Web-based version

An Accurate and Ultra-deep Coverage Method for Large-scale SSR Genotyping with SNPs in the SSR and Flanking Region Compatible

Web-based version

An Accurate and Ultra-deep Coverage Method for Large-scale SSR Genotyping with SNPs in the SSR and Flanking Region Compatible

AMGT-TS User manual (web-based version)

Create a new project

Step 1:

Launch this function by select the menu item “New Project” on the left, then fill the following information:

  • Project name

  • Project description

  • Upload the targeted sequencing file of each sample

    we can upload more than one samples data files and there is no limit.

  • Reference files Use the default if you are not familiar with the details.

  • Remark

Then use the Next button to continue.

step1

Step 2:

  • After creating the project, we use the Start button to launch the AMGT-TS tool.

  • Then, we use the Next button to go to the result tab page.

step2

Step 3:

  • This page show the analysis result of AMGT-TS tool.

We can select the View Analysis Results of a sample, to view all the loci result information of this sample.

step3

sites

  • We can show the reads alignment graph by select a locus. In the graph, the first read is the reference read of the locus,others is from the targeted sequencing data.

alignment

Project List

projectList

We can view all the projects information by select the second menu item on the left. By select the View button to check the details of each project. There are information of each project as following:

  • Basic information Such as project name, description, the result path, etc.

  • Samples list: Same as the step 3 of “Create a new project”.

viewProject

See also