Hello, I've got only about 10X depth of coverage calculating from number of reads. But I'm not sure about what is the coverage across the genome.
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Hello,
I have no shotgun data for the genome which has already been polished with PacBio, but it could do with further improvement of gene completeness. I also have Omni-C reads of 150 bp paired end, but is it conceptually ok to use this data for genome polishing? If it is, do read 1 and 2 have to be mapped separately? What are the recommendations?
Thanks.
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What are Omni-C reads ? Do you have a link ?
Omni-C is the library technology, sequencing is on Illumina platform. Here is the link: https://dovetailgenomics.com/omni-c/