File description: Gene-level counts using the gtf file from the release 29 of GENCODE https://www.gencodegenes.org/human/release_29 Split counts spanning from one exon to another using an annotation-free algorithm, therefore capturing new splice sites Non-split counts covering exon-intron boundaries Sample annotation describing each sample from the dataset 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 DROP pipeline can be used to compute expression and splicing outliers (https://github.com/gagneurlab/drop). Maintainer: Vicente A. Yépez, yepez@in.tum.de Title: Gene expression and splicing counts from amniotic fluid cells Number of samples: 56 Tissue: Amniotic fluid cells Organism: Homo sapiens Genome assembly: hg19 Gene annotation: gencode29 Disease ICD-10: Q89: F2100984A and F2100985, Q23: F1901567 and Q74: F2000845 Strand specific: False Paired end: True Cite as: Cite both the resource using Zenodo's citation and the publication under References Dataset contact: Brian Chung bhychung@hku.hk Comments: A total of 56 RNA-seq samples were used for running pipeline. Out of those, 52 samples were included in the manuscript.