A tool for interpretation of copy number variation (CNV) in the context of topologically associated domains (TADs).
Genotype and phenotype; Transcription factors and regulatory sites; Genetic variation
Spector JD, Wiita AP "ClinTAD: a tool for copy number variant interpretation in the context of topologically associated domains." J Hum Genet. 2019 May;64(5):437-443. https://doi.org/10.1038/s10038-019-0573-9
PMID: 30765865
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