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Resource Name
SDMINP
RRID:SCR_009377 RRID Copied      
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SDMINP (RRID:SCR_009377)
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Resource Information

URL: https://www.dkfz.de/en/epidemiologie-krebserkrankungen/software/software.html

Proper Citation: SDMINP (RRID:SCR_009377)

Description: THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 24,2023. Software program for fast calculation of empirical and adjusted p-values for correlated and uncorrelated hypotheses in multiple testing experiments. It is based on the Free Step-Down Resampling Method for controlling the Family Wise Error Rate, originally proposed by Westfall and Young (1993), and implements a variation of the efficient algorithm of Ge et al. (2003), in which the originally necessary re-sampling effort was reduced considerably and the method made computationally more feasible. The program is independent of the underlying test statistic and works with provided observed and permutation test statistics. (entry from Genetic Analysis Software)

Abbreviations: SDMINP

Synonyms: Step-Down MIN P-value

Resource Type: software application, software resource

Keywords: gene, genetic, genomic, python 2.3.5, unix, linux, ms-windows

Availability: THIS RESOURCE IS NO LONGER IN SERVICE

Resource Name: SDMINP

Resource ID: SCR_009377

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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