---
language:
- en
tags:
- sentence-transformers
- sentence-similarity
- feature-extraction
- dense
- generated_from_trainer
- dataset_size:70764
- loss:MultipleNegativesRankingLoss
base_model: sentence-transformers/allenai-specter
widget:
- source_sentence: The hyperspace ω(f) when f is a transitive dendrite mapping
sentences:
- 'Knee osteoarthritis (OA) is a major cause of chronic pain and disability in older
adults, yet scalable home-based interventions remain limited, partly due to the
lack of clinically effective digital solutions. This study is the first fully
powered randomized, double-blind, sham-controlled trial to test a digitally delivered,
home-based protocol combining transcranial direct current stimulation (tDCS) and
mindfulness-based meditation (MBM) for knee OA pain. A total of 208 participants
were randomized to active tDCS + MBM, active tDCS + sham MBM, sham tDCS + active
MBM, or double sham; they completed ten 20-min sessions over 2 weeks. Knee pain
intensity was measured at baseline, post treatment, and monthly for 3 months.
Although both active tDCS groups improved, the difference between the combined
tDCS + MBM intervention and tDCS alone was not statistically significant. Benefits
were not sustained at 3 months. These findings offer the first evidence that a
remotely supervised, digitally delivered tDCS + MBM intervention can rapidly reduce
knee OA pain, supporting future personalized and extended treatment studies. Clinical
trial registration: ClinicalTrials.gov NCT04375072 (registered May 7, 2020).'
- ' Let $X$ be a compact metric space. By $2^X$ we denote the hyperspace of all
closed and non-empty subsets of $X$ endowed with the Hausdorff metric. Let
$f:X\to X$ be a continuous function. In this paper we study some topological
properties of the hyperspace $\omega(f)$, the collection of all omega limits
sets $\omega(x,f)$ with $x\in X$. We prove the following: $i)$ If $X$ has no
isolated points, then, for every continuous function $f:X\to X$,
$int_{2^X}(\omega(f))=\emptyset$. $ii)$ If $X$ is a dendrite for which every
arc contains a free arc and $f:X\to X$ is transitive, then the hyperspace
$\omega(f)$ is totally disconnected. $iii)$ Let $D_\infty$ be the Wazewski''s
universal dendrite. Then there exists a transitive continuous function
$f:D_\infty\to D_\infty$ for which the hyperspace $\omega(f)$ contains an arc;
hence, $\omega(f)$ is not totally disconnected.
'
- Let $X_1,\,X_2,\,\ldots,\,X_N$, $N\in\mathbb N$ be independent, discrete, integer-valued
random variables. Assume that $X_j\geqslant m_j$ almost surely for each $j=1,\,2,\,\ldots,\,N$,
where $m_1,\,m_2,\,\ldots,\,m_N\in\mathbb{Z}$ satisfy $m_1+\cdots+m_N<0$. Furthermore,
suppose that the sequence $X_1,\,X_2,\,\ldots$ is periodic in distribution, i.e.
$X_k{\buildrel d \over =} X_{k+N}$ for all $k\in\mathbb N$. We derive computable
representations for the distribution functions of $\max\{X_1,\,X_1+X_2,\,\ldots\}$,
$\max\{X_2,\,X_2+X_3,\,\ldots\}$, $\ldots$, $\max\{X_N,\,X_N+X_{N+1},\,\ldots\}$.
The obtained formulas are based on a linear recurrence whose initial values are
determined from a linear system that involves the roots of an associated characteristic
equation and the distributions of $X_1,\,X_2,\,\ldots,\,X_N$. Several examples
are presented, including a biseasonal-biased Rademacher random walk for which
the distribution, generating functions, and all moments admit explicit closed-form
expressions. In addition, we identify and correct several inaccuracies in the
results reported in \cite{Grigutis2024}.
- source_sentence: New mechanism for delayed ENSO impact on the East Asian Summer
Monsoon
sentences:
- Abstract Due to its potentially life—threatening and devastating economic impacts,
variability in the East Asian Summer Monsoon needs better understanding, more
accurate simulation and improved prediction. Much of the current ability of long-range
summer monsoon forecasts stems from the link to the preceding winter El Niño Southern
Oscillation, but the mechanisms behind this lagged impact are not fully understood.
In this study, a simple new mechanism is proposed, based on migrating Atmospheric
Angular Momentum anomalies. The polewards migration of atmospheric angular momentum
associated with winter El Niño is shown to impact the northwest Pacific anticyclone
responsible for much of the year-to-year variability in the monsoon. Model forecasts
of the summer monsoon are shown to have increased accuracy when this new mechanism
is active, with the increase in the success rate of forecasts due to migrating
angular momentum anomalies shown to be as large as the effect of El Niño itself.
- 'Automated algorithm selection in black-box optimization typically relies on supervised
models that map landscape features to algorithm performance labels. Such models
are costly to train, benchmark-dependent, and often fail to generalize to unseen
problem classes. We study an unsupervised alternative: multi-kernel clustering
over heterogeneous landscape representations, in which problem instances are grouped
without using performance labels in the clustering stage, and the resulting clusters
are mapped post hoc to solver recommendations through a strictly separated three-stage
evaluation protocol. Drawing on two decades of advances in multiple kernel learning,
we adopt a multi-kernel k-means formulation that jointly learns cluster assignments
and kernel weights over four heterogeneous landscape views: ELA, DeepELA, DoE2Vec,
and TransOptAS. On affine BBOB-derived selector tasks for Differential Evolution
(DE) and Particle Swarm Optimization (PSO) at a fixed evaluation budget, we report
mean plus or minus standard deviation selector profiles over 50 independent random
seeds for stochastic configurations. Multi-kernel clustering obtains the strongest
mean profile on the DE portfolio and remains competitive with, and nominally ahead
of, the leading baselines on the more compressed PSO portfolio, where differences
among the best methods are small relative to stochastic variation. In representative
median-seed runs used for visualization, the learned kernel weights retain ELA
and TransOptAS while assigning zero weight to DeepELA and DoE2Vec, providing a
task-specific interpretation of which representations are retained by the multi-kernel
model for selector-oriented grouping.'
