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Fiona Hak

dblp:436/4719 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2026
0009-0002-8296-1747ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 81% Medical and health informatics · 19%

Topics — the 2 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › transcriptomics
cancer transcriptomics
0.312026
Metappuccino: large language model-driven reconstruction of sequence read archive metadata for cancer research · Bioinform. 2026
Medical and health informatics › biomedical data science
cohort discovery
0.312026
Metappuccino: large language model-driven reconstruction of sequence read archive metadata for cancer research · Bioinform. 2026

Methods — techniques the papers use, named apart from their topics

rule-based extraction · 1.0ontology mapping · 1.0low-rank adaptation · 1.0large language model · 1.0
YearPublicationVenuePosition
2026 Metappuccino: large language model-driven reconstruction of sequence read archive metadata for cancer research
abstract
MOTIVATION: High-throughput RNA sequencing has significantly advanced transcriptomic profiling in oncology. Millions of RNA-seq datasets have accumulated in public databases such as the Sequence Read Archive (SRA). However, fragmented, ambiguous, or missing metadata can severely limit accurate cohort selection, introduce bias, and delay discoveries. RESULTS: To address these issues, we introduce 'Metappuccino', a hybrid metadata enrichment tool built on Mistral-7B-Instruct and specialized via low-rank adaptation (LoRA). Metappuccino reconstructs 19 metadata classes (e.g. organ, disease, cell type) by combining deterministic extraction/normalization with model-based completion: 4 submission-mandatory fields are read directly from SRA/API records, while the remaining 15 classes are obtained through validated rule-based extraction when explicitly supported by the context and otherwise predicted by the LoRA-specialized model when information is missing or ambiguous. To promote robust, context-aware inference rather than memorization, we designed training and data partitioning to minimize leakage and preserve generalization. When applicable, predicted values are mapped to standardized ontologies to ensure consistent, interoperable annotations. Across our benchmarks, Metappuccino substantially improves accuracy over the base model, matches or exceeds recent larger open-source LLMs, and reduces inference time by up to two-fold relative to these baselines. By enriching under-annotated public RNA-seq records, Metappuccino increases the usability of SRA datasets for large-scale reuse, with applications that extend beyond oncology transcriptomics. AVAILABILITY AND IMPLEMENTATION: Metappuccino source code is available on: github.com/chumphati/Metappuccino. The fine-tuned LLM, MetappuccinoLLModel, is available on: huggingface.co/chumphati/MetappuccinoLLModel. Both repositories are released under Apache-2.0 license.
Fiona Hak, Camille Marchet, Daniel Gautheret, Mélina Gallopin
Bioinform.1