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Report abuseThese scripts were developed for a project at UCLA to compare structural variants found by various tools to known structural variants. It includes a very primitive structural variant type categorizer.
Python
Guide to installing, using, and interpreting structural variant finders. Includes example scripts for running tools on UCLA's Hoffman2 and a description of how to use the machine learning combinati…
Shell
Forked from nicholasjcooper/plumbCNV
generalized version of Nicholas Cooper's plumbCNV for CNV calling from microarray data
R
Code for merging Plink genotyping files with different reference genomes and genotyping chips.
Shell
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