The applications listed here are available for use in the Discovery Environment and are documented in: Discovery Environment Manual.

Discovery Environment Applications List

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mutant interval identification

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From the mutant identification 1 pipeline (Workflow:Mutant Identification 1). A tool to take a SNP list input from a bulk segregant dataset (locations of mutant parent homozygous unique SNPs only) and determine the mutant phenotype inducing SNP interval based on allele frequency analysis (output as text file and pdf)-prioritizing blocks of conserved homozygosity with the parental dataset.

Quick Start

Test Data


Test data for this app appears at: 

Input File(s)

Use the file above as test input.

Parameters Used in App

When the app is run in the Discovery Environment, use the following parameters with the above input file(s) to get the output provided in the next section below.

  • Default parameters only, no further configuration needed.

Output File(s)

Expect 2 files as output. For a test case, the output pdf file is: and the output text file is:

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