svr_project_by_sr

Get corresponding genes.

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Example:

    svr_all_features 3702.1 peg | svr_project_by_sr

would produce a 2-column table. The first column would contain PEG IDs for genes occurring in genome 3702.1, and the second would contain a peg believed to correspond in a second genome

The svr_corresponding_genes command can be used to map from one known genome to another. However, this command is the start of a tool for mapping specific genes to sets of corresponding genes (envision using FIGfams, subsystems, or whatever). For now we use just the technology of Solid Rectangles.

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The standard input should be a tab-separated table (i.e., each line is a tab-separated set of fields). Normally, the last field in each line would contain the PEG for which functions are being requested. If some other column contains the PEGs, use

    -c N

where N is the column (from 1) that contains the PEG in each case.

This is a pipe command. The input is taken from the standard input, and the output is to the standard output.

Command-Line Options

-c Column

This is used only if the column containing PEGs is not the last.

Output Format

The standard output is a tab-delimited file. It consists of the input file with an extra column added (a peg that is putatively an isofunctional homolog).