arXiv subjects

Bharath Dandala

Publications and source records attributed to Bharath Dandala.

6 recordsLinked to original sources

arXiv2026

RLMOpt: Adaptive Prompt Optimization via Recursive Language Models

Prompt optimizers automate the search for prompts that improve language-model performance, but existing methods rely on a predefined optimization procedure: the algorithm determines which candidates to explore and how the search progresses, while the language model generates or refines prompt proposals. We introduce RLMOpt, a prompt optimizer that makes the search policy itself language-model-driven through a recursive language model (RLM). The RLM agent operates over a tool-based environment, inspecting task information, analyzing failures, generating candidates, allocating evaluation budget, and deciding when to stop. A deterministic harness complements the agent by enforcing objective scoring, Pareto-based selection, and regression constraints. We evaluate RLMOpt across four benchmarks spanning structured clinical information extraction (Chia), multi-hop question answering (HotpotQA), verifiable instruction following (IFBench-2025), and multi-turn tool-calling agents (BFCL). In a matched comparison at a single seed, RLMOpt obtains the best held-out score on all four benchmarks and leads the four-task mean (0.610 against 0.589 for GEPA). Repeating each benchmark across seeds yields 11 matched benchmark-seed comparisons, in which RLMOpt outperforms GEPA in 9 cases. Across all 11 runs, it never produced a prompt that underperformed its seed, whereas GEPA fell below its starting point twice. It is also more efficient, achieving these results with fewer search rollouts while producing prompts that are 27-79% the size of those produced by GEPA. Our results further show that optimization gains are determined primarily by the headroom available in the seed prompt, rather than by the search budget. Efficient optimization therefore depends on reaching the available headroom reliably and with minimal search

cs.AI↗

arXiv2026

BMFM-RNA: whole-cell expression decoding improves transcriptomic foundation models

Transcriptomic foundation models pretrained with masked language modeling can achieve low pretraining loss yet produce poor cell representations for downstream tasks. We introduce whole-cell expression decoding (WCED), where models reconstruct the entire gene vocabulary from a single CLS token embedding, even with limited inputs, creating a maximally informative bottleneck. WCED consistently outperforms MLM on all downstream metrics despite higher reconstruction error during training. Gene-level error tracking reveals that both methods preferentially learn genes whose expression co-varies with stable transcriptional programs rather than those driven by transient factors. We further add hierarchical cross-entropy loss that exploits Cell Ontology structure for zero-shot annotation at multiple granularity levels. Models trained with these objectives achieve best overall performance across CZI benchmarks, on zero-shot batch integration and linear probing cell-type annotation. Methods are implemented in biomed-multi-omic ( https://github.com/BiomedSciAI/biomed-multi-omic ), an open-source framework for transcriptomic foundation model development.

q-bio.GN↗

arXiv2025

BMFM-DNA: A SNP-aware DNA foundation model to capture variant effects

Large language models (LLMs) trained on text demonstrated remarkable results on natural language processing (NLP) tasks. These models have been adapted to decipher the language of DNA, where sequences of nucleotides act as "words" that encode genomic functions. However, the genome differs fundamentally from natural language, as it lacks clearly defined words or a consistent grammar. Although DNA language models (DNALMs) such as DNABERT, GENA-LM have achieved high level of performance on genome-related biological tasks, these models do not encode biological functions in the presence of sequence variations. To address this problem, we pre-train foundation models that effectively integrate sequence variations, in particular Single Nucleotide Polymorphisms (SNPs), as they underlie important biological functions. Specifically, we use ModernBERT to pre-train two different Biomedical Foundation Models (BMFM), namely, BMFM-DNA-REF in which the model is trained with sequences of varying lengths along with their reverse complements derived from the reference genome and BMFM-DNA-SNP in which the model is trained with sequences created using a novel representation scheme that encodes sequence variations. Our findings indicate that integrating sequence variations into DNALMs helps capture the biological functions as seen in improvements on all fine-tuning tasks. To explore the model's practical utility, we experimented with various strategies for SNP imputation on promoter detection task introduced in DNABERT-2. However, we acknowledge that the current benchmarks are limited in their ability to fully evaluate these models. To enable more comprehensive assessment in the future and encourage community contributions, we release our models through HuggingFace and the code to reproduce the results at https://github.com/BiomedSciAI/biomed-multi-omic

