Sentence-BERT: Sentence Embeddings using Siamese BERT-Networks
Paper • 1908.10084 • Published • 16
How to use jagadeesh/zeiss-re-1757443344 with sentence-transformers:
from sentence_transformers import SentenceTransformer
model = SentenceTransformer("jagadeesh/zeiss-re-1757443344")
sentences = [
"Achieving high cell transfection efficiency is essential for various cell types in numerous disease applications. However, the efficient introduction of genes into natural killer (NK) cells remains a challenge. In this study, we proposed a design strategy for delivering exogenous genes into the NK cell line, NK-92, using a modified non-viral gene transfection method. Calcium phosphate/DNA nanoparticles (pDNA-CaP NPs) were prepared using co-precipitation methods and combined with low-voltage pulse electroporation to facilitate NK-92 transfection. The results demonstrated that the developed pDNA-CaP NPs exhibited a uniform diameter of approximately 393.9 nm, a DNA entrapment efficiency of 65.8%, and a loading capacity of 15.9%. Furthermore, at three days post-transfection, both the transfection efficiency and cell viability of NK-92 were significantly improved compared to standalone plasmid DNA (pDNA) electroporation or solely relying on the endocytosis pathway of pDNA-CaP NPs. This study provides valuable insights into a novel approach that combines calcium phosphate nanoparticles with low-voltage electroporation for gene delivery into NK-92 cells, offering potential advancements in cell therapy.",
"ZEISS Airyscan is an advanced imaging technology that enhances traditional confocal microscopy by using a 32-channel detector to capture more light with higher resolution and sensitivity. Unlike standard confocal systems that rely on a single pinhole, Airyscan collects the entire Airy disk pattern and reconstructs images for super-resolution clarityâ down to 120 nm laterally. This results in significantly improved signal-to-noise ratio and reduced photodamage, making it ideal for detailed imaging of live cells and biological samples. It's compatible with ZEISS LSM systems like the LSM 880 and 900, offering researchers a powerful tool for high-precision fluorescence microscopy",
"the zeiss lsm 900 with airyscan 2 is a compact confocal microscope designed for high-quality imaging and intelligent analysis of biological samples, supporting a wide range of research applications from resolving nanoscale structures to observing dynamic processes in living systems. its key technologies enable researchers to acquire detailed and quantitative data while maintaining sample integrity and maximizing experimental efficiency. key research and application areas: - super-resolution imaging: investigating the ultrastructure of biological specimens by achieving resolution beyond the diffraction limit (down to 90 nm laterally) through airyscan 2 and joint deconvolution (jdcv). this allows for the detailed visualization of cellular and molecular architecture. - gentle live cell imaging: studying biological processes in living organisms with minimized phototoxicity and photobleaching due to optimized components and sensitive detectors. this facilitates long-term observation of cellular dynamics and molecular interactions without disturbing the sample. - fast multiplex imaging: acquiring data from multiple fluorescent labels or large fields of view rapidly using multiplex modes of airyscan 2, enabling the study of dynamic events and efficient screening of samples. - enhanced confocal imaging: improving the signal-to-noise ratio and resolution of standard confocal imaging through lsm plus, allowing for better data quality in multi-color and live cell experiments with minimal user interaction. - molecular dynamics analysis: determining molecular concentration, diffusion, and flow in living samples using the zeiss dynamics profiler, which leverages the unique capabilities of the airyscan 2 detector for advanced spatial cross-correlation analyses. this enables the study of molecular behavior in various biological contexts, including flow in microfluidic systems and blood vessels and asymmetric diffusion in cellular condensates. - automated and reproducible experiments: streamlining complex imaging workflows with zen microscopy software, including features like ai sample finder for rapid region of interest identification and smart setup for automated application of optimal imaging settings. the experiment designer module allows for the creation of sophisticated, repeatable imaging routines. - correlative microscopy: integrating data from different imaging modalities and sources using zen connect to provide a comprehensive understanding of the sample, from overview to high-resolution details, including the possibility of correlative cryo microscopy workflows. typical sample types: - cultured cells and cell lines: for studying subcellular structures, dynamics, and responses to stimuli. - tissues and tissue sections: to investigate cellular organization, protein localization, and interactions within a complex environment. - small model organisms and embryos: such as drosophila and zebrafish for in vivo studies of development, physiology, and disease. - organoids and 3d cell cultures: for studying tissue architecture and development in vitro. - plant samples: such as pollen grains, for investigating cellular structures. - samples requiring correlative microscopy: like yeast cells for cryo-em workflows. - microfluidic systems: for controlled studies of fluid dynamics and molecular flow. commonly performed tasks: - confocal laser scanning microscopy: obtaining high-resolution optical sections of samples to visualize internal structures and create 3d reconstructions. - super-resolution imaging with airyscan: resolving nanoscale details beyond the limits of conventional light microscopy. - live cell imaging: capturing time-lapse sequences of living samples to study dynamic biological processes. - multi-color fluorescence imaging: simultaneously detecting multiple fluorescent probes to study the co-localization and interactions of different