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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TriticeaeExpDB: a centralized transcriptomic resource for Triticeae research.
PMID 41656232 · PMC12983667 · BMC genomics · 2026 · 8 claims · 8 setups
TriticeaeExpDB integrates and uniformly reprocesses >10,000 (11,016) RNA-seq samples from 528 BioProjects/studies across 17 Triticeae species
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Has reproduction · 71
Comprehensive comparison of gene expression diversity among a variety of human stem cells.
PMID 36458020 · PMC9706419 · NAR genomics and bioinformatics · 2022 · 8 claims · 8 setups
Tissue origin has a stronger influence on gene expression in iPSCs than in other stem cell types
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Alternative splicing in pediatric central nervous system tumors highlights oncofetal candidate CLK1 exon 4.
PMID 41908886 · PMC13017157 · Neuro-oncology pediatrics · 2026 · 8 claims · 6 setups
Alternative splicing defines biologically and prognostically meaningful tumor subgroups in pediatric CNS tumors beyond traditional histologic classification
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Transcriptomics Reveal Molecular Signatures of a Resolved Sexual Conflict and Potential Association With Colour Polymorphism in Tawny Owls.
PMID 41964128 · PMC13069001 · Molecular ecology · 2026 · 8 claims · 8 setups
Substantial sex-specific variation exists in differentially expressed genes, SNPs and alternative exon usage in genes involved in life history traits (ZGRF1, VLDLR), behaviour (GSK3B, SLC12A) and growth (GHR, EGF, EPS8L2)
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Has reproduction · 50
Polymorphism identification and improved genome annotation of Brassica rapa through Deep RNA sequencing.
PMID 25122667 · PMC4232532 · G3 (Bethesda, Md.) · 2014 · 8 claims · 8 setups
330,995 SNPs were identified in transcribed regions between B. rapa genotypes R500 and IMB211, at an average frequency of one SNP per 200 bases.
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Lineage-Specific Disruption of Hematopoiesis by Oxaliplatin: Mechanisms of Erythropoietin Resistance and Immune Suppression.
PMID 41868970 · PMC13005433 · Journal of hematology and oncology research · 2026 · 8 claims · 5 setups
Oxaliplatin induces coordinated, lineage-dependent suppression of hematopoiesis, strongest in erythroid and lymphoid lineages while neutrophils are relatively spared
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Has reproduction · 50
Quality control method for RNA-seq using single nucleotide polymorphism allele frequency.
PMID 25243705 · PMC4231238 · Genes to cells : devoted to molecular & cellular mechanisms · 2014 · 8 claims · 8 setups
SNP allele frequency distributions from RNA-seq reads can detect contaminating cells whose genomic background differs from the target cells; the mode of the distribution reflects the cellular composition while its variance reflects PCR bias.
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Has reproduction · 54
Mining transcriptomic data to study the origins and evolution of a plant allopolyploid complex.
PMID 24883252 · PMC4034613 · PeerJ · 2014 · 8 claims · 8 setups
All three allopolyploid species are fixed hybrids combining the genomes of the two putative diploid parents hypothesized on the basis of previous crossing and molecular work.
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Has reproduction · 78
Evaluating Distribution and Prognostic Value of New Tumor-Infiltrating Lymphocytes in HCC Based on a scRNA-Seq Study With CIBERSORTx.
PMID 33043022 · PMC7527443 · Frontiers in medicine · 2020 · 6 claims · 8 setups
CIBERSORTx can combine scRNA-seq-derived signature matrices with bulk RNA-seq data to estimate proportions of 11 TIL subsets in HCC tumor and normal tissue
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Development of a pediatric immune cell atlas and characterization of CD4+ T cells in food allergy.
PMID 42025535 · PMC13105851 · Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026 · 8 claims · 8 setups
A pediatric single-cell PBMC reference atlas was developed from 57 healthy children across 8 public scRNA-seq studies.
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isoSeQL: comparing long-read isoforms across multiple datasets.
PMID 41452740 · PMC12790818 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 4 setups
isoSeQL enables comparison of long-read isoform profiles across multiple datasets by consolidating SQANTI3-annotated samples into a unified SQLite database with consistent isoform IDs