simuG: a general-purpose genome simulator
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Updated
May 25, 2022 - Perl
simuG: a general-purpose genome simulator
Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data
A straightforward and complete next-generation sequencing read simulator
A scalable variant calling and benchmarking framework supporting both short and long reads.
Explore and filter structural variant calls from Lumpy and Delly VCF files
An accurate pipeline for predicting the pathogenicity of human exon structural variants
My lab book for current project: Identifying structural variation in WGS data
bionano annovar annotation
Integrated analysis of Structural and Copy Number Variants on clinical targeted sequencing data
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