molecules. - spectral imaging and unmixing: separating the signals of spectrally overlapping fluorophores for accurate multi-target analysis. - quantitative image analysis: extracting meaningful data from images, including measurements of intensity, area, distance, and co-localization, using tools within zen software and the bio apps toolkit. - automated sample identification and imaging: utilizing ai sample finder to quickly locate and image regions of interest on various sample carriers. - analysis of molecular dynamics: measuring parameters such as diffusion coefficients, flow speeds, and molecular concentrations using the dynamics profiler. - creating 3d and 4d visualizations: reconstructing volumetric datasets and generating animations to understand spatial and temporal relationships within samples. - correlating light and electron microscopy data: combining functional light microscopy data with ultrastructural details from electron microscopy. - performing bleaching experiments: such as frap, to study molecular mobility within cellular compartments (although frap is mentioned in the software features , no specific application examples are provided in the excerpts). - tiling and multi-position imaging: acquiring large datasets by automatically imaging and stitching together multiple adjacent fields of view or imaging multiple regions of interest.",
"the zeiss sigma family of field emission scanning electron microscopes (fe-sems) offers versatile solutions for high-quality imaging and advanced analytical microscopy across a multitude of scientific and industrial domains. these instruments are engineered for reliable, high-end nano-analysis, combining fe-sem technology with an intuitive user experience to enhance productivity. key research and application areas: - advancing materials science: facilitating the development and understanding of novel materials by enabling the investigation of micro- and nanoscale structures. this includes characterizing metals, alloys, polymers, catalysts, and coatings for various applications such as electronics and energy. - driving innovation in nanoscience and nanomaterials: providing capabilities for the analysis of nanoparticles, thin films, 2d materials (like graphene and mos2), and other nanostructures to understand their properties and potential applications. - supporting energy research: enabling the study of materials and devices relevant to energy storage and conversion, such as battery components, to improve their performance and longevity. - enabling life sciences investigations: allowing for the exploration of the ultrastructural details of biological samples, including cells, tissues, spores, and diatoms, often utilizing low voltage to minimize beam damage. - contributing to geosciences and natural resources: supporting the characterization of rocks, ores, and minerals for improved understanding, processing, and modeling in geology and related fields. - ensuring quality in industrial applications: serving as a vital tool for failure analysis of mechanical, optical, and electronic components, as well as for quality inspection of particles and materials to meet defined standards. typical sample types: - a wide variety of materials including metals, ceramics, polymers, composites, thin films, and coatings. - nanomaterials such as nanoparticles, nanotubes, nanowires, and 2d crystals. - biological specimens encompassing cells, tissues, bacteria, fungi (e.g., spores), and diatoms. - geological samples including rocks, minerals, ores, and thin sections. - particulates for quality inspection and technical cleanliness analysis. - non-conductive samples such as polymers, biological tissues, and ceramics, often analyzed without coating using variable pressure modes. - beam-sensitive samples like biological materials and some nanomaterials, which can be imaged at low voltages to prevent damage. commonly performed tasks: - high-resolution imaging of sample surfaces and internal structures, often at low accelerating voltages (e.g., 1 kv and below) to enhance resolution and contrast, especially on challenging samples. - material contrast imaging to visualize different phases or compositions within a sample using backscattered electron (bse) detectors. - elemental analysis and mapping using energy dispersive x-ray spectroscopy (eds) to determine the chemical composition and distribution of elements in a sample. - variable pressure (vp) imaging and analysis of non-conductive and outgassing samples without the need for conductive coatings, often utilizing nanovp lite mode to minimize the skirt effect and enhance image quality and analytical precision. - crystallographic orientation imaging using techniques like electron backscatter diffraction (ebsd) to study the microstructure of crystalline materials. - transmission imaging of thin samples using scanning transmission electron microscopy (stem) with dedicated detectors. - correlative microscopy by combining sem imaging with other techniques such as raman spectroscopy (rise microscopy) to gain complementary chemical and structural information. - automated workflows for imaging, analysis (e.g., particle analysis, non-metallic inclusion analysis), and in situ experiments to increase productivity and ensure reproducible results. - surface topography and 3d reconstruction using techniques like the annular bse detector (absd) and dedicated software to obtain quantitative information about the sample surface. - in situ experiments such as heating and tensile testing within the sem chamber to observe material behavior under controlled conditions. - failure analysis to investigate fractures, defects, and corrosion in various materials and components. - particle analysis for technical cleanliness and material characterization, including automated detection, measurement, counting, and classification of particles based on morphology and elemental composition. - quantitative mineralogy using automated sem and eds to classify mineral phases based on their chemical composition and provide detailed information on their properties."
