Recurrent copy number variations in human induced pluripotent stem cells

Nature Biotechnology

Volumn 29, Issue 6, 2011, Pages 488-491

  Martins Taylor, Kristen ^a   Nisler, Benjamin S ^b   Taapken, Seth M ^b   Compton, Tiwanna ^a   Crandall, Leann ^a   Montgomery, Karen Dyer ^b   Lalande, Marc ^a   Xu, Ren He ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^b WiCell Research Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H; DNA METHYLTRANSFERASE 3B; DNA TOPOISOMERASE;

CELL CULTURE; CELL LINE; CHROMOSOME 12; CHROMOSOME 17; CHROMOSOME 17P; CHROMOSOME 20Q; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME DUPLICATION; CHROMOSOME G BAND; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; EMBRYONIC STEM CELL; FIBROBLAST; GENE EXPRESSION; HUMAN; HUMAN CELL; KARYOTYPING; LETTER; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; TRISOMY 12;

CELL LINE; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 12; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; EMBRYONIC STEM CELLS; GENOME, HUMAN; HUMANS; INDUCED PLURIPOTENT STEM CELLS; KARYOTYPING;

EID: 79958109873     PISSN: 10870156     EISSN: 15461696     Source Type: Journal    
DOI: 10.1038/nbt.1890     Document Type: Letter

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