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3 results for “bowtie2”

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zenodo44/100

A termite genome reference and its Bowtie2 index

<p>This dataset contains a fasta file and its Bowtie2 index. The fasta file includes publicly available genomes of 5 termite species, namely <em>Zootermopsis nevadensis </em>(Terrapon, N., Li, C., Robertson, H. M., Ji, L., Meng, X., Booth, W., ... &amp; Liebig, J. (2014). Molecular traces of alternative social organization in a termite genome. Nature communications, 5(1), 1-12.), <em>Cryptotermes secundus</em> (Harrison, M. C., Jongepier, E., Robertson, H. M., Arning, N., Bitard-Feildel, T., Chao, H., ... &amp; Bornberg-Bauer, E. (2018). Hemimetabolous genomes reveal molecular basis of termite eusociality. Nature ecology &amp; evolution, 2(3), 557-566.), <em>Macrotermes natalensis</em> (Poulsen, M., Hu, H., Li, C., Chen, Z., Xu, L., Otani, S., ... &amp; Zhang, G. (2014). Complementary symbiont contributions to plant decomposition in a fungus-farming termite. Proceedings of the National Academy of Sciences, 111(40), 14500-14505.), <em>Coptotermes formosanus</em> (Draft genome sequence of the termite, Coptotermes formosanus: Genetic insights into the pyruvate dehydrogenase complex of the termite) and <em>Reticulitermes speratus </em>(Shigenobu, S., Hayashi, Y., Watanabe, D., Tokuda, G., Hojo, M. Y., Toga, K., Saiki, R., Yaguchi, H., Masuoka, Y., Suzuki, R., Suzuki, S., Kimura, M., Matsunami, M., Sugime, Y., Oguchi, K., Niimi, T., Gotoh, H., Hojo, M. K., Miyazaki, S., &hellip; Maekawa, K. (2022). Genomic and transcriptomic analyses of the subterranean termite Reticulitermes speratus: Gene duplication facilitates social evolution. Proceedings of the National Academy of Sciences, 119(3), e2110361119.). These genomic sequences have been classified with Kraken 2 v2.1.2 (Wood, D. E., Lu, J., &amp; Langmead, B. (2019). Improved metagenomic analysis with Kraken 2. Genome Biology, 20(1), 1&ndash;13 and Wood, D. E., &amp; Salzberg, S. L. (2014). Kraken: Ultrafast metagenomic sequence classification using exact alignments. Genome Biology, 15(3).) to remove all microbial sequences. This cleaned fasta file was indexed using the bowtie2-build command from Bowtie2 (Langmead, B., &amp; Salzberg, S. L. (2012). Fast gapped-read alignment with Bowtie 2. Nature Methods, 9(4), 357&ndash;359.) and can be used to perform &nbsp;alignments.</p>

opencc-by-4.0Jul 2022View details →
zenodo32/100

On taming the effect of transcript level intra-condition count variation during differential expression analysis: a story of dogs, foxes and wolves: Bowtie2 counts and kallisto abundances