]
embeddings = model.encode(sentences)
similarities = model.similarity(embeddings, embeddings)
print(similarities.shape)
# [4, 4]This is a sentence-transformers model finetuned from allenai/specter2_base. It maps sentences & paragraphs to a 768-dimensional dense vector space and can be used for semantic textual similarity, semantic search, paraphrase mining, text classification, clustering, and more.
SentenceTransformer(
(0): Transformer({'max_seq_length': 512, 'do_lower_case': False, 'architecture': 'BertModel'})
(1): Pooling({'word_embedding_dimension': 768, 'pooling_mode_cls_token': False, 'pooling_mode_mean_tokens': True, 'pooling_mode_max_tokens': False, 'pooling_mode_mean_sqrt_len_tokens': False, 'pooling_mode_weightedmean_tokens': False, 'pooling_mode_lasttoken': False, 'include_prompt': True})
)
First install the Sentence Transformers library:
pip install -U sentence-transformers
Then you can load this model and run inference.
from sentence_transformers import SentenceTransformer
# Download from the 🤗 Hub
model = SentenceTransformer("jagadeesh/zeiss-re-1757443344")
# Run inference
sentences = [
'We previously demonstrated that neural stem/progenitor cells (NSPCs) were induced within and around the ischemic areas in a mouse model of ischemic stroke. These injury/ischemia-induced NSPCs (iNSPCs) differentiated to electrophysiologically functional neurons in vitro, indicating the presence of a self-repair system following injury. However, during the healing process after stroke, ischemic areas were gradually occupied by inflammatory cells, mainly microglial cells/macrophages (MGs/MΦs), and neurogenesis rarely occurred within and around the ischemic areas. Therefore, to achieve neural regeneration by utilizing endogenous iNSPCs, regulation of MGs/MΦs after an ischemic stroke might be necessary. To test this hypothesis, we used iNSPCs isolated from the ischemic areas after a stroke in our mouse model to investigate the role of MGs/MΦs in iNSPC regulation. In coculture experiments, we show that the presence of MGs/MΦs significantly reduces not only the proliferation but also the differentiation of iNSPCs toward neuronal cells, thereby preventing neurogenesis. These effects, however, are mitigated by MG/MΦ depletion using clodronate encapsulated in liposomes. Additionally, gene ontology analysis reveals that proliferation and neuronal differentiation are negatively regulated in iNSPCs cocultured with MGs/MΦs. These results indicate that MGs/MΦs negatively impact neurogenesis via iNSPCs, suggesting that the regulation of MGs/MΦs is essential to achieve iNSPC-based neural regeneration following an ischemic stroke.',
"ZEISS Airyscan is an advanced imaging technology that enhances traditional confocal microscopy by using a 32-channel detector to capture more light with higher resolution and sensitivity. Unlike standard confocal systems that rely on a single pinhole, Airyscan collects the entire Airy disk pattern and reconstructs images for super-resolution clarityâ down to 120 nm laterally. This results in significantly improved signal-to-noise ratio and reduced photodamage, making it ideal for detailed imaging of live cells and biological samples. It's compatible with ZEISS LSM systems like the LSM 880 and 900, offering researchers a powerful tool for high-precision fluorescence microscopy",
"ZEISS Airyscan is an advanced imaging technology that enhances traditional confocal microscopy by using a 32-channel detector to capture more light with higher resolution and sensitivity. Unlike standard confocal systems that rely on a single pinhole, Airyscan collects the entire Airy disk pattern and reconstructs images for super-resolution clarityâ down to 120 nm laterally. This results in significantly improved signal-to-noise ratio and reduced photodamage, making it ideal for detailed imaging of live cells and biological samples. It's compatible with ZEISS LSM systems like the LSM 880 and 900, offering researchers a powerful tool for high-precision fluorescence microscopy",
