url: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/collection.cgi?study_id=phs003184.v1.p1 assay: whole genome sequencing title: ALS Compute dbGAP source: dbGaP creator: ALS Compute disease: ALS FTD species: Homo sapiens subject: Amyotrophic Lateral Sclerosis Frontotemporal Dementia dataType: raw_sequencing transcriptomics genomicVariants keywords: ALS FTD WGS whole genome sequencing platform: Illumina HiSeq X publisher: ALS Compute collection: ALS Compute contributor: ALS Compute description: The ALS Compute project centralizes the storage of Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) whole genome sequencing (WGS) data from major sequencing efforts. biospecimenType: blood individualCount: 12638