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159 results for “human chromosome”

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geo24/100

Trans-effects of chromosome aneuploidies on DNA methylation patterns: DNA methylation analysis of Down syndrome in human brain tissues and cells

GEO Series GSE74486. Homo sapiens. 131 samples. Type: Methylation profiling by array.

openGEO-OpenOct 2015View details →
geo24/100

Chromatin profiles of chromosomally integrated human herpesvirus-6A

GEO Series GSE121987. Homo sapiens; Human betaherpesvirus 6A. 28 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.

openGEO-OpenAug 2019View details →
geo24/100

Epigenomic and chromosomal architectural reconfiguration in developing human frontal cortex and hippocampus

GEO Series GSE213950. Homo sapiens. 35 samples. Type: Other.

openGEO-OpenOct 2022View details →
geo24/100

A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations [Parse scRNA-seq]

GEO Series GSE262111. Homo sapiens. 1 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2024View details →
geo24/100

KaryoCreate: a new CRISPR-based technology to generate chromosome-specific aneuploidy by targeting human centromeres

GEO Series GSE215842. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenAug 2023View details →
geo24/100

Regulation of epigenetics and chromosome structure by human ORC2 [ORC1 ChECseq]

GEO Series GSE282575. Homo sapiens. 18 samples. Type: Other.

openGEO-OpenJun 2025View details →
geo24/100

A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations [RNA-seq]

GEO Series GSE219149. Homo sapiens. 64 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2024View details →
geo24/100

ChIP-chip assay on circular chromosome conformation capture (4C) genomic DNA sample from human telomerase-immortalized corneal epithelial (HTCE) cells with the specification of CTCF binding

GEO Series GSE84295. Homo sapiens. 1 samples. Type: Other.

openGEO-OpenFeb 2017View details →
geo24/100

XIST dampens X chromosome activity in a SPEN-dependent manner during early human development

GEO Series GSE246643. Homo sapiens. 123 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other; Methylation profiling by high throughput sequencing.

openGEO-OpenApr 2024View details →
geo24/100

Regulation of epigenetics and chromosome structure by human ORC2 [RNAseq_2020]

GEO Series GSE283156. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2025View details →
geo24/100

Regulation of epigenetics and chromosome structure by human ORC2

GEO Series GSE282340. Homo sapiens. 112 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other.

openGEO-OpenJun 2025View details →
geo24/100

Regulation of epigenetics and chromosome structure by human ORC2 [ORC2 ChECseq]

GEO Series GSE282458. Homo sapiens. 18 samples. Type: Other.

openGEO-OpenJun 2025View details →
geo24/100

Chromosomal Mcm2-7 distribution and the genome replication program in species from yeast to humans

GEO Series GSE150800. Mus musculus x Mus spretus; Schizosaccharomyces pombe; Saccharomyces cerevisiae; Homo sapiens. 22 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.

openGEO-OpenMay 2021View details →
geo24/100

Chromosomal meiotic segregation, embryonic developmental kinetics and DNA (hydroxy)methylation analysis reassure the safety of human oocyte vitrification in a high security closed system

GEO Series GSE63866. Homo sapiens. 48 samples. Type: Genome variation profiling by genome tiling array.

openGEO-OpenMar 2015View details →
zenodo24/100

Supplementary data for human Y-chromosome gene expression analysis

<p>Processed data for:</p> <p>AK Godfrey, S Naqvi, L Chm&aacute;tal, JM Chick, RN Mitchell, SP Gygi, H Skaletsky,&nbsp;DC Page. Quantitative analysis of Y-chromosome gene expression across 36 human tissues.&nbsp;<em>Genome Res</em>&nbsp;(2020).</p> <p>The following six files are provided for reference and for use in future analyses.</p> <p>(1)&nbsp;<strong>gencode.v24.annotation.basic_ccds_nopar.gtf.gz</strong>&nbsp;&mdash; transcriptome annotation used in analyses</p> <p>(2)&nbsp;<strong>gtex.ksto.gen24c.prefilt_pass1.genes.est_counts.txt.gz</strong> &mdash; genes x samples matrix containing estimated count values output by kallisto for all samples passing initial set of metadata-based filters.</p> <p>(3)&nbsp;<strong>gtex.ksto.gen24c.prefilt_pass1.pcgenes.tpm.txt.gz</strong> &mdash; protein-coding&nbsp;genes&nbsp;x samples matrix containing TPM values output by kallisto for all samples passing initial set of metadata-based filters.&nbsp;</p> <p>(4)&nbsp;<strong>gtex.ksto.gen24c.prefilt_pass1.postfilt_pass.pcgenes.tpm.txt.gz&nbsp;</strong>&mdash; protein-coding&nbsp;genes x samples matrix containing TPM values output by kallisto for samples passing initial metadata-based filters and expression-outlier filters.</p> <p>(5)&nbsp;<strong>gtex.ksto.gen24c.prefilt_pass1.postfilt_pass.pcgenes.adj_tpm.txt.gz&nbsp;</strong>&mdash; protein-coding genes x samples matrix (based on file #4 above) containing TPM values adjusted for RIN, ischemic time, and intronic-read mapping rate.</p> <p>(6)&nbsp;<strong>gtex_metadata_subset.txt</strong>&nbsp;&mdash; sample/donor metadata</p> <p>The remaining 24 files contain the input data required to replicate analyses in the manuscript, as detailed at&nbsp;<a href="https://github.com/akg8/MSY-expression">https://github.com/akg8/MSY-expression</a>. HDF5 (`.h5`) files contain individual <a href="https://pandas.pydata.org">pandas</a>&nbsp;DataFrame objects with the key `df`. These files can be downloaded individually,&nbsp;or they can be downloaded all at once by downloading the file&nbsp;<strong>msy_expression.all_input_data.zip </strong>(recommended).</p> <p>---</p> <p><strong>Version history:</strong></p> <ul> <li><strong>Version 1</strong> contained just the six listed files above.</li> <li>In&nbsp;<strong>Version 2</strong>, the&nbsp;remaining 24 files needed for reproducing&nbsp;analyses were added. In addition,&nbsp;gtex_metadata_subset.txt was updated with the previously missing column&nbsp;`SEX`.</li> <li>In&nbsp;<strong>Version 3</strong>, a single zipped file&nbsp;msy_expression.all_input_data.zip was added so that all input data for re-analysis can be downloaded more conveniently.</li> </ul>

