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317 results for “gene structure”

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zenodo44/100

Simultaneous estimation of gene regulatory network structure and RNA kinetics from single cell gene expression

<p>Supplemental Data 1&nbsp;is single-cell response to rapamycin count data first sequenced in this work and deposited in GEO with accession GSE242556. It is a 173348 rows &times; 5847 columns TSV.GZ file where the first row is a header, the first 5843 columns are integer gene counts, and the final 4 columns (&#39;Gene&#39;, &#39;Replicate&#39;, &#39;Pool&#39;, and &#39;Experiment&#39;) are cell-specific metadata.</p> <p>Supplemental Data 2&nbsp;is bulk response to rapamycin count data first sequenced in this work. It is a 33 rows &times; 5847 columns TSV.GZ file where the first row is a header, the first 5843 columns are integer gene counts, and the final 4 columns (&#39;Oligo&#39;, &#39;Time&#39;, &#39;Replicate&#39;, and &#39;Sample_barcode&#39;) are sample-specific metadata.</p> <p>Supplemental Data 3 is single-cell count data published as GSE125162 and re-analyzed with the pipeline used for single-cell quantification in this work. It is a 65068 rows &times; 5850 columns TSV.GZ file where the first row is a header, the first 5843 columns are integer gene counts, and the final 7 columns (&#39;Condition&#39;, &#39;Sample&#39;, &#39;Genotype_Group&#39;, &#39;Genotype_Individual&#39;, &#39;Genotype&#39;, &#39;Replicate&#39;, &#39;Cell_Barcode&#39;) are cell-specific metadata.</p> <p>Supplemental Data 4&nbsp;is the four deep learning models trained in this work. It is a TAR.GZ file containing the final biophysical transcription/decay model, the pre-trained decay model, the velocity prediction model, and the count prediction model. Each model file is an h5 file containing a pytorch model that can be loaded with supirfactor\_dynamical.read().</p> <p>Supplemental Data 5&nbsp;is the prior knowledge network used to constrain the models for TF interpretability. It is a 1574 rows &times; 204 columns [Genes x TFs] TSV.GZ file where the first row is a header with TF names, the first column is an index of gene names, and TF-gene interactions are indicated by non-zero values in the matrix. There are 2799 TF-gene interactions.</p> <p><br> Supplemental Table 6 is the oligonucleotide sequences used in this work. It is a TSV file with a header row.</p> <p>Supplemental Table 7 is the yeast strains used in this work. It is a TSV file with a header row.</p> <p>Supplemental Table 8&nbsp;is gene metadata used in this work (e.g. Ribosomal Protein gene labels, etc). It is a TSV file with a header row.</p> <p>Supplemental Table 9&nbsp;is FY4/5 growth curve data generated in this work. It is a 20 rows &times; 7 columns TSV file where the first row is a header with replicate IDs, the first column is an index of times in minutes, and values are cell densities in YPD culture, in units of 10$^6$ cells / mL.</p> <p>Supplemental Data 10&nbsp;is a TAR.GZ file containing the yeast SacCer3 genome, modified to add UTR sequences, that was used to generate transcripts for kallisto pseudoalignment in this work.</p>

opencc-by-4.0Sep 2023View details →
zenodo40/100

Analyses of human cancer driver genes uncovers evolutionarily conserved RNA structural elements involved in posttranscriptional control - associated datasets

<p>These datasets include raw data output and associated files from ScanFold and CMbuilder analyses of human cancer driver gene mRNA. ScanFold was used to predict RNA regions of unusual thermodynamic stability, and CMbuilder was used to evaluate covariation&nbsp;of the predicted structures in those regions. Please view the&nbsp;file&nbsp;<em>README_general_description_Zenodo_files.txt</em>&nbsp;for brief descriptions of the content.</p> <p>These data are associated with the manuscript entitled&nbsp;<em>Analyses of human cancer driver genes uncovers evolutionarily conserved RNA structural elements involved in posttranscriptional control</em>. The manuscript has currently been submitted for review in PLOS ONE.</p>

