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Broad Institute Center for Mendelian Genomics

ABSTRACT:

The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underlie Mendelian conditions. By discovering genes that cause Mendelian conditions, we will expand our understanding of their biology to facilitate diagnosis and new treatments.

PROVIDER: phs001272 | dbGaP |

SECONDARY ACCESSION(S): PRJNA368674PRJNA368673

REPOSITORIES: dbGaP

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Dataset's files

Source:

			Action	DRS
	GapExchange_phs001272.v1.p1.xml	Xml
	dbGaPEx2.1.5.xsd	Other
	Study_Report.phs001272.BroadCMG.v1.p1.MULTI.pdf	Pdf
	manifest_phs001272.BroadCMG.v1.p1.c1.GRU.pdf	Pdf
	manifest_phs001272.BroadCMG.v1.p1.c2.DS-KRD-RD.pdf	Pdf

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