]
embeddings = model.encode(sentences)
print(embeddings.shape)
# [3, 768]
# Get the similarity scores for the embeddings
similarities = model.similarity(embeddings, embeddings)
print(similarities)
# tensor([[1.0000, 0.6498, 0.6498],
# [0.6498, 1.0000, 1.0000],
# [0.6498, 1.0000, 1.0000]])
ir-evalInformationRetrievalEvaluator| Metric | Value |
|---|---|
| cosine_accuracy@1 | 0.1284 |
| cosine_accuracy@3 | 0.2932 |
| cosine_accuracy@5 | 0.4166 |
| cosine_accuracy@10 | 0.6476 |
| cosine_precision@1 | 0.1284 |
| cosine_precision@3 | 0.0977 |
| cosine_precision@5 | 0.0833 |
| cosine_precision@10 | 0.0648 |
| cosine_recall@1 | 0.1284 |
| cosine_recall@3 | 0.2932 |
| cosine_recall@5 | 0.4166 |
| cosine_recall@10 | 0.6476 |
| cosine_ndcg@10 | 0.3462 |
| cosine_mrr@10 | 0.2551 |
| cosine_map@100 | 0.2765 |
ir-evalInformationRetrievalEvaluator| Metric | Value |
|---|---|
| cosine_accuracy@1 | 0.1289 |
| cosine_accuracy@3 | 0.3094 |
| cosine_accuracy@5 | 0.4398 |
| cosine_accuracy@10 | 0.6926 |
| cosine_precision@1 | 0.1289 |
| cosine_precision@3 | 0.1031 |
| cosine_precision@5 | 0.088 |
| cosine_precision@10 | 0.0693 |
| cosine_recall@1 | 0.1289 |
| cosine_recall@3 | 0.3094 |
| cosine_recall@5 | 0.4398 |
| cosine_recall@10 | 0.6926 |
| cosine_ndcg@10 | 0.3646 |
| cosine_mrr@10 | 0.2655 |
| cosine_map@100 | 0.2837 |
ir-evalInformationRetrievalEvaluator| Metric | Value |
|---|---|
| cosine_accuracy@1 | 0.1274 |
| cosine_accuracy@3 | 0.2922 |
| cosine_accuracy@5 | 0.413 |
| cosine_accuracy@10 | 0.6355 |
| cosine_precision@1 | 0.1274 |
| cosine_precision@3 | 0.0974 |
| cosine_precision@5 | 0.0826 |
| cosine_precision@10 | 0.0635 |
| cosine_recall@1 | 0.1274 |
| cosine_recall@3 | 0.2922 |
| cosine_recall@5 | 0.413 |
| cosine_recall@10 | 0.6355 |
| cosine_ndcg@10 | 0.3426 |
| cosine_mrr@10 | 0.2538 |
| cosine_map@100 | 0.2748 |
ir-evalInformationRetrievalEvaluator| Metric | Value |
|---|---|
| cosine_accuracy@1 | 0.1795 |
| cosine_accuracy@3 | 0.4307 |
| cosine_accuracy@5 | 0.6062 |
| cosine_accuracy@10 | 0.8473 |
| cosine_precision@1 | 0.1795 |
| cosine_precision@3 | 0.1436 |
| cosine_precision@5 | 0.1212 |
| cosine_precision@10 | 0.0847 |
| cosine_recall@1 | 0.1795 |
| cosine_recall@3 | 0.4307 |
| cosine_recall@5 | 0.6062 |
| cosine_recall@10 | 0.8473 |
| cosine_ndcg@10 | 0.474 |
| cosine_mrr@10 | 0.3589 |
| cosine_map@100 | 0.3682 |
anchor and positive| anchor | positive | |
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| type | string | string |
| details |
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| anchor | positive |
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Nutrition and resilience are linked, though it is not yet clear how diet confers stress resistance or the breadth of stressors that it can protect against. We have previously shown that transiently restricting an essential amino acid can protect Drosophila melanogaster against nicotine poisoning. Here, we sought to characterize the nature of this dietary-mediated protection and determine whether it was sex, amino acid and/or nicotine specific. When we compared between sexes, we found that isoleucine deprivation increases female, but not male, nicotine resistance. Surprisingly, we found that this protection afforded to females was not replicated by dietary protein restriction and was instead specific to individual amino acid restriction. To understand whether these beneficial effects of diet were specific to nicotine or were generalizable across stressors, we pre-treated flies with amino acid restriction diets and exposed them to other types of stress. We found that some of the diets th... |
