deacon

Crates.iodeacon
lib.rsdeacon
version0.10.0
created_at2025-03-14 13:41:09.482083+00
updated_at2025-09-01 15:20:25.698513+00
descriptionFast DNA sequence filtering with minimizers
homepagehttps://github.com/bede/deacon
repositoryhttps://github.com/bede/deacon
max_upload_size
id1592222
size3,168,782
Bede Constantinides (bede)

documentation

README

CI status Crates.io version Conda version Crates.io downloads Conda downloads biorXiv preprint

Deacon

Logo

Search and depletion of FASTA/FASTQ files and streams using accelerated minimizer matching. Default parameters balance sensitivity and specificity for the application of microbial metagenomic host depletion, for which a validated prebuilt index is available. Classification sensitivity, specificity and memory requirements may be tuned by varying k-mer length (-k), window size (-w), and the two match thresholds (-a and -r). Minimizer k and w are chosen at index time, while the match thresholds can be chosen at filter time. To be considered a match, sequences must meet both an absolute threshold (-a, default 2 minimizer hits) and a relative threshold (-r, default 0.01 or 1% of minimizers). Paired sequences are also supported: a match in either mate causes both mates in the pair to be retained or discarded; deacon filter retains only matches by default (search mode) and discards matches in --deplete mode. Deacon reports filtering performance during execution and optionally writes a JSON --summary upon completion. Sequences can optionally be renamed using --rename for privacy and smaller file sizes. Gzip, zst and xz compression formats are natively supported and detected by file extension.

Deacon is capable of filtering compressed long reads at >500Mbp/s and indexing a human genome in <30s (Apple M1). Filtering at >2Gbp/s is possible with uncompressed input. Peak memory usage during filtering is 5GB for the default panhuman index. Use Zstandard (zst) compression and/or pipe output to an external compressor such as pigz for best performance.

Benchmarks for panhuman host depletion of complex microbial metagenomes are described in a preprint. Among tested approaches, Deacon with the panhuman-1 (k=31, w=15) index exhibited the highest balanced accuracy for both long and short simulated reads. Deacon was however less specific than Hostile for short reads.

[!IMPORTANT] Deacon is actively developed and unstable. Take note of software and index version(s) used in order to guarantee reproducibility of your results. Carefully review the CHANGELOG when updating. Version 0.7.0 introduced a new index container format that is incompatible with prior versions. Please report any problems you encounter by creating an issue or using the email address in my profile.

Install

cargo Crates.io version

cargo install deacon

conda/mamba/pixi Conda version

conda install -c bioconda deacon

Usage

Indexing

Use deacon index build to quickly build custom indexes. For human host depletion, the prebuilt validated panhuman index is recommended, available for download below from Zenodo or faster object storage. Object storage is provided by the ModMedMicro research unit at the University of Oxford.

deacon index build chm13v2.fa > human.k31w15.idx

# Discard very low complexity minimizers
deacon index build -e 0.5 chm13v2.fa > human.k31w15e5.idx

Prebuilt indexes

Name/URL Composition Minimizers Subtracted minimizers Size Date
panhuman-1 (k=31, w=15) Cloud, Zenodo HPRC Year 1CHM13v2.0GRCh38.p14 - bacteria (FDA-ARGOS) - viruses (RefSeq) 409,913,780 20,781 (0.0051%) 3.7GB 2025-07
panmouse-1a (k=31, w=15, e=0.5) Cloud GRCm39PRJEB47108 - bacteria (FDA-ARGOS) - viruses (RefSeq) 548,331,948 8,246 (0.0015%) 4.6GB 2025-08

Filtering

The main command deacon filter accepts an index path followed by up to two query FASTA/FASTQ file paths, depending on whether query sequences originate from stdin, a single file, or paired input files. Paired queries are supported as either separate files or interleaved stdin, and written interleaved to either stdout or file, or else to separate paired output files. For paired reads, distinct minimizer hits originating from either mate are counted. By default, query sequences must meet both an absolute threshold of 2 minimizer hits (-a 2) and a relative threshold of 1% of minimizers (-r 0.01) to pass the filter. Filtering can be inverted for e.g. host depletion using the --deplete (-d) flag. Gzip, Zstandard, and xz compression formats are detected automatically by file extension. Use Zstandard compression rather than Gzip where possible for best performance.

