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URL: http://patchwork.r-forge.r-project.org/
Proper Citation: Patchwork (RRID:SCR_000072)
Description: Software tool for analyzing and visualizing allele-specific copy numbers and loss-of-heterozygosity in cancer genomes. The data input is in the format of whole-genome sequencing data which enables characterization of genomic alterations ranging in size from point mutations to entire chromosomes. High quality results are obtained even if samples have low coverage, ~4x, low tumor cell content or are aneuploid. Patchwork takes BAM files as input whereas PatchworkCG takes input from CompleteGenomics files. TAPS performs the same analysis as Patchwork but for microarray data.
Abbreviations: Patchwork
Resource Type: software resource
Defining Citation: PMID:23531354
Keywords: genome, allele, copy number, bam, unix, r, bio.tools
Related Condition: Cancer, Tumor
Availability: Free, Available for download, Freely available
Resource Name: Patchwork
Resource ID: SCR_000072
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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