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URL: http://ssadedin.github.io/ximmer/
Proper Citation: Ximmer (RRID:SCR_016427)
Description: Software to help users of targeted high throughput genomic sequencing data to accurately detect copy number variants (CNVs). Framework for running and evaluating other copy number detection tools.Used for evaluating and improving performance of CNV detection in exome and targeted sequencing data.
Resource Type: data analysis software, data processing software, data visualization software, simulation software, software application, software resource
Defining Citation: DOI:10.1101/260927
Keywords: cnv, copy, number, variant, exome, targeted, sequencing, data, next, generation, genomic
Funding: Australian National Health and Medical Research Council ; National Eye Institute ; National Heart Lung and Blood Institute ; National Human Genome Research Institute ; Victorian State Government
Availability: Open source, Free, Available for download, Freely available
Resource Name: Ximmer
Resource ID: SCR_016427
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400