SequenceDot

SequenceDot is a command-line tool for generating k-mer based dotplots from biological sequences.

It supports DNA, RNA, and protein sequences and can compare sequences in forward, reverse-complement, or both directions.

Output example

SequenceDot can visualise both forward and reverse-complement sequence similarity. Forward matches appear as a diagonal, while reverse-complement matches appear as an anti-diagonal.

Plot generated with:

seqdot examples/seq1.fasta examples/seq2.fasta --kmer 7 --point-size 7 --strand both --output examples/example.png

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Features

FASTA and compressed FASTA support

SequenceDot accepts standard FASTA files (.fasta, .fa, .fna), as well as gzipped FASTA files (.fasta.gz) without requiring manual decompression

seqdot sequence1.fasta.gz sequence2.fasta.gz

This is also possible with multi-sequence FASTA files with --file

K-mer based sequence comparison

The default k-mer size is 11. Use --kmer to change value. Values between 1 and 100 are accepted.

For shorter sequences, a smaller k-mer size might be required. For longer sequences, larger k-mer values may provide more specific matches. The chosen k-mer size cannot be longer than the shortest sequence, when using --file with --all-vs-all.

DNA, RNA, and amino acid sequences

The default expectation is DNA sequences.

Sequences are converted to uppercase. K-mers containing ambiguous characters such as N (DNA/RNA) or X (protein) are ignored during matching.

Other supported alphabets are: RNA and AA (amino acid sequences)

For amino acid sequences, all valid amino acid characters are accepted.

Forward, reverse-complement, and dual-strand comparisons

The default is forward strand comparison.

Available options are: forward reverse both

Forward matches are shown along the main diagonal. Reverse-complement matches are shown along the anti-diagonal.

Coloured strand-aware dotplots

When using --strand both, forward and reverse-complement matches are shown as different colours on the same dotplot.

Adjustable dot size

The default dot size is 1.0.

The optimal dot size depends on sequence length and the desired plot resolution.

Values between 0.1 and 100 are accepted.

High-resolution output

The default output format is: dotplot.png

Supported output formats are: .png .pdf .svg

seqdot sequence1.fasta sequence2.fasta --output comparison.pdf

All-vs-all batch comparison

SequenceDot can compare each sequence in a multi-sequence FASTA file against all other sequences.

seqdot --file sequences.fasta --all-vs-all

Output plots are written to the output directory, together with summary .tsv file. Default directory is /seqdot_results/. Placed in directory where SequenceDot is run. This directory can be defined with --output-dir.

A progress bar is shown in the terminal by default. Can be turned off with --silent.

By default, self-comparisons are skipped. To include these, use --include-self.

Output file naming

As a default for single comparisons, the file name is based on the two input sequences.

sequence1_vs_sequence2.png

As a default for batch comparisons, a folder seqdot_results/ is created.

seqdot_results/
├── sequence1_vs_sequence2.png
├── sequence1_vs_sequence3.png
├── sequence2_vs_sequence3.png
└── comparisons.tsv

Both default settings can be altered in the command line with --output for single plots and --output-dir for folders.

Summary TSV file generation

A summary TSV file is automatically generated and placed in the output directory. Generated as part of batch comparison with --all-vs-all.

It contains one row per comparison:

sequence1	sequence2	matching_kmers
seq1	seq2	153
seq1	seq3	88

Parallel processing

When running --all-vs-all, SequenceDot can use multiple CPU cores.

To automatically use all available cores:

seqdot --file sequences.fasta --all-vs-all --threads auto

To specify the number of CPU cores:

seqdot --file sequences.fasta --all-vs-all --threads 4

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Installation

PyPI installation

pip install SequenceDot

Clone the repository

git clone https://github.com/MarliesJFrancine/SequenceDot.git
cd SequenceDot

Create and activate an environment

python3 -m venv .venv
source .venv/bin/activate

Install SequenceDot

pip install .

Developmental installation

For development, install SequenceDot in editable mode:

pip install -e .

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Web interface

A web interface is available at sequencedot-marliesjfrancine.streamlit.app

This option only supports single FASTA sequence comparisons (.fasta, .fa, .fna, or .gz) while still allowing adjustable parameters.

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Usage

Generate a dotplot from two sequence files:

seqdot sequence1.fasta sequence2.fasta

Default parameters:

--kmer = 11
--alphabet = DNA
--strand = forward
--point-size = 1
--output = dotplot.png

For all available options:

seqdot --help

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Input requirements

SequenceDot is designed for unaligned biological sequences.

Accepted input:

• FASTA files containing DNA, RNA, or amino acid (AA) sequences (.fasta, .fa, and .fna)
• One sequence per file (single comparison) or multiple sequences in a FASTA file (batch mode)
• Gzipped FASTA files (.fasta.gz)
• ZIP archives (.zip) are not supported and must be extracted before use

The following characters are handled as follows:

Character	Assumption	Behaviour
N (DNA/RNA)	Unknown nucleotide	k-mers containing N are ignored
X (protein)	Unknown amino acid	k-mers containing X are ignored
- (gap)	Alignment gap	SequenceDot will report an error because the input appears to be an alignment
Any other invalid character	Invalid sequence	SequenceDot will reprot an error because the input is not recognized as DNA, RNA, or AA

Gap characters (-) indicate an aligned sequence. SequenceDot compares raw sequences using k-mers and therefore does not accept aligned sequences containing gaps.

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Modify parameters

Change k-mer size

seqdot sequence1.fasta sequence2.fasta --kmer 21

Compare reverse-complement strands

seqdot sequence1.fasta sequence2.fasta --strand reverse

Compare both strands

seqdot sequence1.fasta sequence2.fasta --strand both

Compare amino acid sequences

seqdot sequence1.fasta sequence2.fasta --alphabet AA

Compare RNA sequences

seqdot sequence1.fasta sequence2.fasta --alphabet RNA

Change dot size

seqdot sequence1.fasta sequence2.fasta --point-size 5

Change output name and format

seqdot sequence1.fasta sequence2.fasta --output comparison.pdf

Save output in a directory

seqdot --file sequences.fasta --all-vs-all --output-dir plots/

Include self-comparisons

To include self-comparisons when plotting a multi-sequence FASTA file with --all-vs-all.

seqdot --file sequences.fasta --all-vs-all --include-self --output-dir plots/

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Run tests

SequenceDot uses pytest for automated testing.

pytest