- Prolonged social isolation (SI) and negative emotion are associated with an increased
risk of cardiovascular diseases (CVDs). However, it remains elusive whether SI
and emotional states affect the pathological process of myocardial infarction
(MI). In this study, SI models with different duration and MI model were co-established
in mice. Anxiety and depression were assessed by a series of behavioral tests
including open field test, elevated plus maze test, novelty-suppressed feeding
test, tail suspension test and forced swim test. Cardiac function, heart infarct
size and fibrosis were assessed by echocardiography, TTC staining, and Masson
staining. The activity of neurons across the whole brain, as well as the hypothalamic-pituitary-adrenal
(HPA) axis, was also investigated. Long-term SI induced anxiety and depression-like
behaviors and aggravated cardiac injury and inflammatory response in MI mice,
while short-term SI induced anxiety-like behavior but not depression-like behavior
and had no significant effects on cardiac injury. Long-term SI altered the activity
of several brain regions related to emotional, reward, autonomic and neuroendocrine
regulation in MI mice. Furthermore, serum corticosterone levels were altered,
indicating the potential involvement of HPA axis. These findings reveal that long-term
SI exacerbated cardiac dysfunction and cardiac injury after MI. The underlying
mechanisms involved in this process may include negative mood, dysregulation of
the reward system, autonomic nervous system modulation, and HPA axis activation.
These findings will contribute to our better understanding of heart-brain connections.
- source_sentence: Towards a Theory of Dobrakov-Sobolev Spaces
sentences:
- The aim of this paper is to introduce a generalization of Sobolev spaces based
on the Dobrakov integral. More precisely, we consider the setting of Banach-valued
functions and Fomin differentiable Borel operator-valued measures on a finite-dimensional
space. To build the necessary rigorous foundation, we establish analogs of several
key results from the theory of differentiable real-valued measures, including
the Leibniz rule and the integration by parts formula, all within the context
of Dobrakov integration. These results are then embedded into the general scheme
of vector-valued distribution theory. In particular, we describe the configuration
of test spaces that yields an appropriate definition of a generalized derivative
with respect to a differentiable operator-valued measure.
- AI agents are increasingly used to automate research and development tasks, yet
existing benchmarks typically evaluate them on prescribed workflows or narrow
action spaces. Even nominally open-ended tasks can often be solved by retrieving
a well-known recipe and tuning a few hyperparameters, making it unclear whether
strong results reflect genuine optimization or memorized solutions. We introduce
InferenceBench, where an agent must deploy an OpenAI-compatible inference server
and optimize the speed of LLM inference. Each agent receives a target LLM, one
H100 GPU, an optimization scenario, and a wall-clock time budget of two hours.
Three optimization scenarios isolate distinct bottlenecks of inference (prefill
latency, decode latency, and concurrent request throughput) and a fourth balances
all three at the same time. Across 15 frontier agent configurations, agents reliably
improve over a naive PyTorch baseline (up to $8.08\times$) and often match or
exceed serving engines with default settings ($4.05\times$ for vLLM), but still
fall below a simple hyperparameter search under the same time budget (up to $11.53\times$).
Qualitative analysis of agent trajectories shows that although agents enumerate
many relevant optimization techniques, they overwhelmingly converge on a single
inference framework. They test only a few distinct configurations and spend the
remaining budget re-measuring, repairing, or optimizing hyperparameters rather
than exploring substantially different strategies. This suggests the bottleneck
is not domain knowledge, but the ability to propose diverse configurations, evaluate
them systematically, and submit the best identified solution. Overall, InferenceBench
reflects the ability of agents to operate in an open-ended AI engineering setting,
where memorized solutions lead to limited improvements.
- Abstract Patients with multiple myeloma bearing a deletion of chromosome 17p (del(17p)),
mutation of TP53 , or both have poorer prognosis compared to patients without
these aberrations. We investigated the activity and mechanism of melflufen (melphalan
flufenamide) in myeloma models with wild type TP53 ( TP53 wt) and complete TP53
deletion ( TP53 −/− ) and assessed the efficacy of melflufen in patients with
del(17p) and/or TP53 mutation. Ex vivo data from myeloma plasma cells (PC) showed
comparable activity of melflufen in del(17p), TP53 −/− , and TP53 wt samples.
scRNAseq data demonstrated that melflufen sensitive PCs had lower expression of
p53 target genes and higher expression of genes associated with DNA damage repair
and cell cycle checkpoints. Irrespective of TP53 status, melflufen induced apoptosis,
DNA damage, and mitochondrial dysfunction, while only in TP53 −/− cells, it led
to changes in expression of cell cycle checkpoint and apoptosis genes. Post-hoc
analysis of the OCEAN trial melflufen-treated del(17p) patient population also
demonstrated favorable progression free survival compared to pomalidomide-treated
cohort. Our insights into the molecular mechanisms of melflufen activity in TP53
−/− myeloma support its clinical efficacy and application in the del(17p) and
TP53 −/− patient population. Trial registration NCT03151811, registration 2017-05-09.
