align-trim 1.1.0__tar.gz

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+ name: Bug report
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+ attributes:
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+ label: Command used and terminal output
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+ description: Steps to reproduce the behaviour. Please paste the command you used to launch the pipeline and the output from your terminal.
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+ render: console
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+ placeholder: |
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+ $ align_trim ...
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+
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+ Some output where something broke
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+ label: Relevant files
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+ Please drag and drop the relevant files here. Create a `.zip` archive if the extension is not allowed.
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+ Your verbose log file (from stderr with --verbose enabled), the report TSV generated with `--report`, and your primer scheme bedfile are all helpful.
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+
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+ - type: textarea
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+ * Install method _(eg. pip, conda, source)_
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+ * Version of align_trim _(eg. 1.1, 1.5, 1.8.2)_
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+ name: Feature request
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+ description: Suggest an idea for the align_trim, please ensure you have checked existing feature requests before submitting a new suggestion to avoid duplicates.
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+ labels: enhancement
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+ python-version: ${{ matrix.python-version }}
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+ - name: install project
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+ run: uv sync --python ${{ matrix.python-version }} --locked --all-extras --dev
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+
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+ - name: run tests
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+ run: uv run --python ${{ matrix.python-version }} pytest
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+ packages-dir: dist/
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+ repos:
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+ - repo: https://github.com/astral-sh/ruff-pre-commit
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+ # Ruff version.
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+ rev: v0.4.1
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+ hooks:
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+ # Run the linter.
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+ - id: ruff
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+ args: [--fix, --show-fixes]
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+ # Run the formatter.
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+ - repo: https://github.com/astral-sh/uv-pre-commit
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+ # uv version.
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+ rev: 0.7.11
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+ hooks:
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+ - id: uv-lock
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+ - id: uv-export
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+ Copyright (c) 2017-2018 Nick Loman & the ZiBRA Project & the ARTIC project
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+
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+ Permission is hereby granted, free of charge, to any person obtaining a copy
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+ of this software and associated documentation files (the "Software"), to deal
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+ in the Software without restriction, including without limitation the rights
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+ to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
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+ copies of the Software, and to permit persons to whom the Software is
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+ furnished to do so, subject to the following conditions:
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+
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+ The above copyright notice and this permission notice shall be included in all
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+ copies or substantial portions of the Software.
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+
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+ THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
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+ IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
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+ FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE
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+ AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
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+ LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM,
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+ OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE
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+ SOFTWARE.
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+ Metadata-Version: 2.4
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+ Name: align_trim
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+ Version: 1.1.0
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+ Summary: Soft-clip primer sites for SAM/BAM files generated from amplicon sequencing runs
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+ Project-URL: Repository, https://github.com/artic-network/align_trim.git
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+ Project-URL: Issues, https://github.com/artic-network/align_trim/issues
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+ Author-email: Nick Loman <n.j.loman@bham.ac.uk>, Sam Wilkinson <s.a.j.wilkinson@bham.ac.uk>, Chris Kent <c.g.kent@bham.ac.uk>
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+ Maintainer-email: Sam Wilkinson <s.a.j.wilkinson@bham.ac.uk>, Chris Kent <c.g.kent@bham.ac.uk>
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+ License-Expression: MIT
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+ License-File: LICENSE
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+ Requires-Python: >=3.9
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+ Requires-Dist: numpy
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+ Requires-Dist: primalbedtools>=0.10.1
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+ Requires-Dist: pysam
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+ Description-Content-Type: text/markdown
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+
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+ # align_trim
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+
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+ Stand alone version of ARTIC's fieldbioinformatics align_trim.py
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+
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+ ## Installation
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+
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+ From conda
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+ ```bash
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+ conda install bioconda::align_trim
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+ ```
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+ from pypi
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+ ```bash
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+ pip install align_trim
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+ ```
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+ from source
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+ ```bash
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+ git clone https://github.com/artic-network/align_trim.git
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+ cd align_trim
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+ uv sync
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+ uv run align_trim --help
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+ ```
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+
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+ ## Command Line Interface
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+
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+ ### Basic Usage
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+
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+ ```bash
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+ align_trim [OPTIONS] BEDFILE
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+ ```
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+
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+ The tool reads alignment data from either a SAM/BAM file or stdin and outputs trimmed alignments to stdout in SAM format by default.
