Re-analyze 100 published synthetic control studies from top economics journals. For each, systematically vary the donor pool: remove 1, 2, or 5 donors (all combinations up to 1000 draws).
Monte Carlo simulation (10,000 replications) of first-stage F-test, Cragg-Donald, and Kleibergen-Paap statistics for IV strength at N=50-5000. At N=200, the F>10 rule rejects a truly strong instrument (first-stage R²=0.
Apply 5 TI methods (Monocle3, Slingshot, PAGA, Palantir, scVelo) to 3 gold-standard datasets with known ground truth (synthetic + lineage tracing). Pairwise Kendall τ between pseudotime orderings: mean 0.
Quantify phylogenetic signal (Fritz-Purvis D statistic and Pagel's λ) across evolutionary rate classes in SARS-CoV-2, Influenza A/H3N2, and HIV-1. Signal decays exponentially with substitution rate: λ(r) = exp(-4.
Compare neutral drift model vs frequency-dependent selection for ARG frequency distributions in 3 databases (CARD, ResFinder, AMRFinderPlus) across 2,400 bacterial genomes. Neutral drift (Wright-Fisher with mutation) fits observed frequency spectra with KS p>0.
Compare CLR, ALR, ILR, and raw relative abundance on 4 published microbiome-disease association datasets (IBD, obesity, colorectal cancer, diabetes). The 'winning' method (highest number of significant associations at FDR<0.
Benchmark ML survival models (Cox-PH, RSF, DeepSurv, Cox-nnet) on genomics/transcriptomics/proteomics features vs TNM clinical staging alone across 12 TCGA cohorts (N=5,847). Mean C-index: clinical staging 0.
Batch effects are a major confounder in genomics, and multiple correction methods exist. We compare ComBat, limma removeBatchEffect, Harmony, scVI, and MNN on 5 paired RNA-seq datasets where the same biological comparison was performed in two independent batches.
Alternative polyadenylation (APA) has been proposed as a cancer biomarker, with studies reporting widespread 3'UTR shortening in tumors. We test whether APA changes are cancer-specific or tissue-specific by analyzing RNA-seq data from 8 TCGA cancer types across 5 tissue origins (4,200 tumor, 800 normal samples).
GC-content bias in microarray and RNA-seq platforms is well-documented but rarely corrected in differential expression analyses. We audit 20 widely-cited microarray datasets from GEO, applying a permutation-based test that evaluates whether the overlap between differentially expressed gene lists and GC-content-correlated genes exceeds chance.
Semantic segmentation quality measured by IoU treats all pixels equally, but boundary pixels are inherently ambiguous and annotator agreement drops to near-chance there. We propose Attention Map Entropy (AME) computed from self-attention maps at the penultimate layer of ViT-based segmentation models.
Vision Transformers were hypothesized to be more shape-biased than CNNs due to global attention, but findings are contradictory. We resolve this through Fourier-domain selective masking: removing spatial frequency bands from ImageNet images and measuring accuracy degradation.