- source_sentence: 'Strengthening complexity in EU: the role of educational policy
and R&D spending'
sentences:
- The drivers of economic complexity in the countries of the European Union (EU)
are a question of significant importance, especially in the context of the emergence
of a trade war. Studying the relationship between economic complexity and macroeconomic,
educational and technological variables, we offer valuable conclusions for the
design and formulation of new policies. The Economic Complexity Index (ECI) is
analysed in the context of education expenditure, gross fixed capital formation,
fiscal balance, R&D expenditure, and patent applications, using relevant econometric
techniques such as the 3SLS and the SURE analysis. Education expenditures are
found to affect significantly the Economic Complexity of a country. Moreover,
after the outburst of the sovereign-debt crisis the fiscal balance has become
a prerequisite for all European countries, showing a positive relationship with
economic complexity. This result poses the question of how weaker economies can
finance the necessary policies to increase their economic complexity, such as
raising spending on education, R&D, and fixed capital investment, while maintaining
fiscal stability.
- 'Proxy metrics are widely used to improve the precision and velocity of online
experimentation (aka A/B testing). Although proxies are often motivated by long-term
outcomes that the experimenter does not observe, in many settings they are used
alongside a contemporaneous but statistically insensitive north star. This can
lead to a practical dilemma: when should experimenters trust the proxy metric,
and when should they trust the north star? In this paper, I propose an optimal
blending approach that smoothly guides decision-making towards the north star
as the power of the experiment increases and away from the north star as the quality
of the proxy metric improves. I study the implications of this decision-making
framework for the design of experiments and of experimentation programs. Equipped
with better (worse) proxy metrics, experimenters should run smaller and more (larger
and fewer) experiments. I show how to leverage past experiments to estimate optimal
blending weights and experiment sizes. Lastly, I describe the real-world application
of the methodology to an experimentation program at Netflix.'
- We consider a quenched SU(2)$\times$U(1) gauge Higgs theory on the lattice, coupled
to a static vector-like fermion which, in this case, is in the same gauge group
representation as the Higgs field. Physical (i.e. locally gauge invariant) electrically
charged and electrically neutral states of matter particles in the electroweak
theory were described decades ago, but those constructions do not exhaust all
the possibilities, and new types of electrically charged/neutral states, orthogonal
to former constructions, are described here. The difference has to do with how
the static source, which by itself does not create a physical state, is dressed
by dynamical fields. We find that, unsurprisingly, the neutral static fermion
is much lighter than any of the charged fermion states. But a lattice study of
the propagation of the charged fermion states indicates the existence of (at least)
two particle states with different masses in charged particle spectrum.
- source_sentence: ERBB3 blockade sensitizes hepatocellular carcinoma to regorafenib
after first-line tyrosine kinase inhibitor resistance by inhibiting HIF1A-ABCB1
signaling
sentences:
- We improve the theoretical predictions for rare $Z$-boson decays, $Z\to V\ell^+\ell^-$
($\ell=e$ or $\mu$), where $V$ denotes a heavy vector quarkonium including $J/\Psi$,
$\Psi (2S)$, and $\Upsilon (nS)$ with $n=1,2,3$. These processes are thought to
be dominated by the electromagnetic fragmentation transition, i.e., $Z\to \gamma^*\ell^+\ell^-$
followed by $\gamma^*\rightarrow V$. The present study includes all of the relevant
tree-level Feynman diagrams, which contribute to these decays in the standard
model. Our analysis shows that, for the charmonium final states, the fragmentation
transition almost saturates the whole contribution and the other diagrams can
be neglected; while for the bottomonium final states, the inclusion of other diagrams
can increase their branching fractions by $4\%\sim 9\%$. Further investigation
of the differential distributions, especially the angular distributions, indicates
that forward-backward asymmetries for final leptons in these processes would be
zero in the standard model. Therefore, in future experimental facilities with
large number of $Z$-boson events accumulated, studies of these rare $Z$ decays
may help both to test the standard model and to probe its interesting extensions.
- 'Historically, veterinary studies screening for breed, age and sex predisposition
to disease have relied on collating small-scale studies of clinical datasets.
The availability of larger datasets through groups such as the Small Animal Veterinary
Surveillance Network (SAVSNET) promise access to information regarding a wide
range of clinical presentations at scale, however, methodological limitations
surrounding the extraction of specific disease information or screening for disease
predispositions result in a substantial reduction in the number of animals studied.
These studies often address very focused hypotheses - only leveraging a small
fraction of the intrinsic value of the data at any one time. Here, we implemented
an unsupervised machine learning methodology, creating a representation of a large
volume of clinical notes collected by SAVSNET from veterinary practices across
the UK. We utilise BERTopic, a topic-modelling tool based on Bidirectional Encoder
Representations using Transformers (BERT) architecture, and show it is able to
surface known phenotypes, such as breed predispositions to hypoadrenocorticism,
diabetes mellitus and mitral valve disease, as well as potential novel patterns
of disease phenotypes. This scalable and granular modelling technique facilitates
the rapid interrogation of large clinical datasets, enabling the identification
of a broad range of phenotypes within the population and the early detection of
temporal changes indicative of emerging infectious or environmental diseases.
Supplementary Information: The online version contains supplementary material
available at 10.1186/s40537-026-01365-0.'
