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It is available from the Tools ‣ DNA assembly submenu NGS data analysis submenu of the main menu.
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<center> <br> <img src="/wiki/download/attachments/17467779/Short read aligner.png"/> <br> </center> |
Select the Align short reads item the Map Reads to reference item to align short reads to a DNA sequence or Build index item for reads mapping item to build an index for a DNA sequence which can be used to optimize aligning short reads to the sequence.
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