the zeiss stemi 508 is an apochromatic stereo microscope with an 8:1 zoom range, designed for high-contrast, color-accurate three-dimensional observation and documentation of diverse samples. its ergonomic design and robust mechanics support demanding applications in laboratory and industrial settings. key research and application areas: - biological research: suitable for observing the development and growth of model organisms like spider crabs, chicken, mouse, or zebrafish, including the evaluation, sorting, selection, or dissection of eggs, larvae, or embryos. it is also used in botany to observe changes in plant organs, diseases, and root development, in entomology for insect observation, documentation, and identification, in marine biology to study the life and reproduction of fish, and in parasitology for detecting and identifying the spread of parasites. the microscope is valuable for forensic analysis of ammunition parts, tool marks, documents, fibers, coatings, glass, textiles... |
The controlled supply of bioactive molecules is a subject of debate in animal nutrition. The release of bioactive molecules in the target organ, in this case the intestine, results in improved feed, as well as having a lower environmental impact. However, the degradation of bioactive molecules' in transit in the gastrointestinal passage is still an unresolved issue. This paper discusses the feasibility of a simple and cost-effective procedure to bypass the degradation problem. A solid/liquid adsorption procedure was applied, and the operating parameters (pH, reaction time, and LY initial concentration) were studied. Lysozyme is used in this work as a representative bioactive molecule, while Adsorbo ® , a commercial mixture of clay minerals and zeolites which meets current feed regulations, is used as the carrier. A maximum LY loading of 32 mg LY /g AD (LY(32)-AD) was obtained, with fixing pH in the range 7.5-8, initial LY content at 37.5 mg LY /g AD , and reaction time at 30 min. A ful... |
the zeiss evo family of scanning electron microscopes offers a modular and versatile platform for a wide range of scientific and industrial investigations, combining high-performance imaging and analysis with intuitive operation for users of varying experience levels. key research and application areas: - materials science: characterizing the morphology, structure, and composition of diverse materials, including metals, composites, polymers, ceramics, and coatings, for research and development. this includes investigating surface structures, fractures, inclusions, and grain boundaries. the evo supports advanced material analysis through techniques like energy dispersive spectroscopy (eds) and electron backscatter diffraction (ebsd). - life sciences: enabling the examination of biological specimens in their native or near-native hydrated states using variable and extended pressure modes. applications include imaging cells, tissues, plants, and microorganisms for structural and morpholog... |
