--- license: apache-2.0 tags: - sentence-transformers - cross-encoder - reranker - modchembert - cheminformatics - smiles - generated_from_trainer - dataset_size:3193917 - loss:MultipleNegativesRankingLoss base_model: Derify/ModChemBERT-IR-BASE pipeline_tag: text-ranking library_name: sentence-transformers metrics: - map - mrr@10 - ndcg@10 co2_eq_emissions: emissions: 3666.7922463213226 energy_consumed: 17.863338649668595 source: codecarbon training_type: fine-tuning on_cloud: false cpu_model: AMD Ryzen 7 3700X 8-Core Processor ram_total_size: 62.69877243041992 hours_used: 29.477 hardware_used: 2 x NVIDIA GeForce RTX 3090 model-index: - name: 'Derify/ChemRanker-alpha-qed-sim' results: - task: type: cross-encoder-reranking name: Cross Encoder Reranking dataset: name: Unknown type: unknown metrics: - type: map value: 0.4266379953496367 name: Map - type: mrr@10 value: 0.6710111071325281 name: Mrr@10 - type: ndcg@10 value: 0.6901091880496036 name: Ndcg@10 --- # Derify/ChemRanker-alpha-qed-sim This [Cross Encoder](https://www.sbert.net/docs/cross_encoder/usage/usage.html) is finetuned from [Derify/ModChemBERT-IR-BASE](https://huggingface.co/Derify/ModChemBERT-IR-BASE) using hard-negative triplets derived from [Derify/pubchem_10m_genmol_similarity](https://huggingface.co/datasets/Derify/pubchem_10m_genmol_similarity). Positive SMILES pairs are first filtered by quality and similarity constraints, then reduced to one strongest positive target per anchor molecule to create a high-signal training set for reranking. The model computes relevance scores for pairs of SMILES strings, enabling SMILES reranking and molecular semantic search. For this variant, the positives are selected with a composite ranking criterion that combines high QED and similarity without an additional similarity-contribution cutoff. The quality stage uses strict inequality filtering (`QED > 0.85`, `similarity > 0.5`, with similarity also bounded below 1.0), and then keeps the top-scoring pair per anchor molecule. Hard negatives are mined with [Sentence Transformers](https://www.sbert.net/) using [Derify/ChemMRL-beta](https://huggingface.co/Derify/ChemMRL-beta) as the teacher model and a TopK-PercPos-style margin setting based on [NV-Retriever](https://arxiv.org/abs/2407.15831), with `relative_margin=0.05` and `max_negative_score_threshold = pos_score * percentage_margin`. Training uses triplet-format samples with 5 mined negatives per anchor-positive pair and optimizes a multiple-negatives ranking objective, while reranking evaluation uses n-tuple samples with 30 mined negatives per query. ## Model Details ### Model Description - **Model Type:** Cross Encoder - **Base model:** [Derify/ModChemBERT-IR-BASE](https://huggingface.co/Derify/ModChemBERT-IR-BASE) - **Maximum Sequence Length:** 512 tokens - **Number of Output Labels:** 1 label - **Training Dataset:** - [Derify/pubchem_10m_genmol_similarity](https://huggingface.co/datasets/Derify/pubchem_10m_genmol_similarity) Mined