Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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We extracted DNA from whole blood or lymphoblast-derived cell lines and assessed the DNA quality with PicoGreenTM and gel electrophoresis. Whole genome sequencing was performed (Illumina HiSeq2000 and Illumina HiSeq X). WGS reads were mapped to the human reference genome assembly hg19 (GRCh37) using Burrows-Wheeler Aligner v.0.7.12 (TCAG) or Isaac v.2.0.13 (Macrogen). For each genome, we performed local realignment and quality recalibration and detected SNVs and small indels using GATK ... (Show More)
|HiSeq X Five,Illumina HiSeq 2000||112|