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Merge pull request #185 from Plant-Food-Research-Open/patch/184
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Patched 183,184,179,178 for 2.2.1
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GallVp authored Dec 11, 2024
2 parents 0141925 + 0439cbf commit 39eb040
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2 changes: 1 addition & 1 deletion .nf-core.yml
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Expand Up @@ -46,5 +46,5 @@ template:
- igenomes
- multiqc
- fastqc
version: 2.2.0dev
version: 2.2.1
update: null
19 changes: 19 additions & 0 deletions CHANGELOG.md
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Expand Up @@ -3,6 +3,25 @@
The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)
and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).

## v2.2.1 - [11-Dec-2024]

### `Added`

1. Added notes on HTTP(s) server on the HiC page and on the need to move dynamically loaded content when moving the report's HTML file [#183](https://github.com/Plant-Food-Research-Open/assemblyqc/issues/183)

### `Fixed`

1. Fixed an issue where PLOTSR crashed due to a mismatch in the ordering of `syri.out` files when `synteny_plotsr_assembly_order` was not specified [#184](https://github.com/Plant-Food-Research-Open/assemblyqc/issues/184)
2. Fixed an issue where a path to HiC FastQ file pairs from the current directory were considered a SRR ID [#179](https://github.com/Plant-Food-Research-Open/assemblyqc/issues/179)
3. Fixed edges and input/output arrows in the flowchart [#178](https://github.com/Plant-Food-Research-Open/assemblyqc/issues/178)

### `Dependencies`

1. Nextflow!>=24.04.2
2. nf-schema@2.1.1

### `Deprecated`

## v2.2.0 - [05-Nov-2024]

### `Added`
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2 changes: 1 addition & 1 deletion CITATION.cff
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Expand Up @@ -25,7 +25,7 @@ authors:
- family-names: "Deng"
given-names: "Cecilia"
title: "AssemblyQC: A Nextflow pipeline for reproducible reporting of assembly quality"
version: 2.2.0
version: 2.2.1
date-released: 2024-07-30
url: "https://github.com/Plant-Food-Research-Open/assemblyqc"
doi: 10.1093/bioinformatics/btae477
7 changes: 5 additions & 2 deletions bin/report_modules/parsers/synteny_parser.py
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Expand Up @@ -147,9 +147,12 @@ def parse_synteny_plotsr(folder_name="synteny_outputs"):
"error_message": (
None
if error_comparisons == []
else "<b>Note:</b> Syri failed to detect structural rearrangements for following comparisons: "
else '<b style="color: red;">Error:</b> Syri failed to detect structural rearrangements for following comparisons: '
+ ", ".join(
[f"{target} with reference to {ref}" for (target, ref) in error_comparisons]
[
f"{target} with reference to {ref}"
for (target, ref) in error_comparisons
]
)
+ '. This may be due to known Syri limitations. See: <a href="https://github.com/schneebergerlab/syri/tree/ebd0f832e0df33398306f1b65f86801090c1ed49#current-limitations" target="_blank">GitHub/Syri/Limitations</a>'
),
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1 change: 1 addition & 0 deletions bin/report_modules/templates/header.html
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Expand Up @@ -136,6 +136,7 @@
width: 90%;
min-width: 700px;
margin: auto;
padding-bottom: 16px;
}

.dropdown select {
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31 changes: 25 additions & 6 deletions bin/report_modules/templates/hic/hic.html
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Expand Up @@ -8,38 +8,57 @@
<p class="section-para"><b>References:</b></p>

<p class="section-para">
<b>fastp</b> Chen, Yanqing Zhou, Yaru Chen, Jia Gu, fastp: an ultra-fast all-in-one FASTQ preprocessor, Bioinformatics,
<b>fastp</b> Chen, Yanqing Zhou, Yaru Chen, Jia Gu, fastp: an ultra-fast all-in-one FASTQ preprocessor,
Bioinformatics,
Volume 34, Issue 17, September 2018, Pages i884–i890, <a href="https://doi.org/10.1093/bioinformatics/bty560"
target="_blank">10.1093/bioinformatics/bty560</a>
</p>

