Gene expression counts from induced Pluripotent Stem Cells
Authors/Creators
- 1. Technical University of Munich
- 2. European Molecular Biology Laboratory
Description
File description:
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Gene-level counts using the gtf file from the release 34 of GENCODE https://www.gencodegenes.org/human/release_34
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Split counts spanning from one exon to another using an annotation-free algorithm, therefore capturing new splice sites
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Non-split counts covering exon-intron boundaries
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Sample annotation describing each sample from the dataset
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Description file with global information from the dataset
Use: The count matrices are intended to help researchers that are interested in using RNA-Seq data with the purpose of diagnostics. Researchers can merge their own dataset with the downloaded ones, provided the tissue, genome build, strand, and paired-end specifications match. Afterwards, the workflow DROP can be used to compute expression and splicing outliers (https://github.com/gagneurlab/drop).
Maintainer: Vicente A. Yépez, yepez@in.tum.de
URL: https://github.com/gagneurlab/drop/
Title: induced Pluripotent Stem Cells
Number of samples: 330
Tissue: iPSCs
Organism: Homo sapiens
Genome assembly: hg19
Gene annotation: gencode34
Disease: None
Strand specific: True
Paired end: True
Dataset contact: Marc Bonder, marcj89 at gmail.com
Citation: Cite both the resource using Zenodo's citation and the publication under References
Files
Files
(368.3 MB)
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md5:5d179ae7b32b4f09d7385157fd5df2ac
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Additional details
References
- Bonder, M.J., Smail, C., Gloudemans, M.J. et al. Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nat Genet 53, 313–321 (2021). https://doi.org/10.1038/s41588-021-00800-7