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+
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+ ### Required Arguments
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+
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+ - `BEDFILE`: BED file containing the amplicon primer scheme in [v3](https://doi.org/10.5281/zenodo.16366659) format.
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+
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+ ### Optional Arguments
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+
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+ #### Input/Output Options
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+
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+ - `--samfile`, `-s` : Sorted SAM/BAM file containing the aligned reads, if this is not provided (or '-') then 'align_trim' will read from stdin.
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+ - `--output`, `-o` : Output file path. Format determined by extension (.sam/.bam). If not provided or '-', writes SAM to stdout
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+
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+ #### Processing Options
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+
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+ - `--normalise`, `-n` : Normalise to target depth N per amplicon using a greedy per-read algorithm. Each read is kept only if it brings the amplicon depth closer to the target. Use 0 for no normalisation (default: 0)
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+ - `--min-mapq`, `-m` : Minimum mapping quality to keep an aligned read (default: 20)
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+ - `--primer-match-threshold`, `-p` : Add this many bases of padding to the 5' end of primer coordinates to allow fuzzy matching for reads with barcodes/adapters (default: 35)
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+
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+ #### Primer and Read Handling
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+
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+ - `--no-trim-primers` : Do not trim primers from reads (by default, primers are trimmed)
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+ - `--allow-incorrect-pairs` : Allow reads to be assigned to amplicons even if primers are not correctly paired
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+ - `--require-full-length` : Require all reads to start and stop in primer sites (do not use with rapid barcoding)
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+
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+ #### Output and Reporting
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+
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+ - `--report`, `-r` : Output detailed report TSV to specified filepath
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+ - `--amp-depth-report`, `-a` : Output mean depth for each amplicon as TSV to specified filepath
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+ - `--no-read-groups` : Do not divide reads into pool-based read groups in SAM/BAM output
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+
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+ #### General Options
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+
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+ - `--verbose`, `-v` : Enable debug mode with detailed logging to stderr
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+ - `--version` : Show version information
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+ - `--help` : Show help message
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+
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+ ### Examples
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+
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+ #### Basic trimming with primer removal
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --output trimmed.bam
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+ ```
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+
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+ #### Normalize coverage and generate reports
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --normalise 100 \
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+ --report alignment_report.tsv --amp-depth-report depth_report.tsv \
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+ --output normalized.bam
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+ ```
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+
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+ #### Process from stdin with verbose output
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+ ```bash
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+ samtools view -h input.bam | align_trim primers.bed --verbose > trimmed.sam 2> verbose.out.txt
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+ ```
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+
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+ #### Strict full-length read filtering
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --require-full-length \
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+ --min-mapq 30 --output filtered.bam
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+ ```
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+
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+ #### Allow mismatched primer pairs with custom threshold
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --allow-incorrect-pairs \
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+ --primer-match-threshold 50 --output relaxed.bam
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+ ```
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+
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+ ### Output Formats
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+
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+ The tool supports multiple output formats based on file extension:
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+ - `.sam` - SAM format (text)
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+ - `.bam` - BAM format (binary, compressed)
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+ - No extension or `-` - SAM format to stdout
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+
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+ ### Report Files
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+
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+ When using `--report`, a tab-separated file is generated with the following columns:
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+ - `chrom`: Reference chromosome/contig
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+ - `QueryName`: Read name
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+ - `ReferenceStart`/`ReferenceEnd`: Alignment coordinates
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+ - `PrimerPair`: Primer pair assignment
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+ - `Primer1`/`Primer2`: Individual primer information
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+ - `CorrectlyPaired`: Boolean indicating proper primer pairing
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+ - Additional alignment metrics
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+
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+ The `--amp-depth-report` generates a summary of coverage depth per amplicon.
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+ # align_trim
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+
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+ Stand alone version of ARTIC's fieldbioinformatics align_trim.py
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+
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+ ## Installation
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+
7
+ From conda
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+ ```bash
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+ conda install bioconda::align_trim
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+ ```
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+ from pypi
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+ ```bash
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+ pip install align_trim
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+ ```
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+ from source
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+ ```bash
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+ git clone https://github.com/artic-network/align_trim.git
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+ cd align_trim
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+ uv sync
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+ uv run align_trim --help
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+ ```
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+
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+ ## Command Line Interface
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+
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+ ### Basic Usage
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+
27
+ ```bash
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+ align_trim [OPTIONS] BEDFILE
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+ ```
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+
31
+ The tool reads alignment data from either a SAM/BAM file or stdin and outputs trimmed alignments to stdout in SAM format by default.