Hard Negatives - **License:** apache-2.0 ### Model Sources - **Documentation:** [Sentence Transformers Documentation](https://sbert.net) - **Documentation:** [Cross Encoder Documentation](https://www.sbert.net/docs/cross_encoder/usage/usage.html) - **Repository:** [Sentence Transformers on GitHub](https://github.com/huggingface/sentence-transformers) - **Hugging Face:** [Cross Encoders on Hugging Face](https://huggingface.co/models?library=sentence-transformers&other=cross-encoder) ## Usage ### Direct Usage (Sentence Transformers) First install the Transformers and Sentence Transformers libraries: ```bash pip install -U "transformers>=4.57.1,<5.0.0" pip install -U sentence-transformers ``` Then you can load this model and run inference. ```python from sentence_transformers import CrossEncoder # Download from the 🤗 Hub model = CrossEncoder("Derify/ChemRanker-alpha-qed-sim") # Get scores for pairs of texts pairs = [ ['c1snnc1C[NH2+]Cc1cc2c(s1)CCC2', 'c1snnc1CCC[NH2+]Cc1cc2c(s1)CCC2'], ['c1sc2c(c1-c1nc(C3CCOC3)no1)CCCC2', 'O=C([O-])Cc1noc(-c2csc3c2CCCC3)n1'], ['c1sc(C[NH2+]C2CC2)nc1C[NH+]1CCN2CCCC2C1', 'c1sc(C[NH2+]C2CC2)nc1C1CC([NH+]2CCN3CCCC3C2)C1'], ['c1sc(CC[NH+]2CCOCC2)nc1C[NH2+]C1CC1', 'CCc1nc(C[NH2+]C2CC2)cs1'], ['c1sc(CC2CCC[NH2+]2)nc1C1CCCO1', 'c1sc(CC2CCC[NH2+]2)nc1C1CCCC1'], ] scores = model.predict(pairs) print(scores.shape) # (5,) # Or rank different texts based on similarity to a single text ranks = model.rank( 'c1snnc1C[NH2+]Cc1cc2c(s1)CCC2', [ 'c1snnc1CCC[NH2+]Cc1cc2c(s1)CCC2', 'O=C([O-])Cc1noc(-c2csc3c2CCCC3)n1', 'c1sc(C[NH2+]C2CC2)nc1C1CC([NH+]2CCN3CCCC3C2)C1', 'CCc1nc(C[NH2+]C2CC2)cs1', 'c1sc(CC2CCC[NH2+]2)nc1C1CCCC1', ] ) # [{'corpus_id': ..., 'score': ...}, {'corpus_id': ..., 'score': ...}, ...] ``` ## Evaluation ### Metrics #### Cross Encoder Reranking * Evaluated with [CrossEncoderRerankingEvaluator](https://sbert.net/docs/package_reference/cross_encoder/evaluation.html#sentence_transformers.cross_encoder.evaluation.CrossEncoderRerankingEvaluator) with these parameters: ```json { "at_k": 10 } ``` | Metric | Value | | :---------- | :--------- | | map | 0.4266 | | mrr@10 | 0.671 | | **ndcg@10** | **0.6901** | ## Training Details ### Training Dataset #### GenMol Similarity Hard Negatives * Dataset: GenMol Similarity Hard Negatives * Size: 3,193,917 training samples * Columns: smiles_a, smiles_b, and negative * Approximate statistics based on the first 1000 samples: | | smiles_a | smiles_b | negative | | :------ | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | | type | string | string | string | | details | | | | * Samples: | smiles_a | smiles_b | negative | | :---------------------------------------------- | :------------------------------------------------- | :------------------------------------------------- | | c1sc2cc3c(cc2c1CC[NH2+]C1CC1)OCCO3 | FC(F)(F)[NH2+]CCc1csc2cc3c(cc12)OCCO3 | [NH3+]CCCc1cc2c(cc1C1CC1)OCO2 | | c1sc2cc3c(cc2c1CC[NH2+]C1CC1)OCCO3 | FC(F)(F)[NH2+]CCc1csc2cc3c(cc12)OCCO3 | COc1cc2c(cc1C[NH2+]C1CCC1)OCO2 | | c1sc2cc3c(cc2c1CC[NH2+]C1CC1)OCCO3 | FC(F)(F)[NH2+]CCc1csc2cc3c(cc12)OCCO3 | O=c1[nH]c2cc3c(cc2cc1CNC1CCCCC1)OCCO3 | * Loss: [MultipleNegativesRankingLoss](https://sbert.net/docs/package_reference/cross_encoder/losses.html#multiplenegativesrankingloss) with these parameters: ```json { "scale": 10.0, "num_negatives": 4, "activation_fn": "torch.nn.modules.activation.Sigmoid" } ``` ### Evaluation Dataset #### GenMol Similarity Hard Negatives * Dataset: GenMol Similarity Hard Negatives * Size: 165,968 evaluation samples * Columns: smiles_a, smiles_b, negative_1, negative_2, negative_3, negative_4, negative_5, negative_6, negative_7, negative_8, negative_9, negative_10, negative_11, negative_12, negative_13, negative_14, negative_15, negative_16, negative_17, negative_18, negative_19, negative_20, negative_21, negative_22, negative_23, negative_24, negative_25, negative_26, negative_27, negative_28, negative_29, and negative_30 * Approximate statistics based on the first 1000 samples: | | smiles_a | smiles_b | negative_1 | negative_2 | negative_3 | negative_4 | negative_5 | negative_6 | negative_7 | negative_8 | negative_9 | negative_10 | negative_11 | negative_12 | negative_13 | negative_14 | negative_15 | negative_16 | negative_17 | negative_18 | negative_19 | negative_20 | negative_21 | negative_22 | negative_23 | negative_24 | negative_25 | negative_26 | negative_27 | negative_28 | negative_29 | negative_30 | | :------ | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :-------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | :--------------------------------------------------------------------------------------------- | | type | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | string | | details | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | * Samples: | smiles_a | smiles_b | negative_1 | negative_2 | negative_3 | negative_4 | negative_5 | negative_6 | negative_7 | negative_8 | negative_9 | negative_10 | negative_11 | negative_12 | negative_13 | negative_14 | negative_15 | negative_16 | negative_17 | negative_18 | negative_19 | negative_20 | negative_21 | negative_22 | negative_23 | negative_24 | negative_25 | negative_26 | negative_27 | negative_28 | negative_29 | negative_30 | | :--------------------------------------------------- | :---------------------------------------------------------- | :---------------------------------------------------------- | :---------------------------------------------------- | :------------------------------------------------- | :------------------------------------------ | :-------------------------------------------------- | :----------------------------------------- | :------------------------------------------------- | :--------------------------------------------------- | :---------------------------------------------------- | :------------------------------------------------- | :------------------------------------------------------- | :----------------------------------------------- | :------------------------------------------------------ | :------------------------------------------------ | :------------------------------------------------------ | :--------------------------------------------------- | :------------------------------------------------ | :----------------------------------------------- | :---------------------------------------------------- | :----------------------------------------------- | :----------------------------------------------------- | :-------------------------------------------------- | :----------------------------------------------------- | :------------------------------------------------- | :--------------------------------------------- | :--------------------------------------------------------- | :------------------------------------------------ | :--------------------------------------------------- | :------------------------------------------------------- | :----------------------------------------------- | | c1snnc1C[NH2+]Cc1cc2c(s1)CCC2 | c1snnc1CCC[NH2+]Cc1cc2c(s1)CCC2 | c1snnc1CCC[NH2+]Cc1cc2c(s1)CCC2 | Cn1cc(C[NH2+]Cc2cc3c(s2)CCC3)nn1 | Cn1cc(CC[NH2+]Cc2cc3c(s2)CCC3)nn1 | Cc1cc(C[NH2+]Cc2csnn2)sc1C | NC(=O)c1csc(C[NH2+]Cc2cc3c(s2)CCC3)c1 | Cc1cc(CC[NH2+]Cc2csnn2)sc1C | N#CCc1csc(C[NH2+]Cc2cc3c(s2)CCC3)c1 | Ic1ccc(C[NH2+]Cc2cc3c(s2)CCC3)o1 | c1ncc(C[NH2+]Cc2csnn2)s1 | c1c(C[NH2+]CC2CC2)sc2c1CSCC2 | N#Cc1cc(F)cc(C[NH2+]Cc2cc3c(s2)CCC3)c1 | c1cc(C[NH2+]Cc2nc3c(s2)CCC3)no1 | CCc1ccc(C[NH2+]Cc2csnn2)s1 | NCc1csc(NCc2cc3c(s2)CCC3)n1 | C[NH+](Cc1cscn1)Cc1nnc(-c2cc3c(s2)CCCC3)o1 | Fc1cc(C[NH2+]Cc2cc3c(s2)CCC3)ccc1Br | FC(F)(F)C[NH2+]Cc1cc2c(s1)CCSC2 | c1cc(C[NH2+]Cc2cc3c(s2)CCC3)c[nH]1 | Cc1cc(C)c(CC[NH2+]Cc2cc3c(s2)CCC3)c(C)c1 | Oc1ccc(C[NH2+]Cc2cc3c(s2)CCC3)cc1Br | O=C([O-])c1ccc(CC[NH2+]Cc2cc3c(s2)CCC3)s1 | c1c(C[NH2+]CC2CCCC2)sc2c1CCC2 | O=C([O-])c1ccc(C[NH2+]Cc2cc3c(s2)CCC3)s1 | COc1cc(C)cc(C[NH2+]Cc2cc3c(s2)CCC3)c1 | CCc1cnc(C[NH2+]Cc2csnn2)s1 | Clc1cc(C[NH2+]Cc2cc3c(s2)CCC3)ccc1Br | c1c(C[NH2+]CC2CC2)sc2c1CCCCC2 | Cc1ccccc1C[NH2+]Cc1cc2c(s1)CCC2 | c1cc(C[NH+]2CCCC2)sc1C[NH2+]Cc1cc2c(s1)CCC2 | Cc1cc(C[NH2+]Cc2cc3c(s2)CCC3)ccc1F | | c1sc2c(c1-c1nc(C3CCOC3)no1)CCCC2 | O=C([O-])Cc1noc(-c2csc3c2CCCC3)n1 | Nc1sc2c(c1-c1nc(C3CCOC3)no1)CCCC2 | Nc1sc2c(c1-c1nc(C3CCC3)no1)CCCC2 | c1c(-c2nc(C3CCCNC3)no2)sc2c1CCCCCC2 | Nc1sccc1-c1nc(C2CCCOC2)no1 | Nc1sc2c(c1-c1nc(C3CCCO3)no1)CCCC2 | Cc1csc(-c2nc(C3CCOCC3)no2)c1N | Cc1oc2c(c1-c1nc(C3CCOC3)no1)C(=O)CCC2 | c1c(-c2nc(C3C[NH2+]CCO3)no2)sc2c1CCCCC2 | O=C([O-])Nc1sc2c(c1-c1nc(C3CC3)no1)CCCC2 | c1cc2c(s1)CCCC2c1nc(C2CC2)no1 | CC(=O)N1CCCC(c2noc(-c3cc4c(s3)CCCCCC4)n2)C1 | Cc1cc(-c2nc([C@@H]3CCOC3)no2)c(N)s1 | c1cc2c(nc1-c1noc(C3CCCOC3)n1)CCCC2 | Nc1sccc1-c1nc(C2CCCC2)no1 | c1cc2c(nc1-c1noc(C3CCOCC3)n1)CCCC2 | [NH3+]C(c1noc(-c2cc3c(s2)CCCC3)n1)C1CC1 | c1cc2c(c(-c3nc(C4CCOCC4)no3)c1)CCCN2 | c1c(-c2nc(C3CC3)no2)nn2c1CCCC2 | CN1CC(c2noc(-c3cc4c(s3)CCCC4)n2)CC1=O | O=C([O-])Cc1noc(-c2csc3c2CCCC3)n1 | Oc1c(-c2nc(C3CCC(F)(F)C3)no2)ccc2c1CCCC2 | Cc1cc(=O)c(-c2noc(C3CCCOC3)n2)c2n1CCC2 | O=C([O-])CNc1sc2c(c1-c1nc(C3CC3)no1)CCCC2 | CC1CCc2c(sc(N)c2-c2nc(C3CC3)no2)C1 | Cn1nc(-c2nc(C3CCCO3)no2)c2c1CCCC2 | O=C(Nc1sc2c(c1-c1nc(C3CC3)no1)COCC2)C1=CCCCC1 | Cc1cscc1-c1noc(C2CCOCC2)n1 | CC1(C)CCCc2sc(N)c(-c3nc(C4CC4)no3)c21 | Clc1cc2c(c(-c3nc(C4CCOC4)no3)c1)OCC2 | Nc1sc2c(c1-c1nnc(C3CC3)o1)CCCC2 | | c1sc(C[NH2+]C2CC2)nc1C[NH+]1CCN2CCCC2C1 | c1sc(C[NH2+]C2CC2)nc1C1CC([NH+]2CCN3CCCC3C2)C1 | c1sc(C[NH2+]C2CC2)nc1C1CC([NH+]2CCN3CCCC3C2)C1 | CC(C)[NH2+]Cc1nc(C[NH+]2CCC3CCCCC3C2)cs1 | CN1C2CCC1C[NH+](Cc1csc(C[NH3+])n1)CC2 | Nc1nc(CC[NH+]2CCCN3CCCC3C2)cs1 | CC1C[NH+](Cc2csc(C[NH2+]C3CC3)n2)CCN1C | Oc1csc(CN2CCCC3C[NH2+]CC32)n1 | CCc1nc(C[NH+]2CCCC3CCCCC32)cs1 | C[NH2+]Cc1csc(N2CC[NH+]3CCCC3C2)n1 | [NH3+]Cc1nc(C[NH+]2CCC3CCCCC32)cs1 | CC1CN2CCCCC2C[NH+]1Cc1csc(CC[NH3+])n1 | CCCc1nc(CN2CCCC2C2CCC[NH2+]2)cs1 | ClCCc1nc(CN2CCCC2C2CCC[NH2+]2)cs1 | c1cc(C[NH2+]C2CC2)c(C[NH+]2CCN3CCCCC3C2)o1 | O=C(Cc1nc(CCl)cs1)N1CCC[NH+]2CCCC2C1 | N#CCc1nc(C[NH+]2CCCC3CCCCC32)cs1 | CC[NH2+]Cc1csc(N2CCC3C(CCC[NH+]3C)C2)n1 | c1sc(C[NH2+]C2CC2)nc1C[NH+]1CCCCC1 | [NH3+]Cc1nc(C[NH+]2CCCC2C2CCCC2)cs1 | Cc1csc(C[NH+]2CCC3C[NH2+]CC3C2)n1 | ClOCc1csc(C[NH+]2CC3C[NH2+]CC3C2)n1 | c1cc(C[NH+]2CCCN3CCCC3C2)nc(C2CC2)n1 | Cc1ccsc1C[NH2+]CCN1CCN2CCCC2C1 | c1sc(C[NH2+]C2CCCC2)nc1C[NH+]1CCCCC1 | Brc1csc(C[NH2+]CCN2CCN3CCCCC3C2)c1 | Cc1nc(CCC[NH2+]C2CCN3CCCCC23)cs1 | CCOC(=O)c1nc(CN2CC3CCC[NH2+]C3C2)cs1 | CCCC(=O)c1nc(CN2CC3CCC[NH2+]C3C2)cs1 | CC(C)(C)c1csc(CN2CCC[NH2+]C(C3CC3)C2)n1 | COCc1nc(CN2CCC([NH3+])C2)cs1 | CCC[NH2+]Cc1nc(C[NH+]2CC3CCC2C3)cs1 | * Loss: [MultipleNegativesRankingLoss](https://sbert.net/docs/package_reference/cross_encoder/losses.html#multiplenegativesrankingloss) with these parameters: ```json { "scale": 10.0, "num_negatives": 4, "activation_fn": "torch.nn.modules.activation.Sigmoid" } ``` ### Training Hyperparameters #### Non-Default Hyperparameters - `eval_strategy`: epoch - `per_device_train_batch_size`: 256 - `per_device_eval_batch_size`: 256 - `torch_empty_cache_steps`: 1000 - `learning_rate`: 3e-05 - `weight_decay`: 1e-05 - `max_grad_norm`: None - `lr_scheduler_type`: warmup_stable_decay - `lr_scheduler_kwargs`: {'num_decay_steps': 6238, 'warmup_type': 'linear', 'decay_type': '1-sqrt'} - `warmup_steps`: 6238 - `seed`: 12 - `data_seed`: 24681357 - `bf16`: True - `bf16_full_eval`: True - `tf32`: True - `dataloader_num_workers`: 8 - `dataloader_prefetch_factor`: 2 - `load_best_model_at_end`: True - `optim`: stable_adamw - `optim_args`: decouple_lr=True,max_lr=3e-05 - `dataloader_persistent_workers`: True - `resume_from_checkpoint`: False - `gradient_checkpointing`: True - `torch_compile`: True - `torch_compile_backend`: inductor - `torch_compile_mode`: max-autotune - `eval_on_start`: True - `batch_sampler`: no_duplicates #### All Hyperparameters
