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Accession: PRJNA287678 ID: 287678

Homo sapiens (human)

Homo sapiens SCA10 expansion-raw sequence reads

See Genome Information for Homo sapiens
Rationale: Spinocerebellar ataxia type 10 (SCA10) is caused by the expansion of a non-coding repetitive segment of DNA. More...
AccessionPRJNA287678
Data TypeRaw sequence reads
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsMcFarland KN et al., "SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure.", PLoS One, 2015;10(8):e0135906
Grants
  • "RNA-Gain-of-Function Pathogenesis in SCA10" (Grant ID R01 NS083564, NIH National Institute of Neurological Disorders and Stroke)
SubmissionRegistration date: 22-Jun-2015
University of Florida
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments4
Publications
PubMed1
PMC1
Other datasets
BioSample4
SRA Data Details
ParameterValue
Data volume, Gbases1
Data volume, Mbytes4609

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