Open AccessDetecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample
Author(s) -
P F Sullivan
Publication year - 2020
Publication title -
unc libraries
Language(s) - English
DOI - 10.17615/anx9-yy22
Subject(s) - genotyping , copy number variation , sample (material) , genetics , exome sequencing , schizophrenia (object oriented programming) , exome , biology , computational biology , genotype , medicine , mutation , gene , psychiatry , genome , chromatography , chemistry
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