Hi all, I am a complete novice at CLC genomics, and bioinformatics in general, and, with an absent PI, I am looking to the seqanswers community for help. Is anyone out there proficient enough with CLC genomics workbench to help me? I have done a batch style basic variant detection (0% threshold) of 17 E. coli genomes, all against a single reference genome, so now I have a single track with all the variants detected across all genomes. Next I want to annotate this track against a reference genome to identify more highly variable regions. I have already contacted CLC support, but am hoping to get a faster response on here. I hope this question makes sense.
-
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...10-14-2026, 09:55 AM