<p class="section-para">
<b>BWA</b> Li, H. (2013). Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv preprint <a
href="https://arxiv.org/abs/1303.3997" target="_blank">arXiv: 1303.3997</a>.
<b>BWA</b> Li, H. (2013). Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv
preprint <a href="https://arxiv.org/abs/1303.3997" target="_blank">arXiv: 1303.3997</a>.
</p>

<p class="section-para">
<b>SAMBLASTER</b> Gregory G. Faust, Ira M. Hall, SAMBLASTER: fast duplicate marking and structural variant read extraction,
<b>SAMBLASTER</b> Gregory G. Faust, Ira M. Hall, SAMBLASTER: fast duplicate marking and structural variant read
extraction,
Bioinformatics, Volume 30, Issue 17, September 2014, Pages 2503–2505, <a
href="https://doi.org/10.1093/bioinformatics/btu314" target="_blank">10.1093/bioinformatics/btu314</a>
</p>

<p class="section-para">
<b>SAMtools</b> Petr Danecek, James K Bonfield, Jennifer Liddle, John Marshall, Valeriu Ohan, Martin O Pollard, Andrew Whitwham,
<b>SAMtools</b> Petr Danecek, James K Bonfield, Jennifer Liddle, John Marshall, Valeriu Ohan, Martin O Pollard,
Andrew Whitwham,
Thomas Keane, Shane A McCarthy, Robert M Davies, Heng Li, Twelve years of SAMtools and BCFtools, GigaScience,
Volume
10, Issue 2, February 2021, giab008, <a href="https://doi.org/10.1093/gigascience/giab008"
target="_blank">10.1093/gigascience/giab008</a>
</p>

<p class="section-para">
<b>Juicebox.js</b> Robinson JT, Turner D, Durand NC, Thorvaldsdóttir H, Mesirov JP, Aiden EL. Juicebox.js Provides a
<b>Juicebox.js</b> Robinson JT, Turner D, Durand NC, Thorvaldsdóttir H, Mesirov JP, Aiden EL. Juicebox.js Provides
a
Cloud-Based Visualization System for Hi-C Data. Cell Syst. 2018 Feb 28;6(2):256-258.e1.
<a href="https://doi.org/10.1016/j.cels.2018.01.001" target="_blank">10.1016/j.cels.2018.01.001</a>. Epub
2018 Feb 7. PMID: 29428417; PMCID: PMC6047755.
</p>

<p class="section-para"><b>Version: {{ all_stats_dicts['VERSIONS']['JUICEBOX_JS'] }}</b></p>

<p class="section-para"><b>Notes:</b></p>
<ul>
<li>
The Hi-C contact map is only loaded when the report is opened through a HTTP(s) server and all the necessary
permissions are in place. The contact map '.hic' file is stored in the 'hic' folder under the output directory.
It can be visualized with <a href="https://github.com/aidenlab/Juicebox/wiki/Download">Juicebox</a>.
</li>
<li>
This report dynamically loads content from the 'hic' folder under the output directory including '*.hic',
'*.html', 'bedpe/' and 'hicqc/'. These files and folders should also be moved when moving the report's HTML
file.
</li>
</ul>
</div>