Examples

# Keep only human sequences
deacon filter panhuman-1.k31w15.idx reads.fq.gz > filt.fq

# Host depletion using the panhuman-1 index and default thresholds
deacon filter -d panhuman-1.k31w15.idx reads.fq.gz -o filt.fq.gz

# Max sensitivity with absolute threshold of 1 and no relative threshold
deacon filter -d -a 1 -r 0 panhuman-1.k31w15.idx reads.fq.gz -o filt.fq.gz

# More specific 10% relative match threshold
deacon filter -d -r 0.1 panhuman-1.k31w15.idx reads.fq.gz > filt.fq.gz

# Stdin and stdout
zcat reads.fq.gz | deacon filter -d panhuman-1.k31w15.idx > filt.fq

# Faster Zstandard compression
deacon filter -d panhuman-1.k31w15.idx reads.fq.zst -o filt.fq.zst

# Fast gzip with pigz
deacon filter -d panhuman-1.k31w15.idx reads.fq.gz | pigz > filt.fq.gz

# Paired reads
deacon filter -d panhuman-1.k31w15.idx r1.fq.gz r2.fq.gz > filt12.fq
deacon filter -d panhuman-1.k31w15.idx r1.fq.gz r2.fq.gz -o filt.r1.fq.gz -O filt.r2.fq.gz
zcat r12.fq.gz | deacon filter -d panhuman-1.k31w15.idx - - > filt12.fq

# Save summary JSON
deacon filter -d panhuman-1.k31w15.idx reads.fq.gz -o filt.fq.gz -s summary.json

# Replace read headers with incrementing integers
deacon filter -d -R panhuman-1.k31w15.idx reads.fq.gz > filt.fq

# Only look for minimizer hits inside the first 1000bp per record
deacon filter -d -p 1000 panhuman-1.k31w15.idx reads.fq.gz > filt.fq

# Debug mode: see sequences with minimizer hits in stderr
deacon filter -d --debug panhuman-1.k31w15.idx reads.fq.gz > filt.fq

Command line reference

Filtering

$ deacon filter -h
Keep or discard DNA fastx records with sufficient minimizer hits to the index

Usage: deacon filter [OPTIONS] <INDEX> [INPUT] [INPUT2]

Arguments:
  <INDEX>   Path to minimizer index file
  [INPUT]   Optional path to fastx file (or - for stdin) [default: -]
  [INPUT2]  Optional path to second paired fastx file (or - for interleaved stdin)

Options:
  -o, --output <OUTPUT>
          Path to output fastx file (or - for stdout; detects .gz and .zst) [default: -]
  -O, --output2 <OUTPUT2>
          Optional path to second paired output fastx file (detects .gz and .zst)
  -a, --abs-threshold <ABS_THRESHOLD>
          Minimum absolute number of minimizer hits for a match [default: 2]
  -r, --rel-threshold <REL_THRESHOLD>
          Minimum relative proportion (0.0-1.0) of minimizer hits for a match [default: 0.01]
  -p, --prefix-length <PREFIX_LENGTH>
          Search only the first N nucleotides per sequence (0 = entire sequence) [default: 0]
  -d, --deplete
          Discard matching sequences (invert filtering behaviour)
  -R, --rename
          Replace sequence headers with incrementing numbers
  -s, --summary <SUMMARY>
          Path to JSON summary output file
  -t, --threads <THREADS>
          Number of execution threads (0 = auto) [default: 8]
      --compression-level <COMPRESSION_LEVEL>
          Output compression level (1-9 for gz & xz; 1-22 for zstd) [default: 2]
      --debug
          Output sequences with minimizer hits to stderr
  -q, --quiet
          Suppress progress reporting
  -h, --help
          Print help

