Closed jingling000 closed 4 months ago
Hi @jingling000,
Thank you for the question. I have been checking what could be the reason that caused this issue, and I recently updated the LD_pruning function, which may be relevant. Could you please install the latest version of the STAARpipeline package and try it again?
Best, Xihao
Hi Xihao, Thank you very much for your help. I have resolved my issue. Best, Jingling
When I execute the script STAARpipelineSummary_Known_Loci_Pruning.r, there are several chromosomes that did not generate corresponding data, and the error is as follows: used (Mb) gc trigger (Mb) max used (Mb) Ncells 283209 15.2 664320 35.5 450929 24.1 Vcells 487090 3.8 8388608 64.0 1815701 13.9 [1] 8
of selected samples: 3,508
of selected variants: 2
of selected samples: 3,508
of selected variants: 2
of selected samples: 3,508
of selected variants: 4,303,007
of selected samples: 3,508
of selected variants: 1
of selected samples: 3,508
of selected variants: 4,303,007
of selected samples: 3,508
of selected variants: 2
Error in lm.fit(x, y, offset = offset, singular.ok = singular.ok, ...) : 没有(非NA)案例可用 Calls: LD_pruning -> Individual_Analysis_cond -> lm -> lm.fit 停止执行 Is the reason for this that the provided known pathogenic loci do not exist in my data? If so, how can I avoid conflicts between removing certain regions during QC and this step?
Thank you for your help.