- 'BACKGROUND/AIMS: Regorafenib is recommended by guidelines and trials as a sequential
second-line therapy following progression on first-line sorafenib or lenvatinib
in hepatocellular carcinoma (HCC). However, efficacy is limited, highlighting
the urgent need to screen suitable patients and develop sensitization strategies.
METHODS: Acquired sorafenib- or lenvatinib-resistant (SR or LR) HCC cell lines
and organoids were established. Genome-wide CRISPR library screen was performed
in SR or LR cell strains to identify synthetic lethal targets of regorafenib.
RNA-seq and FITC-regorafenib efflux assay were used to elucidate ERBB3-driven
downstream signaling. Preclinical mouse models of cell line- and patient-derived
xenografts and clinical cohorts of HCC patients were employed to validate the
efficacy of ERBB3-guided patient stratification. RESULTS: Screening with CRISPR
library, we showed that inhibition of ERBB3 was synthetic lethal with regorafenib
in SR or LR cell strains and organoids. Mechanistically, SR or LR triggered feedback
activation of ERBB3 signaling and mediated regorafenib efflux via ERBB3-HIF1A-ABCB1
cascade pathway, limiting sensitivity to regorafenib. Moreover, ERBB3-low tumors
following SR or LR exhibited significant sensitivity to regorafenib, suggesting
its potential as a predictive biomarker to screen optimal candidates for sequential
therapy. Seribantumab, an ERBB3-targeting monoclonal antibody, inhibited ERBB3-HIF1A-ABCB1
cascade, and its combination with regorafenib exerted marked synergistic anti-tumor
effects on ERBB3-high tumors resistant to sorafenib or lenvatinib both in vitro
and in vivo. CONCLUSIONS: This study revealed that ERBB3 was a key resistance
factor driving limited efficacy to sequential regorafenib, but also an effective
therapeutic target whose inhibition enhanced regorafenib sensitivity after SR
or LR.'
pipeline_tag: sentence-similarity
library_name: sentence-transformers
metrics:
- cosine_accuracy@1
- cosine_accuracy@3
- cosine_accuracy@5
- cosine_accuracy@10
- cosine_precision@1
- cosine_precision@3
- cosine_precision@5
- cosine_precision@10
- cosine_recall@1
- cosine_recall@3
- cosine_recall@5
- cosine_recall@10
- cosine_ndcg@10
- cosine_mrr@10
- cosine_map@100
model-index:
- name: chowder-embed (SPECTER fine-tuned on the chowder corpus)
results:
- task:
type: information-retrieval
name: Information Retrieval
dataset:
name: NanoSCIDOCS
type: NanoSCIDOCS
metrics:
- type: cosine_accuracy@1
value: 0.38
name: Cosine Accuracy@1
- type: cosine_accuracy@3
value: 0.62
name: Cosine Accuracy@3
- type: cosine_accuracy@5
value: 0.72
name: Cosine Accuracy@5
- type: cosine_accuracy@10
value: 0.86
name: Cosine Accuracy@10
- type: cosine_precision@1
value: 0.38
name: Cosine Precision@1
- type: cosine_precision@3
value: 0.31333333333333335
name: Cosine Precision@3
- type: cosine_precision@5
value: 0.256
name: Cosine Precision@5
- type: cosine_precision@10
value: 0.176
name: Cosine Precision@10
- type: cosine_recall@1
value: 0.08066666666666666
name: Cosine Recall@1
- type: cosine_recall@3
value: 0.19466666666666665
name: Cosine Recall@3
- type: cosine_recall@5
value: 0.26266666666666666
name: Cosine Recall@5
- type: cosine_recall@10
value: 0.3616666666666666
name: Cosine Recall@10
- type: cosine_ndcg@10
value: 0.3456136739010105
name: Cosine Ndcg@10
- type: cosine_mrr@10
value: 0.534436507936508
name: Cosine Mrr@10
- type: cosine_map@100
value: 0.26477117793177524
name: Cosine Map@100
- task:
type: information-retrieval
name: Information Retrieval
dataset:
name: NanoSciFact
type: NanoSciFact
metrics:
- type: cosine_accuracy@1
value: 0.6
name: Cosine Accuracy@1
- type: cosine_accuracy@3
value: 0.68
name: Cosine Accuracy@3
- type: cosine_accuracy@5
value: 0.72
name: Cosine Accuracy@5
- type: cosine_accuracy@10
value: 0.8
name: Cosine Accuracy@10
- type: cosine_precision@1
value: 0.6
name: Cosine Precision@1
- type: cosine_precision@3
value: 0.24666666666666665
name: Cosine Precision@3
- type: cosine_precision@5
value: 0.16
name: Cosine Precision@5
- type: cosine_precision@10
value: 0.09
name: Cosine Precision@10
- type: cosine_recall@1
value: 0.565
name: Cosine Recall@1
- type: cosine_recall@3
value: 0.67
name: Cosine Recall@3
- type: cosine_recall@5
value: 0.715
name: Cosine Recall@5
- type: cosine_recall@10
value: 0.79
name: Cosine Recall@10
- type: cosine_ndcg@10
value: 0.6831330092247734
name: Cosine Ndcg@10
- type: cosine_mrr@10
value: 0.6557142857142857
name: Cosine Mrr@10
- type: cosine_map@100
value: 0.6496795415115648
name: Cosine Map@100
- task:
type: information-retrieval
name: Information Retrieval
dataset:
name: NanoNFCorpus
type: NanoNFCorpus
metrics:
- type: cosine_accuracy@1
value: 0.3
name: Cosine Accuracy@1
- type: cosine_accuracy@3
value: 0.36
name: Cosine Accuracy@3
- type: cosine_accuracy@5
value: 0.46
name: Cosine Accuracy@5
- type: cosine_accuracy@10
value: 0.54
