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Paper Details

A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5.
Blood Cancer J
34
2018
/IGH translocations, 14q, 16q, 17p, 1p, 1q, 465 genes, 6q, 8p, BRAF, CNVs, DIS3, FAM46C, IGH, IGLL5, KRAS, MM, MYC, Multiple myeloma, NRAS, RAS, RAS mutations, SNVs, TP53, chromosomal translocations, copy number variants, myeloma, single-nucleotide variants, tumor
Author NameAffiliation
Brian S WhiteWashington University School of Medicine
Brian S White
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Catrina FronickMcDonnell Genome Institute, Washington University School of Medicine
Gregory J AhmannMayo Clinic
Elaine R MardisMcDonnell Genome Institute, Washington University School of Medicine
Elaine R MardisGenomics Institute, Nationwide Children's Hospital
Elaine R MardisMcDonnell Genome Institute, Washington University School of Medicine
Elaine R MardisGenomics Institute, Nationwide Children's Hospital
Ravi VijWashington University School of Medicine
John F DiPersioWashington University School of Medicine
Joan LevyMultiple Myeloma Research Foundation
Joan LevyChordoma Foundation
Daniel AuclairMultiple Myeloma Research Foundation
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