Is it possible, implementable, using current Galaxy tools to compare one new input VCF file (from a Tuberculosis genome) against a 1000 of preloaded and then to generate a similarity report? What tools/modules and functions to include in such pipeline? Is there any kind of software for this task?
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Question: Is it possible, implementable, using current Galaxy tools to compare one new input VCF file against a 1000 of preloaded and generate a similarity report?
21 months ago by
msprindzhuk • 50
msprindzhuk • 50 wrote:
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