{% include 'hic/dropdown.html' %} {% include 'hic/report_contents.html' %}
</div>
29 changes: 17 additions & 12 deletions bin/report_modules/templates/kraken2/kraken2.html
Original file line number Diff line number Diff line change
@@ -1,14 +1,19 @@
<div id="KRAKEN2" class="tabcontent" style="display: none">
<div class="section-para-wrapper">
<p class="section-para">
Kraken2 assigns taxonomic labels to sequencing reads for metagenomics projects.
</p>
<p class="section-para"><b>Reference:</b></p>
<p class="section-para">
Wood, D.E., Lu, J. & Langmead, B. Improved metagenomic analysis with Kraken 2. Genome Biol 20, 257 (2019).
<a href="https://doi.org/10.1186/s13059-019-1891-0" target="_blank">10.1186/s13059-019-1891-0</a>
</p>
<p class="section-para"><b>Version: {{ all_stats_dicts['VERSIONS']['KRAKEN2']['kraken2'] }}</b></p>
</div>
{% include 'kraken2/dropdown.html' %} {% include 'kraken2/report_contents.html' %}
<div class="section-para-wrapper">
<p class="section-para">
Kraken2 assigns taxonomic labels to sequencing reads for metagenomics projects.
</p>
<p class="section-para"><b>Reference:</b></p>
<p class="section-para">
Wood, D.E., Lu, J. & Langmead, B. Improved metagenomic analysis with Kraken 2. Genome Biol 20, 257 (2019).
<a href="https://doi.org/10.1186/s13059-019-1891-0" target="_blank">10.1186/s13059-019-1891-0</a>
</p>
<p class="section-para"><b>Version: {{ all_stats_dicts['VERSIONS']['KRAKEN2']['kraken2'] }}</b></p>

<p class="section-para"><b>Note:</b></p>
<p class="section-para">This report dynamically loads '*.kraken2.krona.html' files from the 'kraken2' folder under
the output directory. These files should also be moved when moving the report's HTML file.</p>

</div>
{% include 'kraken2/dropdown.html' %} {% include 'kraken2/report_contents.html' %}
</div>
46 changes: 25 additions & 21 deletions bin/report_modules/templates/ncbi_fcs_gx/ncbi_fcs_gx.html
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@@ -1,23 +1,27 @@
<div id="NCBI_FCS_GX" class="tabcontent" style="display: none">
<div class="section-para-wrapper">
<p class="section-para">FCS-GX detects contamination from foreign organisms in genome sequences.</p>
<p class="section-para"><b>Reference:</b></p>
<p class="section-para">
Alexander Astashyn, Eric S Tvedte, Deacon Sweeney, Victor Sapojnikov, Nathan Bouk, Victor Joukov, Eyal
Mozes, Pooja K Strope, Pape M Sylla, Lukas Wagner, Shelby L Bidwell, Karen Clark, Emily W Davis, Brian
Smith-White, Wratko Hlavina, Kim D Pruitt, Valerie A Schneider, Terence D Murphy bioRxiv 2023.06.02.543519;
doi:
<a href="https://doi.org/10.1101/2023.06.02.543519" target="_blank">10.1101/2023.06.02.543519</a>, GitHub:
<a href="https://github.com/ncbi/fcs" target="_blank">https://github.com/ncbi/fcs</a>
</p>
<p class="section-para">
<b>Version: {{ all_stats_dicts['VERSIONS']['NCBI_FCS_GX_SCREEN_SAMPLES']['fcs_gx'] }}</b>
</p>
<p class="section-para">
<b>DB Version: {{ all_stats_dicts['NCBI_FCS_GX'][0]['report_meta_data'][1]['db']['build-date'] }}</b>
</p>
</div>
{% include 'ncbi_fcs_gx/dropdown.html' %}
{% include 'ncbi_fcs_gx/summary_contents.html' %}
{% include 'ncbi_fcs_gx/report_contents.html' %}
<div class="section-para-wrapper">
<p class="section-para">FCS-GX detects contamination from foreign organisms in genome sequences.</p>
<p class="section-para"><b>Reference:</b></p>
<p class="section-para">
Alexander Astashyn, Eric S Tvedte, Deacon Sweeney, Victor Sapojnikov, Nathan Bouk, Victor Joukov, Eyal
Mozes, Pooja K Strope, Pape M Sylla, Lukas Wagner, Shelby L Bidwell, Karen Clark, Emily W Davis, Brian
Smith-White, Wratko Hlavina, Kim D Pruitt, Valerie A Schneider, Terence D Murphy bioRxiv 2023.06.02.543519;
doi:
<a href="https://doi.org/10.1101/2023.06.02.543519" target="_blank">10.1101/2023.06.02.543519</a>, GitHub:
<a href="https://github.com/ncbi/fcs" target="_blank">https://github.com/ncbi/fcs</a>
</p>
<p class="section-para">
<b>Version: {{ all_stats_dicts['VERSIONS']['NCBI_FCS_GX_SCREEN_SAMPLES']['fcs_gx'] }}</b>
</p>
<p class="section-para">
<b>DB Version: {{ all_stats_dicts['NCBI_FCS_GX'][0]['report_meta_data'][1]['db']['build-date'] }}</b>
</p>