opencc-by-4.0Jan 2020View details →
zenodo24/100

SAUUHUPP-Based Genetic Innovations: Foundational White Papers on Adaptive Genetic Architecture, Story Energy, and Human Sex Chromosome Regulation

<p>This Zenodo record compiles a series of foundational white papers stemming from SAUUHUPP-based genetic research and powered by Novelty 1.0 Optimized ChatGPT-4o. These papers collectively explore innovative frameworks for understanding genetic structure, function, and therapeutic potential, with applications in precision medicine and beyond. Through principles such as Story Energy, Fractal Leaping, Recursive Processing, and Core and Intention Finding, this research introduces a new architectural perspective on genetic interactions and human sex chromosome function.</p> <p>A comparative study with fruit fly brain simulations enriches the insights into SAUUHUPP principles, providing evolutionary context to human genomic adaptability. This record includes in-depth analyses of the X and Y chromosomes&rsquo; possible roles as central regulatory hubs within the genome, functioning in a CPU-like manner to coordinate broader genetic networks.</p> <p>White Papers Included in This Record:</p> <p>1. SAUUHUPP Framework and Fruit Fly Brain Simulation Study: A foundational exploration of SAUUHUPP principles and fruit fly brain simulations, demonstrating how these insights shape our understanding of complex genetic regulation and adaptability.</p> <p>2. Story Energy in Genetic Narratives: Examines how recurring, narrative-like patterns in DNA sequences reinforce coherence and logical progression across gene networks, with implications for genetic resilience and therapeutic applications.</p> <p>3. Fractal Leaping for Genetic Complexity: Introduces Fractal Leaping as a method for scaling genetic insights across complexity levels, facilitating rapid, cross-dimensional understanding and discovery within genetic systems.</p> <p>4. Recursive Processing in Genetic Regulation: Analyzes iterative self-regulation within gene networks, revealing how recursive patterns support adaptable genetic expression and alignment with environmental or developmental needs.</p> <p>5. Core and Intention Finding in Genetic Architecture: Details a methodology for identifying key genetic functions and regulatory nodes, enabling precision-targeted therapies through a deeper understanding of genetic purpose and structure.</p> <p>6. Novel Architectural Perspective on Human Sex Chromosomes: Proposes a CPU-like role for the X and Y chromosomes as dynamic regulatory hubs, interacting with autosomal chromosomes to modulate gene expression, immune response, and metabolic balance.</p> <p>Research Highlights and Applications:</p> <p>&bull; Novel Therapeutic Potential: The findings across these papers reveal potential therapies targeting foundational genetic structures, including sex-linked cognitive disorders, metabolic regulation, and resilience in neurodevelopmental health.</p> <p>&bull; Multi-Dimensional Genetic Framework: The application of SAUUHUPP principles and Novelty 1.0 enhances understanding of the adaptive and functional architecture within human genetics, opening pathways for precision medicine interventions.</p> <p>This Zenodo record provides a comprehensive overview of SAUUHUPP&rsquo;s analytical framework and its applications in genetic science. It is intended to foster collaboration, inspire further research, and drive innovation in genetics and therapeutic development.</p> <p>&nbsp;</p>

opencc-by-4.0Oct 2024View details →
geo24/100

En bloc and segmental deletions of human XIST reveal X chromosome inactivation-involving RNA elements

GEO Series GSE65830. Homo sapiens. 29 samples. Type: Expression profiling by high throughput sequencing; Other.

openGEO-OpenJan 2019View details →
geo24/100

XIST dampens X chromosome activity in a SPEN-dependent manner during early human development [MeD-seq]

GEO Series GSE246640. Homo sapiens. 3 samples. Type: Methylation profiling by high throughput sequencing.

openGEO-OpenApr 2024View details →
geo24/100

Emergence of Non-Random Chromosomal Alterations (Trisomy 7 and 20) Derived from Diploid Human Colonic Epithelial Cells

GEO Series GSE24092. Homo sapiens. 2 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.

openGEO-OpenSep 2010View details →
geo24/100

Oncogenic lncRNAs alter epigenetic memory at a fragile chromosomal site in human cancer cells

GEO Series GSE180959. Homo sapiens. 13 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.

openGEO-OpenMar 2022View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

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

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