Click to expand - `overwrite_output_dir`: False - `do_predict`: False - `eval_strategy`: epoch - `prediction_loss_only`: True - `per_device_train_batch_size`: 256 - `per_device_eval_batch_size`: 256 - `per_gpu_train_batch_size`: None - `per_gpu_eval_batch_size`: None - `gradient_accumulation_steps`: 1 - `eval_accumulation_steps`: None - `torch_empty_cache_steps`: 1000 - `learning_rate`: 3e-05 - `weight_decay`: 1e-05 - `adam_beta1`: 0.9 - `adam_beta2`: 0.999 - `adam_epsilon`: 1e-08 - `max_grad_norm`: None - `num_train_epochs`: 3 - `max_steps`: -1 - `lr_scheduler_type`: warmup_stable_decay - `lr_scheduler_kwargs`: {'num_decay_steps': 6238, 'warmup_type': 'linear', 'decay_type': '1-sqrt'} - `warmup_ratio`: 0.0 - `warmup_steps`: 6238 - `log_level`: passive - `log_level_replica`: warning - `log_on_each_node`: True - `logging_nan_inf_filter`: True - `save_safetensors`: True - `save_on_each_node`: False - `save_only_model`: False - `restore_callback_states_from_checkpoint`: False - `no_cuda`: False - `use_cpu`: False - `use_mps_device`: False - `seed`: 12 - `data_seed`: 24681357 - `jit_mode_eval`: False - `bf16`: True - `fp16`: False - `fp16_opt_level`: O1 - `half_precision_backend`: auto - `bf16_full_eval`: True - `fp16_full_eval`: False - `tf32`: True - `local_rank`: 0 - `ddp_backend`: None - `tpu_num_cores`: None - `tpu_metrics_debug`: False - `debug`: [] - `dataloader_drop_last`: True - `dataloader_num_workers`: 8 - `dataloader_prefetch_factor`: 2 - `past_index`: -1 - `disable_tqdm`: False - `remove_unused_columns`: True - `label_names`: None - `load_best_model_at_end`: True - `ignore_data_skip`: False - `fsdp`: [] - `fsdp_min_num_params`: 0 - `fsdp_config`: {'min_num_params': 0, 'xla': False, 'xla_fsdp_v2': False, 'xla_fsdp_grad_ckpt': False} - `fsdp_transformer_layer_cls_to_wrap`: None - `accelerator_config`: {'split_batches': False, 'dispatch_batches': None, 'even_batches': True, 'use_seedable_sampler': True, 'non_blocking': False, 'gradient_accumulation_kwargs': None} - `parallelism_config`: None - `deepspeed`: None - `label_smoothing_factor`: 0.0 - `optim`: stable_adamw - `optim_args`: decouple_lr=True,max_lr=3e-05 - `adafactor`: False - `group_by_length`: False - `length_column_name`: length - `project`: huggingface - `trackio_space_id`: trackio - `ddp_find_unused_parameters`: None - `ddp_bucket_cap_mb`: None - `ddp_broadcast_buffers`: False - `dataloader_pin_memory`: True - `dataloader_persistent_workers`: True - `skip_memory_metrics`: True - `use_legacy_prediction_loop`: False - `push_to_hub`: False - `resume_from_checkpoint`: False - `hub_model_id`: None - `hub_strategy`: every_save - `hub_private_repo`: None - `hub_always_push`: False - `hub_revision`: None - `gradient_checkpointing`: True - `gradient_checkpointing_kwargs`: None - `include_inputs_for_metrics`: False - `include_for_metrics`: [] - `eval_do_concat_batches`: True - `fp16_backend`: auto - `push_to_hub_model_id`: None - `push_to_hub_organization`: None - `mp_parameters`: - `auto_find_batch_size`: False - `full_determinism`: False - `torchdynamo`: None - `ray_scope`: last - `ddp_timeout`: 1800 - `torch_compile`: