training set cohort
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| training set | associated_with | cocaine | — | 1 |
Mentioned in (28)
Papers in which this entity is mentioned.
- Accurate predictions on small data with a tabular foundation model. (2025)
- Annotating the genome at single-nucleotide resolution with DNA foundation models. (2025)
- DrBioRight 2.0: an LLM-powered bioinformatics chatbot for large-scale cancer functional proteomics analysis. (2025)
- ConsensuSV-ONT - A modern method for accurate structural variant calling. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Deep-learning-based gene perturbation effect prediction does not yet outperform simple linear baselines. (2025)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
- Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
- Predicting tumour content of liquid biopsies from cell-free DNA. (2023)
- Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
- Med-BERT: pretrained contextualized embeddings on large-scale structured electronic health records for disease prediction. (2021)
- Evaluating the transcriptional fidelity of cancer models. (2021)
- Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
- Tutorial: a guide to performing polygenic risk score analyses. (2020)
- Pan-cancer landscape of homologous recombination deficiency. (2020)
- Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
- A multi-task convolutional deep neural network for variant calling in single molecule sequencing. (2019)
- Germline variants associated with leukocyte genes predict tumor recurrence in breast cancer patients. (2019)
- The Immune Landscape of Cancer. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- GAVIN: Gene-Aware Variant INterpretation for medical sequencing. (2017)
- Copy-number signatures and mutational processes in ovarian carcinoma (2017)
- Automated cerebellar segmentation: Validation and application to detect smaller volumes in children prenatally exposed to alcohol. (2014)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)
- Facial Image Classification of Mouse Embryos for the Animal Model Study of Fetal Alcohol Syndrome. (2009)
Merged raw entities (2)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| training set | cohort | 36 | 61 |
| training sample | cohort | 5 | 12 |