opencc-by-4.0Sep 2021View details →
zenodo40/100

Fig. 9 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 9. Evolutionary hypothesis of interrelationships among the four free-living litostomatean lineages studied. This scenario was suggested on the basis of morphology and the consensus secondary structure of the ITS2 molecules. CK – circumoral kinety, DB – dorsal brush, OB – oral bulge, OO – oral bulge opening, P – proboscis, PE – perioral kinety, PR – preoral kineties, SK – somatic kineties.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 5 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 5. Quartet likelihood-mapping showing distribution of phylogenetic signal in the 18S-A and the CON-1 alignment for three possible relationships among the four main free-living litostomatean lineages studied. The corners of the triangles show the percentage of fully resolved trees, i.e., phylogenetically informative signal. The rectangular areas show the percentage of trees that are in conflict. The central triangle shows the percentage of unresolved star-like trees, i.e., phylogenetically uninformative signal. Coding of free-living litostomatean lineages: H – Haptorida, P – Pleurostomatida, R – Rhynchostomatia, S – Spathidiida.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 4 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 4. Super-network of 66 free-living litostomatean taxa constructed from 80 randomly selected post-burn-in trees from the Bayesian inference of the 18S-A–D, ITSR-C and ITSR-D as well as the CON-1 and CON-2 alignments. The super-network was constructed in the program SplitsTree, using the Z-closure option, tree size weighted mean, ten runs, and the refined heuristic technique. For details on taxa and characteristics of the alignments analyzed, see Supplementary Table S1 and S2.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 3 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 3. Phylogeny based on the 18S rRNA gene and the ITS1-5.8S-ITS2 region of 56 free-living litostomatean taxa (alignment CON-1). Posterior probabilities for the Bayesian inference and bootstrap values for maximum likelihood were mapped onto the 50% majority rule ML tree. Dashes indicate posterior probabilities below 0.50 and ML bootstrap values below 50%. The scale bar indicates five substitutions per ten nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the CON-1 alignment, see Supplementary Table S1 and S2.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 1 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 1. Phylogeny based on the 18S rRNA gene of 64 free-living litostomatean taxa (alignment 18S-A). Posterior probabilities for Bayesian inference and bootstrap values for maximum likelihood were mapped onto the 50% majority rule Bayesian consensus tree. Dashes indicate ML bootstrap values below 50%. Sequences in bold were obtained during this study. The scale bar indicates two substitutions per one hundred nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the 18S-A alignment, see Supplementary Table S1 and S2.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 8 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 8. Structure logo of ITS2 helices II and III in various higher litostomatean taxa. The height of a base is proportional to its frequency in multiple sequence alignments.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 2 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 2. Phylogeny based on the ITS1-5.8S-ITS2 region of 60 free-living litostomatean taxa (alignment ITSR-A). Posterior probabilities for Bayesian inference and bootstrap values for maximum likelihood were mapped onto the best ML tree. Dashes indicate posterior probabilities below 0.50 and ML bootstrap values below 50%. Sequences in bold were obtained during this study. The scale bar indicates nine substitutions per one hundred nucleotide positions. For details on taxa, evolutionary model used, and characteristics of the ITSR-A alignment, see Supplementary Table S1 and S2.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 7 in Constraints on Phylogenetic Interrelationships among Four Free-living Litostomatean Lineages Inferred from 18S rRNA gene-ITS Region sequences and Secondary Structure of the ITS2 molecule

Fig. 7. Consensus secondary structure of ITS2 helices II and III in various higher litostomatean taxa.

opencc-by-4.0Dec 2017View details →
zenodo40/100

Fig. 4 in Drainage Network Morphology Influences Population Structure and Gene Flow of the Andean Water Frog (Anura: Telmatobiidae) of the Atacama Desert, Northern Chile.

Fig. 4. Results of the Geneland analysis. A: Bar plot of posterior probability density according to the number of clusters; B: posterior probability maps for the delimited clusters.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 3 in Drainage Network Morphology Influences Population Structure and Gene Flow of the Andean Water Frog (Anura: Telmatobiidae) of the Atacama Desert, Northern Chile.

Fig. 3. Pairwise FST between localities of Telmatobius pefauri obtained using mitochondrial (A) and microsatellite (B) data. The colour scale corresponding to the values of FST is shown to the right of each matrix. Significant (Bonferroni corrected) comparisons showing p &lt;0.05, p &lt;0.01 and p &lt;0.001 are denoted by *, ** and ***, respectively.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 2 in Drainage Network Morphology Influences Population Structure and Gene Flow of the Andean Water Frog (Anura: Telmatobiidae) of the Atacama Desert, Northern Chile.