Indexing

$ deacon index -h
Create and compose minimizer indexes

Usage: deacon index <COMMAND>

Commands:
  build  Index minimizers contained within a fastx file
  info   Show index information
  union  Combine multiple minimizer indexes (A ∪ B…)
  diff   Subtract minimizers in one index from another (A - B)
  help   Print this message or the help of the given subcommand(s)

Options:
  -h, --help  Print help
$ deacon index build -h
Index minimizers contained within a fastx file

Usage: deacon index build [OPTIONS] <INPUT>

Arguments:
  <INPUT>  Path to input fastx file (supports gz, zst and xz compression)

Options:
  -k <KMER_LENGTH>
          K-mer length used for indexing (1-32) [default: 31]
  -w <WINDOW_SIZE>
          Minimizer window size used for indexing [default: 15]
  -o, --output <OUTPUT>
          Path to output file (- for stdout) [default: -]
  -c, --capacity <CAPACITY_MILLIONS>
          Preallocated index capacity in millions of minimizers [default: 400]
  -t, --threads <THREADS>
          Number of execution threads (0 = auto) [default: 8]
  -q, --quiet
          Suppress sequence header output
  -e, --entropy-threshold <ENTROPY_THRESHOLD>
          Minimum scaled entropy threshold for k-mer filtering (0.0-1.0)
  -h, --help
          Print help

Building custom indexes

Building custom Deacon indexes is quite fast. Nevertheless, when indexing many large genomes, it may be worthwhile separately indexing and subsequently combining indexes into one succinct index. Combine distinct minimizers from multiple indexes using deacon index union. Similarly, use deacon index diff to subtract the minimizers contained in one index from another. This can be helpful for e.g. eliminating shared minimizers between the target and host genomes when building custom (non-human) indexes for host depletion.

  • Use deacon index union 1.idx 2.idx 3.idx… > 1+2+3.idx to succinctly combine two (or more!) deacon indexes.
  • Use deacon index diff 1.idx 2.idx > 1-2.idx to subtract minimizers in 1.idx from 2.idx. Useful for masking out shared minimizer content between e.g. target and host genomes.
  • In version 0.7.0 and above, deacon index diff also supports subtracting minimizers from an index using a fastx file or stream, e.g. deacon index diff 1.idx 2.fa.gz > 1-2.idx or zcat *.fa.gz | deacon index diff 1.idx - > 1-2.idx.

For best performance, set the --capacity argument of deacon index build to a number of minimizers in millions greater than that you expect your index to contain. Setting this too low will cause delays during indexing for hash table resizing.

Filtering summary statistics

Use -s summary.json to save detailed filtering statistics:

{
  "version": "deacon 0.9.0",
  "index": "panhuman-1.k31w15.idx",
  "input": "HG02334.1m.fastq.gz",
  "input2": null,
  "output": "-",
  "output2": null,
  "k": 31,
  "w": 15,
  "abs_threshold": 2,
  "rel_threshold": 0.01,
  "prefix_length": 0,
  "deplete": true,
  "rename": false,
  "seqs_in": 1000000,
  "seqs_out": 13452,
  "seqs_removed": 986548,
  "seqs_removed_proportion": 0.986548,
  "bp_in": 5477122928,
  "bp_out": 5710050,
  "bp_removed": 5471412878,
  "bp_removed_proportion": 0.9989574727324798,
  "time": 125.755103875,
  "seqs_per_second": 7951,
  "bp_per_second": 43553881
}

Citation

biorXiv preprint

Bede Constantinides, John Lees, Derrick W Crook. "Deacon: fast sequence filtering and contaminant depletion" bioRxiv 2025.06.09.658732, https://doi.org/10.1101/2025.06.09.658732

Please also consider citing the SimdMinimizers paper:

Ragnar Groot Koerkamp, Igor Martayan. "SimdMinimizers: Computing random minimizers, fast" bioRxiv 2025.01.27.634998, https://doi.org/10.1101/2025.01.27.634998

Commit count: 154

cargo fmt