name: Cosine Accuracy@10
- type: cosine_precision@1
value: 0.3
name: Cosine Precision@1
- type: cosine_precision@3
value: 0.2533333333333333
name: Cosine Precision@3
- type: cosine_precision@5
value: 0.248
name: Cosine Precision@5
- type: cosine_precision@10
value: 0.222
name: Cosine Precision@10
- type: cosine_recall@1
value: 0.012486154892961041
name: Cosine Recall@1
- type: cosine_recall@3
value: 0.0309389720826588
name: Cosine Recall@3
- type: cosine_recall@5
value: 0.047390511275329145
name: Cosine Recall@5
- type: cosine_recall@10
value: 0.10215743728341801
name: Cosine Recall@10
- type: cosine_ndcg@10
value: 0.24495153881224493
name: Cosine Ndcg@10
- type: cosine_mrr@10
value: 0.3605714285714285
name: Cosine Mrr@10
- type: cosine_map@100
value: 0.09185350554401533
name: Cosine Map@100
- task:
type: nano-beir
name: Nano BEIR
dataset:
name: NanoBEIR mean
type: NanoBEIR_mean
metrics:
- type: cosine_accuracy@1
value: 0.4266666666666667
name: Cosine Accuracy@1
- type: cosine_accuracy@3
value: 0.5533333333333333
name: Cosine Accuracy@3
- type: cosine_accuracy@5
value: 0.6333333333333333
name: Cosine Accuracy@5
- type: cosine_accuracy@10
value: 0.7333333333333334
name: Cosine Accuracy@10
- type: cosine_precision@1
value: 0.4266666666666667
name: Cosine Precision@1
- type: cosine_precision@3
value: 0.27111111111111114
name: Cosine Precision@3
- type: cosine_precision@5
value: 0.22133333333333335
name: Cosine Precision@5
- type: cosine_precision@10
value: 0.16266666666666665
name: Cosine Precision@10
- type: cosine_recall@1
value: 0.21938427385320922
name: Cosine Recall@1
- type: cosine_recall@3
value: 0.29853521291644186
name: Cosine Recall@3
- type: cosine_recall@5
value: 0.3416857259806653
name: Cosine Recall@5
- type: cosine_recall@10
value: 0.4179413679833615
name: Cosine Recall@10
- type: cosine_ndcg@10
value: 0.42456607397934293
name: Cosine Ndcg@10
- type: cosine_mrr@10
value: 0.5169074074074074
name: Cosine Mrr@10
- type: cosine_map@100
value: 0.33543474166245174
name: Cosine Map@100
- task:
type: information-retrieval
name: Information Retrieval
dataset:
name: chowder val
type: chowder-val
metrics:
- type: cosine_accuracy@1
value: 0.952
name: Cosine Accuracy@1
- type: cosine_accuracy@3
value: 0.9805
name: Cosine Accuracy@3
- type: cosine_accuracy@5
value: 0.989
name: Cosine Accuracy@5
- type: cosine_accuracy@10
value: 0.9955
name: Cosine Accuracy@10
- type: cosine_precision@1
value: 0.952
name: Cosine Precision@1
- type: cosine_precision@3
value: 0.32683333333333325
name: Cosine Precision@3
- type: cosine_precision@5
value: 0.1978
name: Cosine Precision@5
- type: cosine_precision@10
value: 0.09955000000000001
name: Cosine Precision@10
- type: cosine_recall@1
value: 0.952
name: Cosine Recall@1
- type: cosine_recall@3
value: 0.9805
name: Cosine Recall@3
- type: cosine_recall@5
value: 0.989
name: Cosine Recall@5
- type: cosine_recall@10
value: 0.9955
name: Cosine Recall@10
- type: cosine_ndcg@10
value: 0.9743050654346748
name: Cosine Ndcg@10
- type: cosine_mrr@10
value: 0.9674267857142853
name: Cosine Mrr@10
- type: cosine_map@100
value: 0.9676369980648283
name: Cosine Map@100
---
# chowder-embed (SPECTER fine-tuned on the chowder corpus)
This is a [sentence-transformers](https://www.SBERT.net) model finetuned from [sentence-transformers/allenai-specter](https://huggingface.co/sentence-transformers/allenai-specter) on the parquet dataset. It maps sentences & paragraphs to a 768-dimensional dense vector space and can be used for semantic textual similarity, semantic search, paraphrase mining, classification, clustering, and more.
## Model Details
### Model Description
- **Model Type:** Sentence Transformer
- **Base model:** [sentence-transformers/allenai-specter](https://huggingface.co/sentence-transformers/allenai-specter)
- **Maximum Sequence Length:** 512 tokens
- **Output Dimensionality:** 768 dimensions
- **Similarity Function:** Cosine Similarity
- **Supported Modality:** Text
- **Training Dataset:**
- parquet
- **Language:** en
### Model Sources
- **Documentation:** [Sentence Transformers Documentation](https://sbert.net)
- **Repository:** [Sentence Transformers on GitHub](https://github.com/huggingface/sentence-transformers)
- **Hugging Face:** [Sentence Transformers on Hugging Face](https://huggingface.co/models?library=sentence-transformers)
### Full Model Architecture
```
SentenceTransformer(
(0): Transformer({'transformer_task': 'feature-extraction', 'modality_config': {'text': {'method': 'forward', 'method_output_name': 'last_hidden_state'}}, 'module_output_name': 'token_embeddings', 'architecture': 'BertModel'})
(1): Pooling({'embedding_dimension': 768, 'pooling_mode': 'cls', 'include_prompt': True})
)
```
## Usage
### Direct Usage (Sentence Transformers)
First install the Sentence Transformers library:
```bash
pip install -U sentence-transformers
```
Then you can load this model and run inference.
