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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Dissecting tumor heterogeneity in colorectal cancer: uncovering the role of BCL2L1(+) cells through single-cell analysis.
PMID 41958675 · PMC13056825 · Frontiers in immunology · 2026 · 8 claims · 8 setups
scRNA-seq identifies five CRC tumor cell subtypes, with the C4 BCL2L1+ subtype predominantly enriched in liver metastases and showing enhanced proliferation, metabolic reprogramming, and anti-apoptotic activity
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Has reproduction · 67
HArmonized single-cell RNA-seq Cell type Assisted Deconvolution (HASCAD).
PMID 37907883 · PMC10619225 · BMC medical genomics · 2023 · 6 claims · 4 setups
Removal of batch effects in reference scRNA-seq datasets (via Harmony-Symphony) benefits the task of cell composition deconvolution
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Statistical challenges in preprocessing in microarray experiments in cancer.
PMID 18829474 · PMC3529914 · Clinical cancer research : an official journal of the American Association for Cancer Research · 2008 · 8 claims · 7 setups
Choice of pre-processing method materially changes which features are found significantly associated with survival in the Beer et al. lung cancer microarray dataset
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TE-SCALE: a comprehensive database for exploring transposable element expression across human cancers at single-cell resolution.
PMID 41296555 · PMC12807651 · Nucleic acids research · 2026 · 8 claims · 8 setups
TE-SCALE is a comprehensive single-cell database integrating TE expression across 20 human cancer types and 12 tissue origins
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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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Has reproduction · 10
RADAR: differential analysis of MeRIP-seq data with a random effect model.
PMID 31870409 · PMC6927177 · Genome biology · 2019 · 8 claims · 6 setups
RADAR is a novel analytical tool for differential methylation analysis of MeRIP-seq data combining gene-level INPUT normalization with a Poisson random effect model.
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FAP expression as a marker of malignant transformation enabling in vivo characterization in peripheral nerve sheath tumors: a multimodal and translational study.
PMID 41591566 · PMC12847211 · Acta neuropathologica · 2026 · 8 claims · 7 setups
FAP is consistently upregulated in MPNSTs compared to neurofibromas at the transcript level across independent bulk datasets
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Ion-Channel-Mediated Drug Repurposing Opportunities Validated by Single-Cell Perturbation in Colorectal Cancer.
PMID 42074061 · PMC13116841 · International journal of molecular sciences · 2026 · 8 claims · 6 setups
WGCNA on CRC transcriptomes identified 100 hub genes spanning three functional programs: ribosomal biogenesis, RNA processing, and immune
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Has reproduction · 67
Generative and integrative modeling for transcriptomics with formalin fixed paraffin embedded material.
PMID 41029822 · PMC12486589 · Journal of translational medicine · 2025 · 8 claims · 6 setups
The negative binomial distribution best fits fRNA-seq transcript counts, with little evidence supporting zero-inflated extensions
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Resolving sensitivity, specificity and signal contamination in Xenium spatial transcriptomics.
PMID 42062553 · PMC13259927 · Nature methods · 2026 · 8 claims · 6 setups
Xenium data show strong consistency across patients and technical replicates, with little technical variation between platforms
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Genomics, molecular imaging, bioinformatics, and bio-nano-info integration are synergistic components of translational medicine and personalized healthcare research.
PMID 18831773 · PMC3226104 · BMC genomics · 2008 · 8 claims · 8 setups
Genomics, molecular imaging, bioinformatics, and bio-nano-info integration are synergistic components of translational medicine and personalized healthcare