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Fig. 4 | BMC Genomics

Fig. 4

From: Intellectual disability genomics: current state, pitfalls and future challenges

Fig. 4

Variant filtering flowchart. SNP – single nucleotide polymorphism; DGV – database of genomic variants; SNVs – single nucleotide variants; CNVs – copy number variants; SVs – structural variants; CSAS – canonical splicing acceptor site; CSDS – canonical splicing donor site; SAS – splicing acceptor site; SDS – Splicing donor site; Q-PCR – quantitative PCR

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