ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE106773
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ArrayCGH was performed on a cohort of 25 specimens collected from children with newly diagnosed T-ALL characterized by TCRAD-MYC translocation ArrayCGH analyses were perfomed to study genomic aberrations occurring in the rare subgroup of TCRAD-MYC rearranged T-ALL 25 DNA samples from pediatric T-ALL patients at diagnosis were analyzed on the Agilent SurePrint G3 Human CGH microarrays (G4449A, design ID: 022060). For every sample, the gender-matched control was labeled in parallel and hybridized together
创建时间:
2018-07-03



