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UK10K_NEURO_ASD_FI REL-2012-11-27
UK10K_NEURO_ASD_FI REL-2012-11-27
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ega-archive.org相关数据集
Single-cell transcriptome sequencing
Raw reads from single-cell RNA-sequencing of peripheral blood of five TET2 mutation carriers as well as three non-carrier family members. Single-cells were captured into 10x barcoded gel beads and RNA
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Summary statistics across all datasets.
The sum of each of the test statistics across all of the SNPs in each of the diseases. LTPub vs LogR is the % increase of LTPub compared to LogR. It has a median value of 16%. Type 2 diabetes (T2D), p
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Supporting data for “Molecular Basis of Human Complex Diseases”.
This dataset contains all of the source code used in the analysis described in the paper "Molecular Basis of Human Complex Diseases." The dataset contains codes for the three main results mentioned in
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Additional file 10 of Genomic analysis of circular RNAs in heart
Additional file 10. Table S5. List of high-confidence and significantly dysregulated circRNAs in DCM compared to normal heart samples. Chromosome coordinates are in hg38 annotation. The threshold for
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4C-seq: Three-dimensional chromatin interactions of FMR1, HTT, DMPK, and GFP viewpoints.
Expanded CAG/CTG repeats underlie thirteen neurological disorders, including myotonic dystrophy type 1 (DM1) and Huntington's disease (HD). Upon expansion, CAG/CTG repeat loci acquire heterochromatic
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