novoSNP, a novel computational tool for sequence variation discovery

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Figure 1.
Figure 1.

The graphical user interface. (A) The main frame, displaying trace files centered on a T/C SNP. (B) Window displaying an overview of the files in this project. (C) Window displaying the potential variations. The three checkboxes indicate whether a variation is approved (ok, +), rejected (not ok, -), or uncertain (?). (D) Sequence file names of the clustered sequence trace files. (E) The multifunctional toolbar.

This Article

  1. Genome Res. 15: 436-442

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