<p class="section-para"><b>Note:</b></p>
<p class="section-para">This report dynamically loads '*.fcs.gx.krona.html' files from the 'ncbi_fcs_gx' folder under the output
directory. These files should also be moved when moving the report's HTML file.</p>
</div>
{% include 'ncbi_fcs_gx/dropdown.html' %}
{% include 'ncbi_fcs_gx/summary_contents.html' %}
{% include 'ncbi_fcs_gx/report_contents.html' %}
</div>
77 changes: 40 additions & 37 deletions bin/report_modules/templates/synteny_circos/synteny_circos.html
Original file line number Diff line number Diff line change
@@ -1,39 +1,42 @@
<div id="SYNTENY_CIRCOS" class="tabcontent" style="display: none">
<div class="section-para-wrapper">
<p class="section-para">
Circos facilitates the identification and analysis of similarities and differences arising from comparisons
of genomes. The genome-wide alignments are performed with MUMMER.
</p>
<p class="section-para"><b>References:</b></p>
<p class="section-para">
Krzywinski, M., Schein, J., Birol, I., Connors, J., Gascoyne, R., Horsman, D., ... & Marra, M. A. (2009).
Circos: an information aesthetic for comparative genomics. Genome research, 19(9), 1639-1645.
<a href="https://doi.org/10.1101/gr.092759.109" target="_blank">10.1101/gr.092759.109</a>
</p>
<p class="section-para">
Marçais G, Delcher AL, Phillippy AM, Coston R, Salzberg SL, Zimin A. MUMmer4: A fast and versatile genome
alignment system. PLoS Comput Biol. 2018 Jan 26;14(1):e1005944.
<a href="https://doi.org/10.1371/journal.pcbi.1005944" target="_blank">10.1371/journal.pcbi.1005944</a>
</p>
<p class="section-para">
<b
>Versions: {{ all_stats_dicts['VERSIONS']['CIRCOS']['circos'] }} (CIRCOS), {{
all_stats_dicts['VERSIONS']['MUMMER']['nucmer'] }} (MUMMER)</b
>
</p>
<p class="section-para"><b>Notes:</b></p>
<ul>
<li>
Alignments within a distance of {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_max_gap'] }}bp have been
bundled together.
</li>
<li>
After bundling, any bundle smaller than {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_min_bundle_size'] }}bp has been filtered out.
</li>
<li>
The sequence labels shown on the plot are based on the labelling file provided to the pipeline. These labels may or may not be same as the sequence IDs in the corresponding FASTA files.
</li>
</ul>
</div>
{% include 'synteny_circos/dropdown.html' %} {% include 'synteny_circos/report_contents.html' %}
<div class="section-para-wrapper">
<p class="section-para">
Circos facilitates the identification and analysis of similarities and differences arising from comparisons
of genomes. The genome-wide alignments are performed with MUMMER.
</p>
<p class="section-para"><b>References:</b></p>
<p class="section-para">
Krzywinski, M., Schein, J., Birol, I., Connors, J., Gascoyne, R., Horsman, D., ... & Marra, M. A. (2009).
Circos: an information aesthetic for comparative genomics. Genome research, 19(9), 1639-1645.
<a href="https://doi.org/10.1101/gr.092759.109" target="_blank">10.1101/gr.092759.109</a>
</p>
<p class="section-para">
Marçais G, Delcher AL, Phillippy AM, Coston R, Salzberg SL, Zimin A. MUMmer4: A fast and versatile genome
alignment system. PLoS Comput Biol. 2018 Jan 26;14(1):e1005944.
<a href="https://doi.org/10.1371/journal.pcbi.1005944" target="_blank">10.1371/journal.pcbi.1005944</a>
</p>
<p class="section-para">
<b>Versions: {{ all_stats_dicts['VERSIONS']['CIRCOS']['circos'] }} (CIRCOS), {{
all_stats_dicts['VERSIONS']['MUMMER']['nucmer'] }} (MUMMER)</b>
</p>

