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Is it ok to keep the sequence in reverse complement mode in the new output.fasta or not?. How to deal with this behaviour? Is there a way to order the sequence as the original.fasta file?
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discussion General Discussion
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Can we use illumina paired-end assembled reference genome for integrating long reads to improve the assembly? I heard it's only for mate-pair end assembled reference genome?
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- faraz89
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- 2017-11-05 12:15:15
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