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Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation. Nat Methods. 2023 ;20(10):1483-1492.
. . Profiling complex repeat expansions in RFC1 in Parkinson's disease. NPJ Parkinsons Dis. 2024 ;10(1):108.
. Genome-Wide Analysis of Structural Variants in Parkinson Disease. Ann Neurol. 2023 ;93(5):1012-1022.
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