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URL: https://github.com/Nextomics/NextPolish
Proper Citation: NextPolish (RRID:SCR_025232)
Description: Software tool to fix base errors SNV/Indel in genome generated by noisy reads. Used to correct error bases in reference genome.
Resource Type: software application, source code, data processing software, software resource, data analysis software
Keywords: fix base errors, SNV/Indel, genome, noisy reads, correct error bases, reference genome,
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