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CNV detection with single-read data (bacterial genome)
I am planning to do a CNV calling for the first time and I've got Illumina single-read data (50bp). Libraries were not sequenced in paired-end because... -
pooled shRNA screen and analysis by Illumina HiSeq
Hi,
We want to do pooled shRNA screens using the TRC library. The goal is to use NGS to look at shRNA representation before and after selaction.... -
Scripture and single read?
Hello,
I'm trying to assemble Illumina data (4 sets, 160 million reads in total, good quality, about 70bp length) and am considering using...