<p class="section-para"><b>Notes:</b></p>
<ul>
<li>
Alignments within a distance of {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_max_gap'] }}bp have been
bundled together.
</li>
<li>
After bundling, any bundle smaller than {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_min_bundle_size'] }}bp
has been filtered out.
</li>
<li>
The sequence labels shown on the plot are based on the labelling file provided to the pipeline. These labels may
or may not be same as the sequence IDs in the corresponding FASTA files.
</li>
</ul>

</div>

{% include 'synteny_circos/dropdown.html' %} {% include 'synteny_circos/report_contents.html' %}
</div>
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Expand Up @@ -10,14 +10,16 @@
<p class="section-para">
<b>Version: {{ all_stats_dicts['VERSIONS']['MUMMER']['nucmer'] }} (MUMMER)</b>
</p>

<p class="section-para"><b>Notes:</b></p>
<ul>
<li>
Alignments within a distance of {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_max_gap'] }}bp have been
bundled together.
</li>
<li>
After bundling, any bundle smaller than {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_min_bundle_size'] }}bp has
After bundling, any bundle smaller than {{ all_stats_dicts['PARAMS_DICT']['synteny_mummer_min_bundle_size'] }}bp
has
been filtered out.
</li>
<li>
Expand All @@ -26,5 +28,6 @@
</li>
</ul>
</div>

{% include 'synteny_dotplot/dropdown.html' %} {% include 'synteny_dotplot/report_contents.html' %}
</div>
Original file line number Diff line number Diff line change
Expand Up @@ -31,6 +31,11 @@
all_stats_dicts['VERSIONS']['SYRI']['syri'] }} (SYRI), {{
all_stats_dicts['VERSIONS']['MINIMAP2_ALIGN']['minimap2'] }} (MINIMAP2)</b>
</p>

<p class="section-para"><b>Note:</b></p>
<p>This report dynamically loads '*.on.*.all/' folders from the 'synteny' folder under the output directory. These
folders should also be moved when moving the report's HTML file.</p>

</div>
{% include 'synteny_plotsr/report_contents.html' %}
</div>
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2 changes: 1 addition & 1 deletion nextflow.config
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Expand Up @@ -274,7 +274,7 @@ manifest {
description = """A Nextflow pipeline which evaluates assembly quality with multiple QC tools and presents the results in a unified html report."""
mainScript = 'main.nf'
nextflowVersion = '!>=24.04.2'
version = '2.2.0'
version = '2.2.1'
doi = 'https://doi.org/10.1093/bioinformatics/btae477'
}

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2 changes: 1 addition & 1 deletion subworkflows/local/fasta_synteny.nf
Original file line number Diff line number Diff line change
Expand Up @@ -344,7 +344,7 @@ workflow FASTA_SYNTENY {
| map { meta, syri, fastas ->
def fasta_list = fastas.flatten()
def syri_tags = syri.collect { it.name.replace('syri.out', '').split(/\.on\./).toList() }.flatten().unique()
def proposed_order = plotsr_assembly_order ? plotsr_assembly_order.tokenize(' ') : syri_tags.sort(false)
def proposed_order = plotsr_assembly_order ? plotsr_assembly_order.tokenize(' ') : syri_tags.sort(false) { it.toUpperCase() }

def available_tags = []
proposed_order.each { tag -> if ( tag in syri_tags ) available_tags << tag }
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