Experiments
Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).
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Interpretable, flexible and spatially aware integration of multiple spatial transcriptomics datasets from diverse sources.
PMID 42045691 · PMC13175893 · Nature genetics · 2026 · 6 claims · 7 setups
INSPIRE is a deep-learning method that unifies adversarial learning with a GNN-based encoder and integrated NMF to interpretably integrate multiple spatial transcriptomics datasets
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Charting spatial ligand-target activity using Renoir.
PMID 42086556 · PMC13144314 · Nature communications · 2026 · 8 claims · 8 setups
Renoir computes a neighborhood activity score for curated ligand-target pairs at each spatial spot/cell by integrating cell type abundance, cell type-specific mRNA abundance, receptor expression, gene entropy, and mutual information between ligand and target genes.
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Integrating single-cell and single-nucleus datasets improves bulk RNA-seq deconvolution.
PMID 41895263 · PMC13106970 · Cell reports methods · 2026 · 8 claims · 5 setups
scRNA-seq references yield significantly higher Pearson correlation and lower RMSE than snRNA-seq references for deconvolution across all four tissue datasets
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Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach.
PMID 17010196 · PMC1592491 · BMC genomics · 2006 · 8 claims · 7 setups
High-throughput 454 sequencing-by-synthesis of LNCaP cDNA can profile transcript abundance across the transcriptome
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Has reproduction · 37
A Bayesian approach to accurate and robust signature detection on LINCS L1000 data.
PMID 32003771 · PMC7203754 · Bioinformatics (Oxford, England) · 2020 · 7 claims · 4 setups
A novel Bayesian peak deconvolution algorithm gives unbiased likelihood estimations for peak locations and derives probability-based z-scores.
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scGeno: a Hidden Markov Model approach to denoise chromosome-scale genotypes from single-cell data.
PMID 41982479 · PMC13075984 · Bioinformatics advances · 2026 · 7 claims · 4 setups
scGeno, a categorical HMM, infers chromosome-level genotype states in mixed-genotype organisms by modeling sequential single-cell allelic expression ratios along chromosomes