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Thank you for developing such an advanced deep-learning model that is user-friendly.
I would appreciate your feedback on the feasibility of my approach to generating a cell-type-enriched ChromBPNet model.
Specifically, I am interested in a ChromBPNet model that predicts counts and profiles in photoreceptor-enriched open chromatin regions (OCRs) to extract the unique sequence grammar of photoreceptor cells. The photoreceptor-enriched OCRs were generated by subtracting OCRs from the other OCRs of the other cell types (e.g., bipolar cells, etc.) in single-cell ATAC-seq data of retinas. The photoreceptor model will be trained only with photoreceptor-enriched OCRs. The bias model is trained with all photoreceptor OCRs, and nonpeak regions are defined with photoreceptor OCRs BEFORE the subtraction.
I would appreciate any comments and feedback on my approach.
Thanks,
Yohei Ogawa
The text was updated successfully, but these errors were encountered:
Dear ChromBPNet developers,
Thank you for developing such an advanced deep-learning model that is user-friendly.
I would appreciate your feedback on the feasibility of my approach to generating a cell-type-enriched ChromBPNet model.
Specifically, I am interested in a ChromBPNet model that predicts counts and profiles in photoreceptor-enriched open chromatin regions (OCRs) to extract the unique sequence grammar of photoreceptor cells. The photoreceptor-enriched OCRs were generated by subtracting OCRs from the other OCRs of the other cell types (e.g., bipolar cells, etc.) in single-cell ATAC-seq data of retinas. The photoreceptor model will be trained only with photoreceptor-enriched OCRs. The bias model is trained with all photoreceptor OCRs, and nonpeak regions are defined with photoreceptor OCRs BEFORE the subtraction.
I would appreciate any comments and feedback on my approach.
Thanks,
Yohei Ogawa
The text was updated successfully, but these errors were encountered: