AnVIL Dataset Catalog

NABEC Long-Read Whole-Genome Sequencing

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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.

ConsortiumCARD

Consent Codes

GRU

Diseases

Not applicable. All phenotype data is present in dbGaP

Study Design

Resource generation for the science community

Data Types

Whole Genome

Subjects

14