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FleurGaBru authored May 1, 2020
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- paired-end Illumina-sequencing
- adjust output (number of reads) according to your genome size and expected number of fragments (e.g. based on an *in silico* digest)
- Readfiles:
- un-demultiplexing but standard Illumina adapter trimmed (usually already done by sequencing agency)
- un-demultiplexed but standard Illumina adapter trimmed (usually already done by sequencing agency)
- No reference genome required


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