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GSE107896

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Widespread RNA editing dysregulation in Autism Spectrum Disorders

Organism: Homo sapiens
Platform: GPL20301
Samples: 12
Experiment Types:
Expression profiling by high throughput sequencing
Submitted: Dec 11 2017
Last Updated: May 15 2019
Status: Public on Dec 14 2018
Contact: Grace,,Xiao (UCLA)

Relations

SuperSeries of: GSE107867 SuperSeries of: GSE107895 BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA421887

Summary

This SuperSeries is composed of the SubSeries listed below.

Overall Design

Refer to individual Series

Analysis (14 steps)

View Data Processing
Processing steps for GSE107896
  1. Map fastq reads with HISAT2 hisat2 -q --phred64 -x grch37_tran/genome_tran --no-unal --reorder --no-mixed
  2. Extract uniquely mapped reads from SAM files
  3. Remap unmapped reads with hyperediting pipeline.
  4. In brief, convert all adenosines to guanosines and align to modified hg19 genome where adenosines are also substituted by guanosines.
  5. Obtain uniquely mapped reads pairs from hyperediting pipeline and combine with uniquely mapped reads from first round of read mapping
  6. Identify RNA-DNA differences between mapped reads and hg19 reference genome.
  7. Apply log-likelihood test to determine whether RDD is likely resulted from sequencing error (Bahn et. al.
  8. PMID: 21960545)
Showing first 8 steps.

Supplementary Files (1)

GSE107896_RAW.tar Download
GEO Samples (12)

Dataset Citations (1)

Widespread RNA editing dysregulation in brains from autistic individuals.
PMID 30559470 · 2019 · Nature neuroscience
Stephen S Tran, Hyun-Ik Jun, Jae Hoon Bahn, Adel Azghadi, Gokul Ramaswami, Eric L Van Nostrand, Thai B Nguyen, Yun-Hua E Hsiao, Changhoon Lee, Gabriel A Pratt, Verónica Martínez-Cerdeño, Randi J Hagerman, Gene W Yeo, Daniel H Geschwind, Xinshu Xiao

Linked Publications (1)