q-bio.GN↗

arXiv2024

INDUS: Effective and Efficient Language Models for Scientific Applications

Large language models (LLMs) trained on general domain corpora showed remarkable results on natural language processing (NLP) tasks. However, previous research demonstrated LLMs trained using domain-focused corpora perform better on specialized tasks. Inspired by this insight, we developed INDUS, a comprehensive suite of LLMs tailored for the closely-related domains of Earth science, biology, physics, heliophysics, planetary sciences and astrophysics, and trained using curated scientific corpora drawn from diverse data sources. The suite of models include: (1) an encoder model trained using domain-specific vocabulary and corpora to address NLP tasks, (2) a contrastive-learning based text embedding model trained using a diverse set of datasets to address information retrieval tasks and (3) smaller versions of these models created using knowledge distillation for applications which have latency or resource constraints. We also created three new scientific benchmark datasets, CLIMATE-CHANGE NER (entity-recognition), NASA-QA (extractive QA) and NASA-IR (IR) to accelerate research in these multi-disciplinary fields. We show that our models outperform both general-purpose (RoBERTa) and domain-specific (SCIBERT) encoders on these new tasks as well as existing tasks in the domains of interest. Furthermore, we demonstrate the use of these models in two industrial settings -- as a retrieval model for large-scale vector search applications and in automatic content tagging systems.

cs.CL↗

arXiv2021

WNTRAC: AI Assisted Tracking of Non-pharmaceutical Interventions Implemented Worldwide for COVID-19

The Coronavirus disease 2019 (COVID-19) global pandemic has transformed almost every facet of human society throughout the world. Against an emerging, highly transmissible disease with no definitive treatment or vaccine, governments worldwide have implemented non-pharmaceutical intervention (NPI) to slow the spread of the virus. Examples of such interventions include community actions (e.g. school closures, restrictions on mass gatherings), individual actions (e.g. mask wearing, self-quarantine), and environmental actions (e.g. public facility cleaning). We present the Worldwide Non-pharmaceutical Interventions Tracker for COVID-19 (WNTRAC), a comprehensive dataset consisting of over 6,000 NPIs implemented worldwide since the start of the pandemic. WNTRAC covers NPIs implemented across 261 countries and territories, and classifies NPI measures into a taxonomy of sixteen NPI types. NPI measures are automatically extracted daily from Wikipedia articles using natural language processing techniques and manually validated to ensure accuracy and veracity. We hope that the dataset is valuable for policymakers, public health leaders, and researchers in modeling and analysis efforts for controlling the spread of COVID-19.

cs.CY↗

arXiv2019

Training Models to Extract Treatment Plans from Clinical Notes Using Contents of Sections with Headings

Objective: Using natural language processing (NLP) to find sentences that state treatment plans in a clinical note, would automate plan extraction and would further enable their use in tools that help providers and care managers. However, as in the most NLP tasks on clinical text, creating gold standard to train and test NLP models is tedious and expensive. Fortuitously, sometimes but not always clinical notes contain sections with a heading that identifies the section as a plan. Leveraging contents of such labeled sections as a noisy training data, we assessed accuracy of NLP models trained with the data. Methods: We used common variations of plan headings and rule-based heuristics to find plan sections with headings in clinical notes, and we extracted sentences from them and formed a noisy training data of plan sentences. We trained Support Vector Machine (SVM) and Convolutional Neural Network (CNN) models with the data. We measured accuracy of the trained models on the noisy dataset using ten-fold cross validation and separately on a set-aside manually annotated dataset. Results: About 13% of 117,730 clinical notes contained treatment plans sections with recognizable headings in the 1001 longitudinal patient records that were obtained from Cleveland Clinic under an IRB approval. We were able to extract and create a noisy training data of 13,492 plan sentences from the clinical notes. CNN achieved best F measures, 0.91 and 0.97 in the cross-validation and set-aside evaluation experiments respectively. SVM slightly underperformed with F measures of 0.89 and 0.96 in the same experiments. Conclusion: Our study showed that the training supervised learning models using noisy plan sentences was effective in identifying them in all clinical notes. More broadly, sections with informal headings in clinical notes can be a good source for generating effective training data.

cs.CL↗