```python
from sentence_transformers import SentenceTransformer
# Download from the 🤗 Hub
model = SentenceTransformer("Wakeleyhuh/chowder-embed-specter")
# Run inference
queries = [
'ERBB3 blockade sensitizes hepatocellular carcinoma to regorafenib after first-line tyrosine kinase inhibitor resistance by inhibiting HIF1A-ABCB1 signaling',
]
documents = [
'BACKGROUND/AIMS: Regorafenib is recommended by guidelines and trials as a sequential second-line therapy following progression on first-line sorafenib or lenvatinib in hepatocellular carcinoma (HCC). However, efficacy is limited, highlighting the urgent need to screen suitable patients and develop sensitization strategies. METHODS: Acquired sorafenib- or lenvatinib-resistant (SR or LR) HCC cell lines and organoids were established. Genome-wide CRISPR library screen was performed in SR or LR cell strains to identify synthetic lethal targets of regorafenib. RNA-seq and FITC-regorafenib efflux assay were used to elucidate ERBB3-driven downstream signaling. Preclinical mouse models of cell line- and patient-derived xenografts and clinical cohorts of HCC patients were employed to validate the efficacy of ERBB3-guided patient stratification. RESULTS: Screening with CRISPR library, we showed that inhibition of ERBB3 was synthetic lethal with regorafenib in SR or LR cell strains and organoids. Mechanistically, SR or LR triggered feedback activation of ERBB3 signaling and mediated regorafenib efflux via ERBB3-HIF1A-ABCB1 cascade pathway, limiting sensitivity to regorafenib. Moreover, ERBB3-low tumors following SR or LR exhibited significant sensitivity to regorafenib, suggesting its potential as a predictive biomarker to screen optimal candidates for sequential therapy. Seribantumab, an ERBB3-targeting monoclonal antibody, inhibited ERBB3-HIF1A-ABCB1 cascade, and its combination with regorafenib exerted marked synergistic anti-tumor effects on ERBB3-high tumors resistant to sorafenib or lenvatinib both in vitro and in vivo. CONCLUSIONS: This study revealed that ERBB3 was a key resistance factor driving limited efficacy to sequential regorafenib, but also an effective therapeutic target whose inhibition enhanced regorafenib sensitivity after SR or LR.',
'We improve the theoretical predictions for rare $Z$-boson decays, $Z\\to V\\ell^+\\ell^-$ ($\\ell=e$ or $\\mu$), where $V$ denotes a heavy vector quarkonium including $J/\\Psi$, $\\Psi (2S)$, and $\\Upsilon (nS)$ with $n=1,2,3$. These processes are thought to be dominated by the electromagnetic fragmentation transition, i.e., $Z\\to \\gamma^*\\ell^+\\ell^-$ followed by $\\gamma^*\\rightarrow V$. The present study includes all of the relevant tree-level Feynman diagrams, which contribute to these decays in the standard model. Our analysis shows that, for the charmonium final states, the fragmentation transition almost saturates the whole contribution and the other diagrams can be neglected; while for the bottomonium final states, the inclusion of other diagrams can increase their branching fractions by $4\\%\\sim 9\\%$. Further investigation of the differential distributions, especially the angular distributions, indicates that forward-backward asymmetries for final leptons in these processes would be zero in the standard model. Therefore, in future experimental facilities with large number of $Z$-boson events accumulated, studies of these rare $Z$ decays may help both to test the standard model and to probe its interesting extensions.',
'Historically, veterinary studies screening for breed, age and sex predisposition to disease have relied on collating small-scale studies of clinical datasets. The availability of larger datasets through groups such as the Small Animal Veterinary Surveillance Network (SAVSNET) promise access to information regarding a wide range of clinical presentations at scale, however, methodological limitations surrounding the extraction of specific disease information or screening for disease predispositions result in a substantial reduction in the number of animals studied. These studies often address very focused hypotheses - only leveraging a small fraction of the intrinsic value of the data at any one time. Here, we implemented an unsupervised machine learning methodology, creating a representation of a large volume of clinical notes collected by SAVSNET from veterinary practices across the UK. We utilise BERTopic, a topic-modelling tool based on Bidirectional Encoder Representations using Transformers (BERT) architecture, and show it is able to surface known phenotypes, such as breed predispositions to hypoadrenocorticism, diabetes mellitus and mitral valve disease, as well as potential novel patterns of disease phenotypes. This scalable and granular modelling technique facilitates the rapid interrogation of large clinical datasets, enabling the identification of a broad range of phenotypes within the population and the early detection of temporal changes indicative of emerging infectious or environmental diseases. Supplementary Information: The online version contains supplementary material available at 10.1186/s40537-026-01365-0.',
]
query_embeddings = model.encode_query(queries)
document_embeddings = model.encode_document(documents)
print(query_embeddings.shape, document_embeddings.shape)
# [1, 768] [3, 768]
# Get the similarity scores for the embeddings
similarities = model.similarity(query_embeddings, document_embeddings)
