NABEC Long-Read Whole-Genome Sequencing
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.
Consent Codes
GRUDiseases
Not applicable. All phenotype data is present in dbGaPStudy Design
Resource generation for the science communityData Types
Whole GenomeSubjects
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