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URL: https://github.com/aroth85/pyclone
Proper Citation: Pyclone (RRID:SCR_016873)
Description: Software tool to infer the prevalence of point mutations in heterogeneous cancer samples. Probabilistic model for inferring clonal population structure from deep NGS sequencing.
Synonyms: PyClone
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: PMID:24633410
Keywords: infer, prevalence, point, mutation, heterogeneous, cancer, probabilistic, population, NGS, sequencing, data, analysis
Availability: Available for download, Free for academic, nonprofit use
Resource Name: Pyclone
Resource ID: SCR_016873
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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
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