Does anyone have any experience with library preparation of chromosome sorted DNA? The main issue is that we are starting with only 120ng of material. The good news is that we don't have to do any hybridization/capture, so we just have to repair the ends, add the A, ligate the adaptor and PCR the library. Any guidance from people who have sequenced this type of material would be very much appreciated.
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NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...10-30-2026, 06:46 AM
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