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Flanking Sequence (version 1.0.0)
Datasets in gd_snp format have the columns in the metadata, all others need the columns chosen.

Dataset formats

The input dataset is in tabular format and must contain a scaffold or chromosome column and a position column. The output is in fasta format or Boulder-IO format used by Primer3. (Dataset missing?)


What it does

This tool reports a DNA segment containing each SNP, with up to 200 nucleotides on either side of the SNP position, which is indicated by "n". Fewer nucleotides are reported if the SNP is near an end of the assembled genome fragment.


Example