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NCI Waldenstrom Macroglobulinemia Genome-wide Association Study

ABSTRACT:

A discovery GWAS is performed, consisting of genotyping 221 Waldenstrom macroglobulinemia (WM) cases on the Illumina Omni Express 12v1.1 platform and analyzing the genotypes together with those of 3798 previously genotyped controls in a model taking into account gender, age, and principal components of ancestry (i.e., significant eigenvectors). Directly genotyped data are supplemented by imputation using the Haplotype Reference Consortium.

PROVIDER: phs001284 | dbGaP |

SECONDARY ACCESSION(S): PRJNA371287PRJNA371288

REPOSITORIES: dbGaP

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	GapExchange_phs001284.v1.p1.xml	Xml
	dbGaPEx2.1.5.xsd	Other
	Study_Report.phs001284.FamilialBloodLymphNodeCancers_WM.v1.p1.MULTI.pdf	Pdf
	manifest_phs001284.FamilialBloodLymphNodeCancers_WM.v1.p1.c1.DS-CA-MDS.pdf	Pdf
	manifest_phs001284.FamilialBloodLymphNodeCancers_WM.v1.p1.c2.GRU.pdf	Pdf

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