Amorphous potassium sodium niobate (KNN) films were synthesized at 300 °C through the radio frequency magnetron sputtering method and subsequently crystallized by post-annealing at 700 °C in various alkali element atmospheres (Na and K). The as-deposited film is notably deficient in alkali metal elements, particularly K, whereas the loss of alkali elements in the films can be replenished through annealing in an alkali element atmosphere. By adjusting the molar ratio of Na and K in the annealing atmosphere, the ratio of Na/K in the resultant film varied, consequently suggesting the efficiency of this method on composition regulation of KNN films. Meanwhile, we also found that the physical characteristics of the films also underwent differences with the change of an annealing atmosphere. The films annealed in a high Na atmosphere exhibit large dielectric losses with limited piezoelectric vibration behavior, while annealing in a high K atmosphere reduces the dielectric losses and enhances... |
the zeiss sigma family of field emission scanning electron microscopes (fe-sems) offers versatile solutions for high-quality imaging and advanced analytical microscopy across a multitude of scientific and industrial domains. these instruments are engineered for reliable, high-end nano-analysis, combining fe-sem technology with an intuitive user experience to enhance productivity. key research and application areas: - advancing materials science: facilitating the development and understanding of novel materials by enabling the investigation of micro- and nanoscale structures. this includes characterizing metals, alloys, polymers, catalysts, and coatings for various applications such as electronics and energy. - driving innovation in nanoscience and nanomaterials: providing capabilities for the analysis of nanoparticles, thin films, 2d materials (like graphene and mos2), and other nanostructures to understand their properties and potential applications. - supporting energy research: enab... |
MultipleNegativesRankingLoss with these parameters:{
"scale": 20.0,
"similarity_fct": "cos_sim",
"gather_across_devices": false
}
eval_strategy: stepsper_device_train_batch_size: 64per_device_eval_batch_size: 64num_train_epochs: 5warmup_ratio: 0.1fp16: Truebatch_sampler: no_duplicatesoverwrite_output_dir: Falsedo_predict: Falseeval_strategy: stepsprediction_loss_only: Trueper_device_train_batch_size: 64per_device_eval_batch_size: 64per_gpu_train_batch_size: Noneper_gpu_eval_batch_size: Nonegradient_accumulation_steps: 1eval_accumulation_steps: Nonetorch_empty_cache_steps: Nonelearning_rate: 5e-05weight_decay: 0.0adam_beta1: 0.9adam_beta2: 0.999adam_epsilon: 1e-08max_grad_norm: 1.0num_train_epochs: 5max_steps: -1lr_scheduler_type: linearlr_scheduler_kwargs: {}warmup_ratio: 0.1warmup_steps: 0log_level: passivelog_level_replica: warninglog_on_each_node: Truelogging_nan_inf_filter: Truesave_safetensors: Truesave_on_each_node: Falsesave_only_model: Falserestore_callback_states_from_checkpoint: Falseno_cuda: Falseuse_cpu: Falseuse_mps_device: Falseseed: 42data_seed: Nonejit_mode_eval: Falseuse_ipex: Falsebf16: Falsefp16: Truefp16_opt_level: O1half_precision_backend: autobf16_full_eval: Falsefp16_full_eval: Falsetf32: Nonelocal_rank: 0ddp_backend: Nonetpu_num_cores: Nonetpu_metrics_debug: Falsedebug: []dataloader_drop_last: Falsedataloader_num_workers: 0dataloader_prefetch_factor: Nonepast_index: -1disable_tqdm: Falseremove_unused_columns: Truelabel_names: Noneload_best_model_at_end: Falseignore_data_skip: Falsefsdp: []fsdp_min_num_params: 0fsdp_config: {'min_num_params': 0, 'xla': False, 'xla_fsdp_v2': False, 'xla_fsdp_grad_ckpt': False}fsdp_transformer_layer_cls_to_wrap: Noneaccelerator_config: {'split_batches': False, 'dispatch_batches': None, 'even_batches': True, 'use_seedable_sampler': True, 'non_blocking': False, 'gradient_accumulation_kwargs': None}parallelism_config: Nonedeepspeed: Nonelabel_smoothing_factor: 0.0optim: adamw_torch_fusedoptim_args: Noneadafactor: Falsegroup_by_length: Falselength_column_name: lengthddp_find_unused_parameters: