arm). This is independent of purity: a CT-rich arm with one GA interruption could still have 100 % mirror identity.

is_perfect flag

is_perfect = True is a stringent classification reserved for hits that are both:

1. 100 % pure — every base in the arm is GA, or every base is CT.
2. 100 % mirror-symmetric — no mismatches between the two arms.

These are the most likely candidates for stable H-DNA structures.

Scoring results (stacking_score, pairing_score, total_score)

When scoring is enabled (default), each hit is passed through a thermodynamic stability model that evaluates the energetic favourability of triplex formation. The model assigns a pairing score based on Hoogsteen base-pair complementarity (G–G and A–A matches contribute positively; mismatches incur a penalty) and a stacking score that rewards consecutive GA–GA dinucleotide stacks. The two components are summed to produce a total score; higher values indicate more stable candidate triplexes. A total score ≥ 60 is the recommended threshold for filtering to high-confidence, thermodynamically stable H-DNA candidates.

The scoring pass also produces a putative_triplex field — the motif sequence in left_arm[spacer]right_arm notation — whose arm/spacer boundaries may differ from the original detection because the scorer re-optimises the boundary to maximise the combined stacking and pairing signal.

Scoring can be disabled at the API level (score=False) or via the CLI flag -no-score, which removes the four scoring columns from the TSV output.

Overlap removal behaviour

When remove_overlaps=True (default), two hits overlap if their genomic ranges on the DNA share at least one base. Among all overlapping hits, the one with the longest arm is retained. Ties are broken by choosing the shorter spacer.

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10. Performance Notes

• The C extension releases the Python GIL during scanning, enabling multi-threaded use.
• scan_fasta_parallel(path, workers=N) with default chunk_size=1_000_000 achieves ~N× speedup on N-core machines even for single-chromosome genomes like E. coli (4.6 Mb), which are automatically split into overlapping chunks.
• The CLI uses scan_fasta_parallel by default, automatically parallelising across all available CPU cores. A single human chromosome (≈ 250 Mb, chr1) processes in ~78 seconds on 16 cores. Use -workers N to limit parallelism.
• The internal hit buffer is capped at 1,000,000 hits per scan_sequence call. For whole-genome scans, use scan_fasta_parallel (which splits each contig into overlapping chunks) rather than concatenating chromosomes into a single string.
• Memory usage is approximately O(n_hits × 200 bytes) plus the sequence string itself.
• N bases in the sequence (N, n) break arm extension, as per the original algorithm.

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11. Development & Testing

Running the test suite

# Install dev dependencies first
pip install -e ".[dev]"

# Run all 134 tests
pytest -v tests/

The test suite (tests/test_hdna.py) covers:

• Empty / trivial inputs
• Known GA and CT mirror motifs with exact expected values
• Strict mode (purity=1.0, mismatch=0.0) and relaxed mode
• Coordinate offset propagation (seq_offset)
• Multi-record FASTA parsing, scan_fasta_iter streaming generator, and scan_fasta_parallel
• Parallel chunking edge cases: boundary hits, tiny chunks, N-bases near boundaries, determinism
• Overlap removal correctness
• Parameter validation (out-of-range inputs)
• Exact field values for reference sequences
• Purity and maxspacer boundary conditions
• Case insensitivity (mixed-case input)
• Output field self-consistency (start + total_length - 1 == end)
• Flanking N base handling
• is_perfect flag logic
• Mirror identity with known mismatch counts
• Determinism (identical calls produce identical results)
• CLI end-to-end integration

Project structure

hseeker/
├── src/
│   └── hseeker/
│       ├── _hdna.c          # C extension — core algorithm
│       ├── __init__.py      # Python API (scan_sequence, scan_fasta, scan_fasta_iter, scan_fasta_parallel)
│       └── __main__.py      # CLI entry point (hseeker / python -m hseeker)
├── tests/
│   └── test_hdna.py         # 134 comprehensive tests (pytest)
├── .github/
│   └── workflows/
│       └── build_wheels.yml # CI: build binary wheels + sdist, publish to PyPI
├── pyproject.toml           # Build config (setuptools, cibuildwheel, pytest)
├── setup.py                 # C extension definition
├── MANIFEST.in              # sdist file inclusion rules
└── README.md

Building wheels locally

# Build the current platform wheel
pip install build
python -m build --wheel

# Build all platform wheels (requires Docker on Linux/Windows)
pip install cibuildwheel
cibuildwheel --platform linux

Adding a new test

Tests live in tests/test_hdna.py. Each section focuses on one concern. Add new sequences as module-level constants and group related assertions under a descriptively named function. Run pytest -v tests/test_hdna.py -k <your_test_name> to run just your new test.

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13. Benchmarks

benchmarks/benchmark.py is a CLI-only end-to-end benchmark that downloads real hg38/GRCh38 chromosomes from NCBI and measures wall time, peak RSS, and TSV throughput for the full hseeker pipeline (FASTA read → scan → overlap removal → scoring → TSV write).

Setup

pip install -e ".[dev]"

Running

# All 24 chromosomes (~3 GB download on first run)
python benchmarks/benchmark.py

# Single chromosome quick test
python benchmarks/benchmark.py --chromosomes chr1

# Save machine-readable results to JSON
python benchmarks/benchmark.py --chromosomes chr1 --json results.json

# Write a Markdown report
python benchmarks/benchmark.py --chromosomes chr1 --report report.md

# Force re-download
python benchmarks/benchmark.py --no-cache

Chromosome FASTA files are cached in benchmarks/data/ (gitignored). When chr1, chr2, and chr3 are all present, the benchmark automatically builds a concatenated chr1_2_3.fa for multi-record throughput testing.

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13. Citation

If you use HSeeker in published research, please cite:

Georgakopoulos-Soares Lab, UT Austin.
HSeeker: fast, cross-platform detection of H-DNA and mirror repeat structures in genomic sequences.
https://github.com/Georgakopoulos-Soares-lab/HDNAhunter

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14. License

MIT License — see LICENSE for full text.

Copyright © 2024 Georgakopoulos-Soares Lab, UT Austin.