<p>NABEC: North American Brain Expression Consortium cohort utilizes a series of control brain samples that have been studied for over a decade. Several genomic assays have already been performed on this cohort including: RNA sequencing, array genotyping, short-read sequencing, CAGE sequencing, and more. Here we add an additional genomic assay to this resource by performing Oxford Nanopore Long-Read Whole-Genome Sequencing. Oxford Nanopore Long-Read sequencing allows the detection of structural variants and genome-wide methylation values. This cohort is processed with the aim of having >30X coverage, and an N50 read distribution of 25kb. FAST5 (raw data) and fastq (processed data) will be made available to qualified researchers.</p>

Study	dbGap Id	Consent Code	Disease (indication)	Data Type	Study Design	Workspaces	Participants
Unspecified	phs003224	Unrestricted access	No phenotype data present.	Whole Genome	Resource generation and using data for benchmarking of pipelines	ANVIL_NIA_CARD_Coriell_Cell_Lines_Open	3
NABEC Long-Read Whole-Genome Sequencing	phs003181	GRU	Not applicable. All phenotype data is present in dbGaP	Whole Genome	Resource generation for the science community	ANVIL_NIA_CARD_LR_WGS_NABEC_GRU	14

CARD