smCounter: a versatile UMI-aware variant caller to detect both somatic and germline SNVs and indels. Published in article "Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller", BMC Genomics, 2017 18:5. https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-016-3425-4
Thanks for the great tool! I am wirking with QIAseq DNA panels and I am working using smCounter. However, all the variants that I am detecting are tagged at least as LSM. I am not quite sure what does this mean and what could be the problem of the samples. Example code:
Hi, this is not an Error Report.
I was wondering, since we have regularly nearly 100 runs with smCounter, if it would be possible in any way to serialize the runs. Our computing power allows only one run per timepoint and not parralel. So preferable it would be to automatize: if run1 is finished then start run2 ....and so on.
Hi there, in addition to some of the dependencies mentioned in the README, could you please also mention the required/tested versions for pysam, scipy and Bedtools?
Thanks, Andreas