nonhuman-screen 0.1.0

Classify sequencing reads by non-human taxonomic content (kraken2), including the allele-based non-human fraction of reads supporting a variant.

nonhuman-screen

Classify sequencing reads by non-human taxonomic content using kraken2, and reduce the per-read verdicts to a non-human fraction (NHF) plus per-domain breakdowns (bacterial / archaeal / fungal / protist / viral / UniVec-Core).

The headline capability is the allele-based NHF: given a BAM/CRAM and a variant, compute the non-human fraction of the reads that support that variant's ALT allele — in one call, no boilerplate:

from nonhuman_screen import classify_variant_alt_reads

v = classify_variant_alt_reads(
    "sample.bam", "kraken2_db", "chr1", 12345, "A", "T", ref_fasta="ref.fa",
)
v.nonhuman_fraction   # 0.0–1.0 over ALT-supporting reads
v.fractions.bacterial # per-domain breakdown
v.supporting_reads    # denominator

nonhuman-screen is sample-agnostic: it classifies whatever reads you hand it and never asks whose they are. The same call works on a proband, a parent, a tumour, or a plain FASTQ — so it can back higher-level analyses (e.g. flagging inherited variant calls that are actually parental contamination) without knowing anything about pedigrees.

Extracted from kmer-denovo-filter, where this methodology was originally developed, so it can be reused independently.

How it works (in one paragraph)

Reads are written to a temporary FASTQ and classified by kraken2's LCA algorithm. Each read's assigned taxid is mapped to a domain using the database's nodes.dmp taxonomy. A read counts as non-human only if it is classified and lies outside the human lineage, outside the human clade, and outside UniVec-Core. Two conservative guards reduce false positives: a human-homology guard (any k-mer voting for human, taxid 9606, drops the read from every non-human numerator — important for integrating viruses such as HBV/HPV/ERVs) and UniVec-Core exclusion (synthetic vector/adapter sequences, taxid 81077, are tracked separately and never counted as contamination). See docs/methodology.md.

Install

pip install nonhuman-screen           # core engine (standard library only)
pip install 'nonhuman-screen[bam]'    # + BAM/CRAM & allele-based NHF (pysam)

The bam extra is required for the BAM/allele helpers and for the nonhuman-screen CLI (both classify modes import pysam). The core install covers only Kraken2Runner.classify_sequences on in-memory reads.

You also need the kraken2 binary on PATH and a kraken2 database — see docs/database.md.

Usage

Allele-based NHF for many variants (batched — one kraken2 call)

from nonhuman_screen import classify_variants_alt_reads

variants = [("chr1", 12345, "A", "T"), ("chr2", 999, "G", "GAC")]  # pos 0-based
for v in classify_variants_alt_reads("sample.bam", "kraken2_db", variants,
                                      ref_fasta="ref.fa"):
    print(v.variant_key, v.nonhuman_fraction, v.supporting_reads)

The reads supporting all variants' ALT alleles are gathered and classified in a single kraken2 invocation (its database load dominates runtime), then split back per variant. You never re-implement fetch/allele-filter/classify yourself.

Classify an arbitrary set of reads

from nonhuman_screen import Kraken2Runner

result = Kraken2Runner("kraken2_db").classify_sequences(
    {"read1": "ACGT...", "read2": "TTGCA..."}
)
result.nonhuman_fraction        # 0.0–1.0
result.fractions()              # TaxonomicFractions(nonhuman=…, bacterial=…, …)
result.taxonomy_available       # False if nodes.dmp was missing (fractions unreliable)
result.nonhuman_read_names      # set of read names

Command line

# Per-variant allele NHF table (headline)
nonhuman-screen classify \
    --bam sample.bam --kraken2-db kraken2_db --ref-fasta ref.fa \
    --variants candidates.vcf.gz --out-prefix sample_contam
# -> sample_contam.variant_nhf.tsv, sample_contam.summary.json

# Whole-BAM summary
nonhuman-screen classify --bam sample.bam --kraken2-db kraken2_db

See docs/cli.md.

Coordinate convention

All pos arguments in the Python API are 0-based (pysam reference coordinates); variant keys are "{chrom}:{pos}:{ref}:{alt}". The CLI reads a VCF and handles the conversion for you.

API summary

Symbol	Needs [bam]	Purpose
Kraken2Runner.classify_sequences(seqs)	no	Classify {name: seq} → ClassificationResult
ClassificationResult	no	Per-domain read-name sets, counts, fractions(), nonhuman_fraction, taxonomy_available
TaxonomicFractions	no	Per-domain fractions; from_result / over_reads
read_supports_alt(read, variant_pos, ref, alt)	no	Does an aligned read carry the ALT allele?
parse_kmer_votes(kmer_string)	no	Parse kraken2 per-read k-mer detail into taxid votes
VariantNHF	no	Result of the allele-based helpers: variant_key, nonhuman_fraction, supporting_reads, fractions, to_dict() (pos 0-based)
classify_variant_alt_reads(...)	yes	Allele-based NHF for one variant → VariantNHF
classify_variants_alt_reads(...)	yes	Batched allele-based NHF for many variants
classify_reads_from_bam(...)	yes	Classify reads by name and/or locus
reads_supporting_alt(...)	yes	Read names supporting an ALT allele

Docker

The included Dockerfile installs the pinned kraken2 (v2.17.1) and the package with the [bam] extra:

docker build -t nonhuman-screen .

docker run --rm -v "$PWD:/data" nonhuman-screen \
    classify --bam /data/sample.bam --kraken2-db /data/kraken2_db \
             --variants /data/calls.vcf.gz --out-prefix /data/contam

The image entrypoint is nonhuman-screen; mount your BAM and kraken2 database in. You still supply the kraken2 database yourself (see docs/database.md).

License

MIT — see LICENSE.