Publication: Copy Number Variation Analysis from SNP Genotyping Microarrays in Large Cohorts of Neurological Disorders
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Abstract
Copy number variants (CNVs) are a major source of genetic variation in the human genome, and they are highly heterogeneous in type, size, and frequency. CNVs represent the largest portion of genomic v...
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Copy number variation analysis from SNP genotyping microarrays in large cohorts of neurological disorders. Eduardo Pérez-Palma, Lisa-Marie Niestroj, Miguel Inca-Martínez, Camilo Villaman, Elif Irem Sarihan, Dennis Lal, Ignacio Mata. Book Chapter. Neuromethods. Springer Nature. DOI: 10.1007/978-1-0716-2357-2_10
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