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A versatile toolkit for molecular QTL mapping and meta-analysis at scale
Corbin Quick, Li Guan, Zilin Li, Xihao Li, Rounak Dey, Yaowu Liu, Laura Scott, Xihong Lin
bioRxiv 2020.12.18.423490; doi: https://doi.org/10.1101/2020.12.18.423490
The performance gained by increasing more common factors seems to stop at ~30 for all three dataset. And by default N cannot be zero. So the default of N is set to be 30
Noted, setting N = 30 will force the output to have 30 factors.
The text was updated successfully, but these errors were encountered:
Due to #162, a run with bicv factor was initiated to avoid factor analysis being a blocker. In this initiated analysis. The factor is set to the same number of maximum factor set forth in the peer r wrapper.
Setting 60 will provides a output with 60 factors and was finished in less than 1 hr.
Based on Figure 2A of this preprint:
The performance gained by increasing more common factors seems to stop at ~30 for all three dataset. And by default N cannot be zero. So the default of N is set to be 30
Noted, setting N = 30 will force the output to have 30 factors.
The text was updated successfully, but these errors were encountered: