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The genetic basis of suicide attempts (SA) remains unclear. Especially the role of copy number variations (CNVs) remains to be elucidated. The present study aimed to identify susceptibility variants associated with SA among Chinese with major depressive disorder (MDD), covering both CNVs and single-nucleotide polymorphisms (SNPs).
Pubmed ID: 32554045
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Software that estimates copy number and annotates regions with copy number variants(CNV).
View all literature mentionsVisualize and analyze data generated by all of Illumina''s platforms.
View all literature mentionsA software for analyzing real-time PCR data and quantifying DNA targets. It can perform copy number analysis, report confidence in copy number, display data in table and graphic format, change analysis parameters, and view data analysis information for multiple experiments at once.
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