Fig. 2. Median-joining network based on the fragment of the analysed control region. Table 1. Indices of mitochondrial diversity, nuclear diversity, and inbreeding coefficients (FIS) by locality

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 1 in Drainage Network Morphology Influences Population Structure and Gene Flow of the Andean Water Frog (Anura: Telmatobiidae) of the Atacama Desert, Northern Chile.

Fig. 1. Study area, distribution of Telmatobius pefauri. Localities, 1: Socoroma (Socoroma River); 2: Murmuntani; 3: Copaquilla; 4: Chapiquiña; 5: Belén; 6: Lupica; 7: Saxamar. Localities 2 and 3 belong to the Seco River drainage; localities 4–7 belong to the Tignamar River drainage. Basin limits are indicated with dashed lines. The inset map shows the study area (highlighted by a red box) in relation to South America. SAAD = South American Arid Diagonal.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 5 in Drainage Network Morphology Influences Population Structure and Gene Flow of the Andean Water Frog (Anura: Telmatobiidae) of the Atacama Desert, Northern Chile.

Fig. 5. Scatter plot for the first two principal components obtained in the Principal Components Analysis using SSR data.

opencc-by-4.0Aug 2023View details →
zenodo40/100

Fig. 5 in The complete mitochondrial genome of Platygaster robiniae (Hymenoptera: Platygastridae): A novel tRNA secondary structure, gene rearrangements and phylogenetic implications

Fig. 5. Phylogenetic tree Note: (A): Maximum likelihood (ML) phylogenetic tree inferred from the mitochondrial genome based on the 13 PCGs dataset; (B): Bayesian inference (BI) phylogenetic tree inferred from the mitochondrial genome based on the 13 PCGs dataset.

opencc-by-4.0Aug 2022View details →
zenodo40/100

Fig. 4 in The complete mitochondrial genome of Platygaster robiniae (Hymenoptera: Platygastridae): A novel tRNA secondary structure, gene rearrangements and phylogenetic implications

Fig. 4. Mitochondrial genome organization of Platygaster robiniae and 11 species of Platygastroidea, compared with the ancestral pancrustacean mt genome organization. Note: tRNA genes are indicated by single letter amino acid codes, L1, L2, S1 and S2 denote tRNALeu(CUN), tRNALeu(UUR), tRNASer(AGN) and tRNASer(UCN), respectively. Genes are transcribed from left to right except those indicated by underlining. Gene movements, relative to the ancestral organization, are indicated with arrows.

opencc-by-4.0Aug 2022View details →
zenodo40/100

Fig. 2 in The complete mitochondrial genome of Platygaster robiniae (Hymenoptera: Platygastridae): A novel tRNA secondary structure, gene rearrangements and phylogenetic implications

Fig. 2. Amino acids (A) and relative synonymous codons (B) of protein-coding genes of the mitochondrial genome of Platygaster robiniae.

opencc-by-4.0Aug 2022View details →
zenodo40/100

Fig. 1 in The complete mitochondrial genome of Platygaster robiniae (Hymenoptera: Platygastridae): A novel tRNA secondary structure, gene rearrangements and phylogenetic implications

Fig. 1. Genetic map of the complete mitochondrial genome of Platygaster robiniae. Notes: the blue arrow represents the direction of gene transcription; the black peak represents the deviation of GC%; the purple and green peaks represent the deviation in GC skew; green refers to positive skew, and purple indicates negative skew. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2022View details →
zenodo40/100

Figure 2 in Phylogenetic structure of the Sphaeriinae, a global clade of freshwater bivalve molluscs, inferred from nuclear (ITS-1) and mitochondrial (16S) ribosomal gene sequences

Figure 2. Strict consensus of the 1040 equally most parsimonious trees (L = 445; CI = 0.724; RI = 0.886) obtained from the phylogenetic analysis of sphaeriid nuclear ITS1 rDNA sequences. The inferred evolutionary gain and loss of a ~160 nt fragment are indicated. Two Eupera species, E. cubensis and E. platensis, were designated as outgroups and inferred sequence gaps were considered as missing data. Numbers above the branches represent bootstrap values and numbers below indicate decay index values.

opencc-by-4.0Feb 2003View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record