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Accession: PRJNA154859 ID: 154859

Homo sapiens (human)

SNP data from 30 pheochromocytomas and paragangliomas.

See Genome Information for Homo sapiens
SNP profiles from 30 pheochromocytomas and paragangliomas were analyzed to detect identical-by-descent haplotypes, highlighting a founder mutation of SDHD in two samples. More...
AccessionPRJNA154859; GEO: GSE32204
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsLetouzé E et al., "Identity by descent mapping of founder mutations in cancer using high-resolution tumor SNP data.", PLoS One, 2012;7(5):e35897
SubmissionRegistration date: 23-Mar-2012
Programme "Cartes d'Identité des Tumeurs", Ligue Contre Le Cancer
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots18627030
Data volume, Processed Mbytes991

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