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while conducting a research with a small sample size (5-6) with a large exome size (21-25), should you go for Sanger sequencing or NGS? Keeping cost, labour and practicality in context.
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I read a paper where they converted WGS to core genome to check for AMR through resfinder, any insights would be appreciated, new to bioinformatics.
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I learnt to add 1 sequence at once but couldn't find an option to upload a bunch at once, still a tyro at bioinformatics, any leads?
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