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8 results for “IGV”

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zenodo44/100

Schistosoma mansoni ATAC-seq results for IGV (female and male worms with and without LSD1 inhibitor)

<p>In this study, the anti-schistosomal activity of 39&nbsp;<em>Homo sapiens</em>&nbsp;Lysine Specific Demethylase 1 (HsLSD1) inhibitors was investigated on parasitic life cycle stages associated with both definitive and intermediate host infection. Amongst this collection of small molecules, compound&nbsp;<strong>33</strong>&nbsp;was the most potent and reduced&nbsp;<em>ex vivo</em>&nbsp;viabilities of schistosomula, juveniles, miracidia and adults. At its sub-lethal concentration to adults (3.13 &micro;M), compound&nbsp;<strong>33&nbsp;</strong>also significantly impacted oviposition, ovarian as well as vitellarian architecture and gonadal/neoblast stem cell proliferation. ATAC-seq analysis of adults demonstrated that compound&nbsp;<strong>33</strong>&nbsp;significantly affected chromatin structure (intragenic regions &gt; intergenic regions), especially in genes differentially expressed in cell populations (e.g., germinal stem cells, hes2<em><sup>+</sup></em>stem cell progeny, S1 cells and late female germinal cells) linked to these&nbsp;<em>ex vivo</em>&nbsp;phenotypes.</p> <p>The data presented here allow for visualisation in IGV&nbsp;https://igv.org/app/</p> <p>Produced in collaboration with IHPE.&nbsp;</p>

opencc-by-4.0Sep 2022View details →
zenodo44/100

IGV Bundle for Rhizophagus irregularis DAOM-197198

<p>Use these files to build&nbsp;your own genome browser for the &quot;Rhiir3&quot;&nbsp;<em>Rhizophagus&nbsp;irregularis</em> DAOM-197198 chromosome-scale genome assembly (PRJNA885267). Tracks available:</p> <p><strong>Gene annotation, based on Illumina and Nanopore RNA-Seq reads. </strong><br> Gene models were&nbsp;curated by excluding&nbsp;genes with InterPro domains related to&nbsp;transposable elements.<br> File: Rhiir3_PRJNA885267_genes.gff3</p> <p><strong>Repeat annotation. </strong><br> The repeat library was made using EDTA (Ou et al., 2019), and&nbsp;curated by excluding consensus sequences with InterPro domains of&nbsp;known cellular&nbsp;genes. Repeats were then masked using RepeatMasker&nbsp;(parameters&nbsp;-s -no_is -norna -nolow -div 40)&nbsp;(Smit et al., 2015).&nbsp;Unclassified repeats are grey-coloured and repeats classified into transposable elements categories are&nbsp;colour-coded: LINEs are blue, DNA transposons are pink and LTRs are green.<br> File: Rhiir3_PRJNA885267_repeats.gff3</p> <p><strong>Highly methylated CG sites,&nbsp;called via direct Nanopore genomic DNA sequencing of&nbsp;<em>R. irregularis </em>spores.<em>&nbsp;</em></strong><br> 161Gb of raw FAST5 files obtained from three R9.4.1 Nanopore flow cells were basecalled with Guppy5, producing 985,449 reads which were successfully processed by tombo&nbsp;(Stoiber et al., 2017)&nbsp;and used by DeepSignal2&nbsp;(Ni et al., 2019)&nbsp;to extract CG motifs and to call 5mC modifications using a human model (model.dp2.CG.R9.4_1D.human_hx1.bn17_sn16.both_bilstm.b17_s16_epoch4.ckpt.&nbsp;Only CG sites with &gt;80% 5mC are shown, and the track indicates&nbsp;methylation ratios measured as a fraction of 1 (0.80 to 1.00).<br> File: Rhiir3_PRJNA885267_high_meth_CG.bed</p> <p><strong>Index for CG methylation sites.</strong><br> File: Rhiir3_PRJNA885267_high_meth_CG.bed.idx</p> <p><strong>Nanopore RNA-Sequencing reads,&nbsp;poly(A)+ cDNA-PCR, from&nbsp;<em>R. irregularis</em> spores. </strong><br> Reads were trimmed of adapters and cleaned with seqclean to remove&nbsp;a&nbsp;percentage of undetermined bases,&nbsp;polyA tails,&nbsp;overall low complexity sequences and&nbsp;short terminal matches. Cleaned sequences were then mapped using minimap2 (options: -G&nbsp;max intron length=3000,&nbsp;-ax,&nbsp;map-ont).<br> File: Rhiir3_PRJNA885267_nano_cDNA.bam</p> <p><strong>Index for Nanopore RNA-Sequencing reads.</strong><br> File: Rhiir3_PRJNA885267_nano_cDNA.bam.bai</p> <p><strong>Small RNA loci.</strong><br> 70,956,710 small RNA-Seq reads from two replicates of oxidised and two replicates of column-purified spore RNA&nbsp;(Dallaire et al., 2021) were used to run ShortStack&nbsp;(Axtell, 2013)&nbsp;(parameters --dicermin 20 --dicermax 27 --foldsize 300 --pad 200 --mincov 10.0rpm --strand_cutoff 0.8 --mmap r).<br> File: Rhiir3_PRJNA885267_small_RNA_loci.gff3</p> <p><strong>Small RNA sequencing reads.</strong><br> Shortstack small RNA-Seq&nbsp;alignments,&nbsp;with multi-mappers randomly distributed.<br> File: Rhiir3_PRJNA885267_small_RNA.bam<br> <br> <strong>Index for small RNA sequencing reads.</strong><br> File: Rhiir3_PRJNA885267_small_RNA.bam.bai</p>

opencc-by-4.0Oct 2022View details →
zenodo36/100

Raw data of RNA-seq and IGV -2

<p>Raw data of RNA-seq and IGV of infected samples and mock infected samples</p>

opencc-by-4.0Oct 2019View details →
ClinicalTrials.gov32/100

EUS-guided Combined Therapy Versus Beta Blocker Therapy in Primary Prophylaxis o GOV II and IGV I

ClinicalTrials.gov study NCT04075760. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
zenodo28/100

IGV-results of Bowtie mapping

<p>&nbsp;Visualize sequence read alignment data.</p>

opencc-by-4.0Feb 2020View details →
zenodo28/100

IGV screenshot for manual validation of 60 reported false positive small CNVs in SurVIndel2

Open the record for dataset details and reuse information.

opencc-by-4.0Mar 2024View details →
zenodo24/100

Raw data of RNA-seq and IGV -1

<p>The raw data of&nbsp; RNA-seq and IGV data of infected samples and bacterial samples.</p>

opencc-by-4.0Oct 2019View details →
zenodo24/100

Supplementary IGV data for Human Embryonic RNA Editome

<p>Supplementary IGV data for Human Embryonic RNA Editome</p>

opencc-by-nc-nd-4.0Nov 2022View details →

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