Noneddp_bucket_cap_mb: Noneddp_broadcast_buffers: Falsedataloader_pin_memory: Truedataloader_persistent_workers: Falseskip_memory_metrics: Trueuse_legacy_prediction_loop: Falsepush_to_hub: Falseresume_from_checkpoint: Nonehub_model_id: Nonehub_strategy: every_savehub_private_repo: Nonehub_always_push: Falsehub_revision: Nonegradient_checkpointing: Falsegradient_checkpointing_kwargs: Noneinclude_inputs_for_metrics: Falseinclude_for_metrics: []eval_do_concat_batches: Truefp16_backend: autopush_to_hub_model_id: Nonepush_to_hub_organization: Nonemp_parameters: auto_find_batch_size: Falsefull_determinism: Falsetorchdynamo: Noneray_scope: lastddp_timeout: 1800torch_compile: Falsetorch_compile_backend: Nonetorch_compile_mode: Noneinclude_tokens_per_second: Falseinclude_num_input_tokens_seen: Falseneftune_noise_alpha: Noneoptim_target_modules: Nonebatch_eval_metrics: Falseeval_on_start: Falseuse_liger_kernel: Falseliger_kernel_config: Noneeval_use_gather_object: Falseaverage_tokens_across_devices: Falseprompts: Nonebatch_sampler: no_duplicatesmulti_dataset_batch_sampler: proportionalrouter_mapping: {}learning_rate_mapping: {}| Epoch | Step | Training Loss | ir-eval_cosine_ndcg@10 |
|---|---|---|---|
| -1 | -1 | - | 0.1872 |
| 0.0898 | 100 | 2.488 | 0.2632 |
| 0.1797 | 200 | 2.321 | 0.3059 |
| 0.2695 | 300 | 2.0777 | 0.3453 |
| 0.3594 | 400 | 1.8331 | 0.3041 |
| 0.4492 | 500 | 1.7476 | 0.2957 |
| 0.5391 | 600 | 1.636 | 0.3263 |
| 0.6289 | 700 | 1.6187 | 0.3007 |
| 0.7188 | 800 | 1.4823 | 0.3403 |
| 0.8086 | 900 | 1.3278 | 0.2555 |
| 0.8985 | 1000 | 1.3049 | 0.2055 |
| 0.9883 | 1100 | 1.2643 | 0.2498 |
| 1.0782 | 1200 | 2.0728 | 0.3045 |
| 1.1680 | 1300 | 2.0786 | 0.3186 |
| 1.2579 | 1400 | 1.949 | 0.3343 |
| 1.3477 | 1500 | 1.7133 | 0.3402 |
| 1.4376 | 1600 | 1.6963 | 0.2970 |
| 1.5274 | 1700 | 1.5702 | 0.2728 |
| 1.6173 | 1800 | 1.5279 | 0.2667 |
| 1.7071 | 1900 | 1.3978 | 0.2342 |
| 1.7969 | 2000 | 1.2756 | 0.2354 |
| 1.8868 | 2100 | 1.1746 | 0.2236 |
| 1.9766 | 2200 | 1.2698 | 0.2443 |
| 2.0665 | 2300 | 1.8099 | 0.3395 |
| 2.1563 | 2400 | 1.8809 | 0.3456 |
| 2.2462 | 2500 | 1.826 | 0.3316 |
| 2.3360 | 2600 | 1.5636 | 0.3375 |
| 2.4259 | 2700 | 1.529 | 0.2894 |
| 2.5157 | 2800 | 1.4501 | 0.2816 |
| 2.6056 | 2900 | 1.3876 | 0.2782 |
| 2.6954 | 3000 | 1.3273 | 0.2772 |
| 2.7853 | 3100 | 1.1583 | 0.2810 |
| 2.8751 | 3200 | 1.1515 | 0.2856 |
| 2.9650 | 3300 | 1.1539 | 0.2849 |
| 3.0548 | 3400 | 1.5729 | 0.3380 |
| 3.1447 | 3500 | 1.6835 | 0.3462 |
| 3.2345 | 3600 | 1.5857 | 0.3533 |
| 3.3243 | 3700 | 1.4443 | 0.3462 |
| -1 | -1 | - | 0.3661 |
| 0.0898 | 100 | 1.7025 | 0.3527 |
| 0.1797 | 200 | 1.6829 | 0.3600 |
| 0.2695 | 300 | 1.6242 | 0.3649 |
| 0.3594 | 400 | 1.5047 | 0.3614 |
| 0.4492 | 500 | 1.4711 | 0.3793 |
| 0.5391 | 600 | 1.4528 | 0.3646 |
| -1 | -1 | - | 0.3183 |
| 0.3584 | 100 | 1.823 | 0.3093 |
| 0.7168 | 200 | 1.8014 | 0.3297 |
| 1.0753 | 300 | 1.8726 | 0.3504 |
| 1.4337 | 400 | 1.7708 | 0.3233 |
| 1.7921 | 500 | 1.5537 | 0.3210 |
| 2.1505 | 600 | 1.6994 | 0.3996 |
| 2.5090 | 700 | 1.3569 | 0.3240 |
| 2.8674 | 800 | 1.369 | 0.3325 |
| 3.2258 | 900 | 1.3097 | 0.4251 |
| 3.5842 | 1000 | 1.1224 | 0.3971 |
| 3.9427 | 1100 | 1.2093 | 0.4377 |
| 4.3011 | 1200 | 1.012 | 0.4723 |
| 4.6595 | 1300 | 1.0207 | 0.4740 |
@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",
}
@misc{henderson2017efficient,
title={Efficient Natural Language Response Suggestion for Smart Reply},
author={Matthew Henderson and Rami Al-Rfou and Brian Strope and Yun-hsuan Sung and Laszlo Lukacs and Ruiqi Guo and Sanjiv Kumar and Balint Miklos and Ray Kurzweil},
year={2017},
eprint={1705.00652},
archivePrefix={arXiv},
primaryClass={cs.CL}
}
Base model
allenai/specter2_base