hum0018 Release Note
| Research ID | Release Date | Type of Data |
|---|---|---|
| hum0018.v2 | 2025/07/16 | NGS (Exome, WGS, RNA-seq) |
| hum0018.v1 | 2015/02/03 | NGS (Exome) |
hum0018.v2
gDNA/RNA extracted from peripheral blood cells or brain tissues of patients with 69 Charcot-Marie-Tooth disease (CMT), 21 Frontotemporal dementia (FTD), 121 Familial amyotrophic lateral sclerosis (Familial ALS), 85 Myopathy, 490 Sporadic amyotrophic lateral sclerosis (Sporadic ALS), 9 Motor neuron disease (MND) and 465 Spastic paraplegia were used for whole exome sequencing, whole genome sequencing and RNA sequencing analyses (fastq format files).
hum0018.v1
gDNAs extracted from peripheral blood cells of 14 patients with multiple system atrophy and 7 healthy control subjects were used for Exome sequencing analysis (fastq format files). Exons were captured using the SureSelect Human All Exon 50 Mb Kit and multiplex sequence was performed with the Illumina HiSeq 2000 sequencer (100 bp, Paired-end).
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