32
+
33
+ ### Required Arguments
34
+
35
+ - `BEDFILE`: BED file containing the amplicon primer scheme in [v3](https://doi.org/10.5281/zenodo.16366659) format.
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+
37
+ ### Optional Arguments
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+
39
+ #### Input/Output Options
40
+
41
+ - `--samfile`, `-s` : Sorted SAM/BAM file containing the aligned reads, if this is not provided (or '-') then 'align_trim' will read from stdin.
42
+ - `--output`, `-o` : Output file path. Format determined by extension (.sam/.bam). If not provided or '-', writes SAM to stdout
43
+
44
+ #### Processing Options
45
+
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+ - `--normalise`, `-n` : Normalise to target depth N per amplicon using a greedy per-read algorithm. Each read is kept only if it brings the amplicon depth closer to the target. Use 0 for no normalisation (default: 0)
47
+ - `--min-mapq`, `-m` : Minimum mapping quality to keep an aligned read (default: 20)
48
+ - `--primer-match-threshold`, `-p` : Add this many bases of padding to the 5' end of primer coordinates to allow fuzzy matching for reads with barcodes/adapters (default: 35)
49
+
50
+ #### Primer and Read Handling
51
+
52
+ - `--no-trim-primers` : Do not trim primers from reads (by default, primers are trimmed)
53
+ - `--allow-incorrect-pairs` : Allow reads to be assigned to amplicons even if primers are not correctly paired
54
+ - `--require-full-length` : Require all reads to start and stop in primer sites (do not use with rapid barcoding)
55
+
56
+ #### Output and Reporting
57
+
58
+ - `--report`, `-r` : Output detailed report TSV to specified filepath
59
+ - `--amp-depth-report`, `-a` : Output mean depth for each amplicon as TSV to specified filepath
60
+ - `--no-read-groups` : Do not divide reads into pool-based read groups in SAM/BAM output
61
+
62
+ #### General Options
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+
64
+ - `--verbose`, `-v` : Enable debug mode with detailed logging to stderr
65
+ - `--version` : Show version information
66
+ - `--help` : Show help message
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+
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+ ### Examples
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+
70
+ #### Basic trimming with primer removal
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --output trimmed.bam
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+ ```
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+
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+ #### Normalize coverage and generate reports
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --normalise 100 \
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+ --report alignment_report.tsv --amp-depth-report depth_report.tsv \
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+ --output normalized.bam
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+ ```
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+
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+ #### Process from stdin with verbose output
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+ ```bash
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+ samtools view -h input.bam | align_trim primers.bed --verbose > trimmed.sam 2> verbose.out.txt
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+ ```
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+
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+ #### Strict full-length read filtering
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --require-full-length \
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+ --min-mapq 30 --output filtered.bam
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+ ```
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+
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+ #### Allow mismatched primer pairs with custom threshold
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+ ```bash
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+ align_trim primers.bed --samfile input.bam --allow-incorrect-pairs \
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+ --primer-match-threshold 50 --output relaxed.bam
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+ ```
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+
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+ ### Output Formats
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+
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+ The tool supports multiple output formats based on file extension:
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+ - `.sam` - SAM format (text)
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+ - `.bam` - BAM format (binary, compressed)
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+ - No extension or `-` - SAM format to stdout
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+
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+ ### Report Files
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+
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+ When using `--report`, a tab-separated file is generated with the following columns:
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+ - `chrom`: Reference chromosome/contig
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+ - `QueryName`: Read name
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+ - `ReferenceStart`/`ReferenceEnd`: Alignment coordinates
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+ - `PrimerPair`: Primer pair assignment
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+ - `Primer1`/`Primer2`: Individual primer information
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+ - `CorrectlyPaired`: Boolean indicating proper primer pairing
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+ - Additional alignment metrics
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+
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+ The `--amp-depth-report` generates a summary of coverage depth per amplicon.
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