User: rosariobrancaccio

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FastQ sanger sequences -ends quality trimming
... Dear all , I'm very naive regarding bioinformatic tools. I need to trim my sanger sequences to remove bad quality 5' and 3' ends and then I will join thiese sequences in order to create a long contig ( each PCR is a piece of a viral genome and I need to recostrunct the whole genome starting from the ...
sanger sequences trim galaxy quality written 11 days ago by rosariobrancaccio0 • updated 11 days ago by Jennifer Hillman Jackson24k

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