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Loading dataset is the first start of pygenomeviz of API. |
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The procedure for visualizing multiple Genbank files and MUMmer comparison link results is described as jupyter notebooks in the following document. The source code of pgv-mummer and pgv-mmseqs CLI may also help you understand the dataset preparation procedure. |
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The drawing with whole genome is possible. Can I draw some link lines with selected ranges with genome sequence, not the whole range? |
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Thank you very much! I will try it. And, I think it would be so good to draw the figure in page 2 of the attached pygenomeviz error question.odt file? |
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The procedure for visualizing multiple Genbank files and MUMmer comparison link results is described as jupyter notebooks in the following document.
https://moshi4.github.io/pyGenomeViz/getting_started/#2-4-genome-alignment-visualization-workflow
The source code of pgv-mummer and pgv-mmseqs CLI may also help you understand the dataset preparation procedure.