print(similarities)
# tensor([[0.8640, 0.0814, 0.0283]])
```
## Evaluation
### Metrics
#### Information Retrieval
* Datasets: `NanoSCIDOCS`, `NanoSciFact`, `NanoNFCorpus` and `chowder-val`
* Evaluated with [InformationRetrievalEvaluator](https://sbert.net/docs/package_reference/sentence_transformer/evaluation.html#sentence_transformers.sentence_transformer.evaluation.InformationRetrievalEvaluator)
| Metric | NanoSCIDOCS | NanoSciFact | NanoNFCorpus | chowder-val |
|:--------------------|:------------|:------------|:-------------|:------------|
| cosine_accuracy@1 | 0.38 | 0.6 | 0.3 | 0.952 |
| cosine_accuracy@3 | 0.62 | 0.68 | 0.36 | 0.9805 |
| cosine_accuracy@5 | 0.72 | 0.72 | 0.46 | 0.989 |
| cosine_accuracy@10 | 0.86 | 0.8 | 0.54 | 0.9955 |
| cosine_precision@1 | 0.38 | 0.6 | 0.3 | 0.952 |
| cosine_precision@3 | 0.3133 | 0.2467 | 0.2533 | 0.3268 |
| cosine_precision@5 | 0.256 | 0.16 | 0.248 | 0.1978 |
| cosine_precision@10 | 0.176 | 0.09 | 0.222 | 0.0996 |
| cosine_recall@1 | 0.0807 | 0.565 | 0.0125 | 0.952 |
| cosine_recall@3 | 0.1947 | 0.67 | 0.0309 | 0.9805 |
| cosine_recall@5 | 0.2627 | 0.715 | 0.0474 | 0.989 |
| cosine_recall@10 | 0.3617 | 0.79 | 0.1022 | 0.9955 |
| **cosine_ndcg@10** | **0.3456** | **0.6831** | **0.245** | **0.9743** |
| cosine_mrr@10 | 0.5344 | 0.6557 | 0.3606 | 0.9674 |
| cosine_map@100 | 0.2648 | 0.6497 | 0.0919 | 0.9676 |
#### Nano BEIR
* Dataset: `NanoBEIR_mean`
* Evaluated with [NanoBEIREvaluator](https://sbert.net/docs/package_reference/sentence_transformer/evaluation.html#sentence_transformers.sentence_transformer.evaluation.NanoBEIREvaluator) with these parameters:
```json
{
"dataset_names": [
"scidocs",
"scifact",
"nfcorpus"
],
"dataset_id": "sentence-transformers/NanoBEIR-en"
}
```
| Metric | Value |
|:--------------------|:-----------|
| cosine_accuracy@1 | 0.4267 |
| cosine_accuracy@3 | 0.5533 |
| cosine_accuracy@5 | 0.6333 |
| cosine_accuracy@10 | 0.7333 |
| cosine_precision@1 | 0.4267 |
| cosine_precision@3 | 0.2711 |
| cosine_precision@5 | 0.2213 |
| cosine_precision@10 | 0.1627 |
| cosine_recall@1 | 0.2194 |
| cosine_recall@3 | 0.2985 |
| cosine_recall@5 | 0.3417 |
| cosine_recall@10 | 0.4179 |
| **cosine_ndcg@10** | **0.4246** |
| cosine_mrr@10 | 0.5169 |
| cosine_map@100 | 0.3354 |
## Training Details
### Training Dataset
#### parquet
* Dataset: parquet
* Size: 70,764 training samples
* Columns: anchor and positive
* Approximate statistics based on the first 100 samples:
| | anchor | positive |
|:---------|:----------------------------------------------------------------------------------|:-------------------------------------------------------------------------------------|
| type | string | string |
| modality | text | text |
| details |
Los-mamba: A low-rank recursive mamba framework for mitigating stationary bias in trajectory prediction | Trajectory prediction plays a key role in autonomous driving and intelligent transportation systems. Mamba performs well in modeling long sequences but struggles with short-term static or local motion features. In this paper, we propose the Lo w-rank Recur s ive Mamba framework ( Los-Mamba ). It addresses prediction bias caused by inadequate modeling of local static features in trajectory prediction tasks. Firstly, Los-Mamba uses hybrid Mamba branches to capture both global motion trends and local features. Secondly, it reduces trajectory feature dimensionality through low-rank approximation, simplifying computational complexity. Thirdly, Los-Mamba also includes a spatio-temporal constraint mechanism. It uses position coding and a multilayer perceptron (MLP) to interpolate static and dynamic trajectories, improving the representation of local features. Experiments show that Los-Mamba outperforms baseline models on datasets like ETH and Hotel. Its average displacement error (ADE) and fi... |
| The Universal Language of CSI:Unifying Wireless Sensing Across Devices and Environments | WiFi sensing based on Channel State Information (CSI) promises ubiquitous, device-free perception, yet current research remains trapped in a Tower of Babel - fragmented into isolated silos where models are tailored to specific hardware dialects, fixed environments, and narrow tasks. The primary bottleneck is the Heterogeneity Gap: the disparity in signal dimensions, sampling rates, and semantic labels that prevents cross-system understanding. To bridge this gap, we propose a foundation-model framework that treats CSI not merely as raw signals but as a structured language with a learnable universal grammar. We first curate and standardize a large collection of heterogeneous real-world CSI datasets, establishing a unified infrastructure that allows incompatible signal formats to be treated as a single corpus. Second, we introduce a modular architecture that acts as a universal translator where lightweight dataset-specific adapters tokenize diverse signal inputs into a shared latent vocab... |
