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Accession: PRJNA283241 ID: 283241

Homo sapiens (human)

Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2

See Genome Information for Homo sapiens
Mycosis Fungoides (MF) and Sezary Syndrome (Sz) comprise the majority of Cutaneous T-Cell Lymphoma (CTCL) cases and are characterized by clinical heterogeneity. This array of symptoms includes skin patches, plaques and tumors as well as blood involvement and erythroderma. Because the genetic basis of CTCL is still poorly understood, we performed whole-exome sequencing on 11 MF/Sz samples and their matched, normal control DNA. Upon analyzing this data, we distilled a list of an additional 494 genes to be sequenced at depth. The majority of these 494 genes were sequenced in the exons alone, however, for a small subset of these genes we sequenced the entire genomic locus in search of structural variation events. This 494 gene targeted resequencing effort was performed upon 72 patients with MF/Sz and their matched, normal control DNA. More...
AccessionPRJNA283241; dbGaP: phs000913
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 7-May-2015
NCI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments170
Other datasets
BioSample170
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases777
Data volume, Tbytes0.52
Homo sapiens encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA283242Homo sapiensGenomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2 (Stanford University)

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    Homo sapiens
    Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
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