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All | Alignment | Assemblers | ChIP | Copy Number Variants | Exome | Mate Pair | Methylation | Microbiome | Pathway Analysis | Proteins | SAS Macros | R Packages | RNA | SNP/SNV | Structural Variants | Survival Analysis | Visualization |
All | Alignment | Assemblers | ChIP | Copy Number Variants | Exome | Mate Pair | Methylation | Microbiome | Pathway Analysis | Proteins | SAS Macros | R Packages | RNA | SNP/SNV | Structural Variants | Survival Analysis | Visualization |
CNVNator
Structural Variations (SVs) and Copy Number Variations (CNVs) are the major source of genomic variations. CNVnator is a tool for Copy Number Variation (CNV) discovery and genotyping from depth-of-coverage by mapped reads. It accepts .bam files as input and generates CNVs calls in less than 10 hours of calculations. The source code and extended descriptions […]