| Long-term follow-up of the transplant-eligible cohort of the EMN12/HOVON-129 study for primary plasma cell leukemia patients | Primary plasma cell leukemia (pPCL) is a rare and aggressive plasma cell disorder [ 1 , 2 ]. Compared to multiple myeloma (MM), pPCL is characterized by a higher frequency of poor-risk features, such as high-risk cytogenetic abnormalities (HRCAs) and elevated LDH [ 1 , 2 ]. Although MM treatment has improved, the survival of pPCL patients remains poor [ 1 , 2 ]. We therefore initiated the phase 2 EMN12/HOVON-129 study for patients with newly diagnosed pPCL, which showed that carfilzomib and lenalidomide-based therapy in conjunction with autologous stem-cell-transplantation (ASCT) provides efficient disease control [ 3 ]. Here, we present the long-term follow-up of patients aged 18–65 years included in the EMN12/HOVON-129 study. We also aimed to evaluate if patients with HRCAs, elevated LDH, or other high-risk features have a worse clinical outcome. Inclusion criteria were newly diagnosed pPCL (defined as >2 × 10 9 /L circulating plasma cells or >20% plasma cells in peripheral blood) an... |
* Loss: [MultipleNegativesRankingLoss](https://sbert.net/docs/package_reference/sentence_transformer/losses.html#multiplenegativesrankingloss) with these parameters:
```json
{
"scale": 20.0,
"similarity_fct": "cos_sim",
"gather_across_devices": false,
"directions": [
"query_to_doc"
],
"partition_mode": "joint",
"hardness_mode": null,
"hardness_strength": 0.0
}
```
### Evaluation Dataset
#### parquet
* Dataset: parquet
* Size: 2,000 evaluation samples
* Columns: anchor and positive
* Approximate statistics based on the first 100 samples:
| | anchor | positive |
|:---------|:----------------------------------------------------------------------------------|:-------------------------------------------------------------------------------------|
| type | string | string |
| modality | text | text |
| details | Boolean Algebra -- Driven Sepsis Diagnosis | Sepsis remains a diagnostic challenge due to its heterogeneous molecular signatures and complex immune responses. In this study, we develop a logical data analysis framework based on Boolean polynomial rings. This method constructs an ideal $\mathcal{I}$ of selection criteria that isolate empty subsets of previously analyzed patient data. This approach enables the derivation of interpretable classification rules based on biomarker profiles. We demonstrate that logical data analysis identifies distinct logical patterns for positive and negative sepsis classification. For instance, elevated levels of GLP-1 and MyD88 are associated with septic states in our dataset, whereas high TRAIL and low MyD88 concentrations may suggest a non-septic condition. Importantly, a new way to integrate expert knowledge to filter out potential overfitting or dataset-specific artifacts is shown. Our findings highlight the utility of logics in generating transparent, biologically plausible rules for a data-bas... |
| Notes on the bootstrap of four-point conformal integrals | We set up a bootstrap workflow to study four-point conformal integrals in position space, using leading singularities, single-valued multiple polylogarithmic ans\"atze and boundary data from expansion by regions. These four-point conformal integrals are general in the sense that they are generated by the four-point projections of all possible $f$-graphs, including all non-planar $f$-graph sectors. For three-loop cases, fourteen of the fifteen inequivalent integrand basis can be directly calculated by \texttt{HyperlogProcedures} and the last one is fixed by Gram identity. Then we concentrate on how far the bootstrap workflow can go for four-loop cases, though it works for three-loop cases as well. We show that integrals with several leading singularities can be made tractable by decomposing them into pieces with simpler cut structure. Some four-loop integrals which can not be calculated or very hard to be calculated by other methods for now are obtained in this way. We also provide a pa... |
| Clean2FX: Label-conditioned modeling for clean-to-effect guitar audio transformations | We present Clean2FX, a study and demo of label-conditioned clean-to-effect transformation for electric guitar audio. Given a clean guitar input and a target effect label, the task is to synthesize the corresponding effected signal while preserving the musical content. Training and evaluation pairs are constructed from EGFxSet real, single tone recordings by assembling matched clean/effected chords, melodies, and mixed timelines. This allows for controlled comparison across effects. We evaluate four neural approaches under a common spectrogram-based transformation setting: two variational autoencoders and two U-Net models that differ in whether they operate on linear or log-magnitude representations. Performance is measured using linear-magnitude spectrogram MSE and Fr\'echet Audio Distance. The U-Net models outperform the variational autoencoder variants. Per-effect results show that distortion effects are most readily improved, whereas delay and reverb effects exhibit weaker FAD gains... |
* Loss: [MultipleNegativesRankingLoss](https://sbert.net/docs/package_reference/sentence_transformer/losses.html#multiplenegativesrankingloss) with these parameters:
```json
{
"scale": 20.0,
"similarity_fct": "cos_sim",
"gather_across_devices": false,
"directions": [
"query_to_doc"
],
"partition_mode": "joint",
"hardness_mode": null,
"hardness_strength": 0.0
}
```
### Training Hyperparameters
#### Non-Default Hyperparameters
- `per_device_train_batch_size`: 16
- `learning_rate`: 2e-05
- `warmup_steps`: 0.1
- `weight_decay`: 0.01
- `fp16`: True
- `per_device_eval_batch_size`: 16
- `load_best_model_at_end`: True
- `seed`: 12
- `batch_sampler`: no_duplicates
#### All Hyperparameters