Hi team,
First of all, thank you for your contribution — your approach to the molecule generation problem is both interesting and innovative.
I’ve been reviewing the public code and pre-trained weights. After running the sampling process to generate 100 samples and evaluating them using the Vina-family metrics, I noticed that my results differ significantly from those reported in the paper.
Could you please help me verify this or let me know if I might have made a mistake in my process?
Thanks!
- This is my config for sampling:
model:
checkpoint: ./pretrained_models/pretrained-IRDiff.pt
sample:
seed: 2021
num_samples: 100
num_steps: 1000
pos_only: False
center_pos_mode: protein
sample_num_atoms: prior
python inference.py \
--config ./configs/sampling.yml \
--train_config ./configs/training.yml \
--device 'cuda:0' \
--batch_size 25 \
--result_path ./experiments/sampled_results \
--test_prompt_indices_path ./src/test_prompt_ligand_indices_top3.pt \
--start_index 0 \
--end_index 99
python eval_split.py \
--sample_path ./experiments/sampled_results \
--verbose False \
--eval_step -1 \
--eval_start_index 0 \
--eval_end_index 26 \
--save True \
--protein_root ./data/crossdocked_v1.1_rmsd1.0 \
--atom_enc_mode add_aromatic \
--docking_mode vina_dock \
--exhaustiveness 16
#option: vina_dock|qvina
python cal_metrics_from_pt.py \
--eval_path ./experiments/sampled_results
Hi team,
First of all, thank you for your contribution — your approach to the molecule generation problem is both interesting and innovative.
I’ve been reviewing the public code and pre-trained weights. After running the sampling process to generate 100 samples and evaluating them using the Vina-family metrics, I noticed that my results differ significantly from those reported in the paper.
Could you please help me verify this or let me know if I might have made a mistake in my process?
Thanks!