Barely Significant
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Transcriptome driven discovery of novel candidate genes for human neurological disorders in the telomer-to-telomer genome assembly era.

Hum Genomics · 2023 · PMC10594789 · PMID 37872607

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highly significantno p-value reported
Therefore, one must assume low statistical power for the ASD/pb dataset, and consequently, I will only discuss overlapping genes with the ASD/nsc dataset and highly significant DEGs.

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