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software_references_mqc.yaml 7.05 KiB
id: 'software_references'
section_name: 'Software References'
description: 'This section describes references for the tools used.'
plot_type: 'html'
data: |
<h3 id="references">References</h3>
<ol style="list-style-type: decimal">
<li><strong>python</strong>:</li>
</ol>
<ul>
<li>Anaconda (Anaconda Software Distribution, <a href="https://anaconda.com" class="uri">https://anaconda.com</a>)</li>
</ul>
<ol start="2" style="list-style-type: decimal">
<li><strong>DERIVA</strong>:</li>
</ol>
<ul>
<li>Bugacov, A., Czajkowski, K., Kesselman, C., Kumar, A., Schuler, R. E., & Tangmunarunkit, H. (2017, October). Experiences with DERIVA: An asset management platform for accelerating eScience. In 2017 IEEE 13th International Conference on e-Science (e-Science) (pp. 79-88). IEEE. doi:<a href="https://doi.org/10.1109/eScience.2017.20">10.1109/eScience.2017.20</a>.</li>
</ul>
<ol start="3" style="list-style-type: decimal">
<li><strong>BDBag</strong>:<br />
</li>
</ol>
<ul>
<li>Madduri, R., Chard, K., DArcy, M., Jung, S. C., Rodriguez, A., Sulakhe, D., ... & Foster, I. (2019). Reproducible big data science: A case study in continuous FAIRness. PloS one, 14(4), e0213013. doi:<a href="https://doi.org/10.1371/journal.pone.0213013">10.1371/journal.pone.0213013</a>.</li>
</ul>
<ol start="4" style="list-style-type: decimal">
<li><strong>trimgalore</strong>:</li>
</ol>
<ul>
<li>trimgalore <a href="https://github.com/FelixKrueger/TrimGalore" class="uri">https://github.com/FelixKrueger/TrimGalore</a></li>
</ul>
<ol start="5" style="list-style-type: decimal">
<li><strong>hisat2</strong>:</li>
</ol>
<ul>
<li>Kim, D., Paggi, J. M., Park, C., Bennett, C., & Salzberg, S. L. (2019). Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. Nature biotechnology, 37(8), 907-915. doi:<a href="https://doi.org/10.1038/s41587-019-0201-4">10.1038/s41587-019-0201-4</a>.</li>
</ul>
<ol start="6" style="list-style-type: decimal">
<li><strong>samtools</strong>:</li>
</ol>
<ul>
<li>Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., ... & Durbin, R. (2009). The sequence alignment/map format and SAMtools. Bioinformatics, 25(16), 2078-2079. doi:<a href="http://dx.doi.org/10.1093/bioinformatics/btp352">10.1093/bioinformatics/btp352</a></li>
</ul>
<ol start="7" style="list-style-type: decimal">
<li><strong>picard</strong>:</li>
</ol>
<ul>
<li>“Picard Toolkit.” 2019. Broad Institute, GitHub Repository. <a href="http://broadinstitute.github.io/picard/" class="uri">http://broadinstitute.github.io/picard/</a>; Broad Institute</li>
</ul>
<ol start="8" style="list-style-type: decimal">
<li><strong>featureCounts</strong>:</li>
</ol>
<ul>
<li>Liao, Y., Smyth, G. K., & Shi, W. (2014). featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics, 30(7), 923-930. doi:<a href="https://doi.org/10.1093/bioinformatics/btt656">10.1093/bioinformatics/btt656</a>.</li>
</ul>
<ol start="9" style="list-style-type: decimal">
<li><strong>deeptools</strong>:</li>
</ol>
<ul>
<li>Ramírez, F., Ryan, D. P., Grüning, B., Bhardwaj, V., Kilpert, F., Richter, A. S., ... & Manke, T. (2016). deepTools2: a next generation web server for deep-sequencing data analysis. Nucleic acids research, 44(W1), W160-W165. doi:<a href="http://dx.doi.org/10.1093/nar/gkw257">10.1093/nar/gkw257</a></li>
</ul>
<ol start="10" style="list-style-type: decimal">
<li><strong>Seqtk</strong>:</li>
</ol>
<ul>
<li>Seqtk <a href="https://github.com/lh3/seqtk" class="uri">https://github.com/lh3/seqtk</a></li>
</ul>
<ol start="11" style="list-style-type: decimal"> <li><strong>R</strong>:</li>
</ol>
<ul>
<li>R Core Team 2014. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL:<a href="http://www.R-project.org/" class="uri">http://www.R-project.org/</a>.</li>
</ul>
<ol start="12" style="list-style-type: decimal">
<li><strong>FastQC</strong></li>
</ol>
<ul>
<li>FastQC <a href="https://www.bioinformatics.babraham.ac.uk/projects/fastqc/" class="uri">https://www.bioinformatics.babraham.ac.uk/projects/fastqc/</a></li>
</ul>
<ol start="13" style="list-style-type: decimal">
<li><strong>SeqWho</strong></li>
</ol>
<ul>
<li>Bennett, C., Thornton, M., Park, C., Henry, G., Zhang, Y., Malladi, V. S., & Kim, D. (2021). SeqWho: Reliable, rapid determination of sequence file identity using k-mer frequencies. bioRxiv, 2021.2003.2010.434827. doi:<a href="https://doi.org/10.1101/2021.03.10.434827">10.1101/2021.03.10.434827</a></li>
</ul>
<ol start="14" style="list-style-type: decimal">
<li><strong>RSeQC</strong>:</li>
</ol>
<ul>
<li>Wang, L., Wang, S., Li, W. 2012 RSeQC: quality control of RNA-seq experiments. Bioinformatics. Aug 15;28(16):2184-5. doi:<a href="https://doi.org/10.1093/bioinformatics/bts356">10.1093/bioinformatics/bts356</a>.</li>
</ul>
<ol start="15" style="list-style-type: decimal">
<li><strong>MultiQC</strong>:</li>
</ol>
<ul>
<li>Ewels, P., Magnusson, M., Lundin, S., & Käller, M. (2016). MultiQC: summarize analysis results for multiple tools and samples in a single report. Bioinformatics, 32(19), 3047-3048. doi:<a href="https://dx.doi.org/10.1093/bioinformatics/btw354">10.1093/bioinformatics/btw354</a></li>
</ul>
<ol start="16" style="list-style-type: decimal">
<li><strong>Nextflow</strong>:</li>
</ol>
<ul>
<li>Di Tommaso, P., Chatzou, M., Floden, E. W., Barja, P. P., Palumbo, E., & Notredame, C. (2017). Nextflow enables reproducible computational workflows. Nature biotechnology, 35(4), 316-319.</li>
</ul>