True - `torch_compile_backend`: inductor - `torch_compile_mode`: max-autotune - `include_tokens_per_second`: False - `include_num_input_tokens_seen`: no - `neftune_noise_alpha`: None - `optim_target_modules`: None - `batch_eval_metrics`: False - `eval_on_start`: True - `use_liger_kernel`: False - `liger_kernel_config`: None - `eval_use_gather_object`: False - `average_tokens_across_devices`: True - `prompts`: None - `batch_sampler`: no_duplicates - `multi_dataset_batch_sampler`: proportional - `router_mapping`: {} - `learning_rate_mapping`: {}
### Training Logs | Epoch | Step | Training Loss | Validation Loss | ndcg@10 | | :-----: | :-------: | :-----------: | :-------------: | :--------: | | 0.0002 | 1 | 1.2724 | - | - | | 0.1603 | 1000 | 0.1583 | - | - | | 0.3206 | 2000 | 0.0196 | - | - | | 0.4809 | 3000 | 0.0112 | - | - | | 0.6412 | 4000 | 0.0079 | - | - | | 0.8015 | 5000 | 0.0063 | - | - | | 0.9618 | 6000 | 0.0053 | - | - | | 1.0 | 6238 | - | 1.6835 | 0.6811 | | 1.1222 | 7000 | 0.0045 | - | - | | 1.2825 | 8000 | 0.0041 | - | - | | 1.4428 | 9000 | 0.0037 | - | - | | 1.6031 | 10000 | 0.0034 | - | - | | 1.7634 | 11000 | 0.0032 | - | - | | 1.9237 | 12000 | 0.003 | - | - | | 2.0 | 12476 | - | 1.6853 | 0.6891 | | 2.0840 | 13000 | 0.0028 | - | - | | 2.2443 | 14000 | 0.0026 | - | - | | 2.4046 | 15000 | 0.0026 | - | - | | 2.5649 | 16000 | 0.0025 | - | - | | 2.7252 | 17000 | 0.0024 | - | - | | 2.8855 | 18000 | 0.0023 | - | - | | **3.0** | **18714** | **-** | **1.6982** | **0.6901** | * The bold row denotes the saved checkpoint. ### Environmental Impact Carbon emissions were measured using [CodeCarbon](https://github.com/mlco2/codecarbon). - **Energy Consumed**: 17.863 kWh - **Carbon Emitted**: 3.667 kg of CO2 - **Hours Used**: 29.477 hours ### Training Hardware - **On Cloud**: No - **GPU Model**: 2 x NVIDIA GeForce RTX 3090 - **CPU Model**: AMD Ryzen 7 3700X 8-Core Processor - **RAM Size**: 62.70 GB ### Framework Versions - Python: 3.13.7 - Sentence Transformers: 5.1.2 - Transformers: 4.57.1 - PyTorch: 2.9.0+cu128 - Accelerate: 1.11.0 - Datasets: 4.4.1 - Tokenizers: 0.22.1 ## Citation ### BibTeX #### Sentence Transformers ```bibtex @inproceedings{reimers-2019-sentence-bert, title = "Sentence-BERT: Sentence Embeddings using Siamese BERT-Networks", author = "Reimers, Nils and Gurevych, Iryna", booktitle = "Proceedings of the 2019 Conference on Empirical Methods in Natural Language Processing", month = "11", year = "2019", publisher = "Association for Computational Linguistics", url = "https://arxiv.org/abs/1908.10084", } ``` #### NV-Retriever ```bibtex @misc{moreira2025nvretrieverimprovingtextembedding, title={NV-Retriever: Improving text embedding models with effective hard-negative mining}, author={Gabriel de Souza P. Moreira and Radek Osmulski and Mengyao Xu and Ronay Ak and Benedikt Schifferer and Even Oldridge}, year={2025}, eprint={2407.15831}, archivePrefix={arXiv}, primaryClass={cs.IR}, url={https://arxiv.org/abs/2407.15831}, } ```