<p>Intra [1] and inter [2-5] study RNA-seq read datasets representing the&nbsp;varying brain compartments&nbsp;of foxes (n=24), as well as dogs (n=14) and wolves (n=6), as described in Lobo <em>et al.</em>, (2022) (under review), were mapped&nbsp;to the dog reference transcriptome [6], which contained 26,107 annotated transcripts (Ensembl CanFam3.1, release 92) [7], using Bowtie2 v.2.3.4.1 [8] and using kallisto v0.46.1 [9]. Count data obtained following each mapping approach for each dataset had high correlations (Lobo <em>et al.</em>, Figure S2). Bowtie2 counts were subsequently used in multiple differential analysis experiments in order to explore the effects of intra-condition count variation on the detection of differentially expressed transcripts. The individual count and abundance datasets for each corresponding RNA-seq dataset are available here.</p> <p>&nbsp;</p> <p>A&nbsp;preprint of Lobo et al., 2022,&nbsp;currently under review for PLOS ONE, is available [10]. The preprint however&nbsp;does not contain reviewer requested information on simulations as this, along with other additions including an additional author RL,&nbsp;has been subsequently added during the review process. These additions will be made available following review via a link to the final paper.&nbsp;</p> <p>&nbsp;</p> <p>Related software to this project are:<br> 1.&nbsp;<a href="http://sourceforge.net/projects/cstone/">CStone</a>&nbsp;<br> 2.&nbsp;<a href="http://sourceforge.net/projects/csreadgen/">CSReadGen</a><br> 3.&nbsp;<a href="https://sourceforge.net/projects/cview/">CView</a>&nbsp;<br> 4.&nbsp;<a href="https://sourceforge.net/projects/chimsim/">ChimSim</a><br> 5.&nbsp;<a href="https://sourceforge.net/projects/tvscript/">TVScript</a>&nbsp;&lt;</p> <p>&nbsp;</p> <p>General details of the projects involved are available:&nbsp;<a href="https://cibio.up.pt/en/projects/is-hybridization-between-wolves-and-dogs-shaping-the-evolutionary-trajectory-of-wolf-populations-in-human-dominated-landscapes/">dog-wolf</a>&nbsp;and&nbsp;<a href="https://cibio.up.pt/en/projects/de-novo-based-sequence-assembly-of-next-generation-sequence-data-without-chimeras-improved-annotation-gene-expression-profiles-and-haplotype-br-reconstruction/">chimerism</a>.</p> <p>&nbsp;</p> <p><strong>References</strong></p> <p>1. Wang X, Pipes L, Trut L, Herbeck Y, Vladimirova A, Gulevich R, et al. Genomic responses to selection for tame/aggressive behaviors in the silver fox (Vulpes vulpes). Proc Natl Acad Sci. 2018;115: 10398&ndash;10403. doi:10.1073/pnas.1800889115</p> <p>&nbsp;</p> <p>2. Roy M, Kim N, Kim K, Chung WH, Achawanantakun R, Sun Y, et al. Analysis of the canine brain transcriptome with an emphasis on the hypothalamus and cerebral cortex. Mamm Genome. 2013;24: 484&ndash;499. doi:10.1007/s00335-013-9480-0</p> <p>&nbsp;</p> <p>3. Fushan AA, Turanov AA, Lee SG, Kim EB, Lobanov A V, Yim SH, et al. Gene expression defines natural changes in mammalian lifespan. Aging Cell. 2015;14: 352&ndash;365. doi:10.1111/acel.12283</p> <p>&nbsp;</p> <p>4. Hoeppner MP, Lundquist A, Pirun M, Meadows JRS, Zamani N, Johnson J, et al. An improved canine genome and a comprehensive catalogue of coding genes and non-coding transcripts. PLoS One. 2014;9(3):91172. doi:10.1371/journal.pone.0091172</p> <p>&nbsp;</p> <p>5. Albert FW, Somel M, Carneiro M, Aximu-Petri A, Halbwax M, Thalmann O, et al. A Comparison of Brain Gene Expression Levels in Domesticated and Wild Animals. Akey JM, editor. PLoS Genet. 2012;8:e1002962. doi:10.1371/journal.pgen.1002962</p> <p>&nbsp;</p> <p>6. Hoeppner MP, Lundquist A, Pirun M, Meadows JRS, Zamani N, Johnson J, et al. An improved canine genome and a comprehensive catalogue of coding genes and non-coding transcripts. PLoS One. 2014;9(3):91172. doi:10.1371/journal.pone.0091172</p> <p>&nbsp;</p> <p>7. Yates AD, Achuthan P, Akanni W, Allen J, Allen J, Alvarez-Jarreta J, et al. Ensembl 2020. Nucleic Acids Res. 2020;48: D682&ndash;D688. doi:10.1093/NAR/GKZ966</p> <p>&nbsp;</p> <p>8. Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. 2012. doi:10.1038/nmeth.1923</p> <p>&nbsp;</p> <p>9. Bray NL, Pimentel H, Melsted P, Pachter L. Near-optimal probabilistic RNA-seq quantification. Nat Biotechnol 2016 345. 2016;34: 525&ndash;527. doi:10.1038/nbt.3519</p> <p>&nbsp;</p> <p>10.&nbsp;Lobo D, Godinho R, Archer JP. On taming the effect of transcript level intra-condition count variation during differential expression analysis: a story of dogs, foxes and wolves. bioRxiv. 2022; 2022.01.24.477470. doi:10.1101/2022.01.24.477470</p>

opencc-by-4.0Jun 2022View details →
zenodo32/100

NOMAD element annotation bowtie2 indices

<p>Default list of bowtie2 annotations used in NOMAD manuscript</p>

opencc-by-4.0Jul 2022View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

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Last verified 2026-04-29Open record