autoimmune diseases phenotype

Aliases

autoimmune disease

Related entities (1)

Mentioned in (34)

Papers in which this entity is mentioned.

• Artificial Intelligence agents for biological research: a survey. (2026)
• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• The Human Phenotype Ontology in 2024: phenotypes around the world. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• My Health Coach: Community members' perspectives on a mobile health tool for adults with fetal alcohol spectrum disorders. (2024)
• Alcohol and Immunology: Mechanisms of multi-organ damage. Summary of the 2022 alcohol and Immunology research interest group (AIRIG) meeting. (2023)
• Towards understandings of serine/arginine-rich splicing factors. (2023)
• At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
• Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
• Macrophage Polarization States in the Tumor Microenvironment. (2021)
• Pan-cancer analysis of longitudinal metastatic tumors reveals genomic alterations and immune landscape dynamics associated with pembrolizumab sensitivity. (2021)
• MHCAttnNet: predicting MHC-peptide bindings for MHC alleles classes I and II using an attention-based deep neural model. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• HLA-VBSeq v2: improved HLA calling accuracy with full-length Japanese class-I panel. (2019)
• Rare variant phasing using paired tumor:normal sequence data. (2019)
• HLA*LA-HLA typing from linearly projected graph alignments. (2019)
• The Human Transcription Factors. (2018)
• Fast and accurate HLA typing from short-read next-generation sequence data with xHLA. (2017)
• Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin. (2016)
• B lymphocytes and cancer: a love-hate relationship. (2016)
• High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• What Happens When Children with Fetal Alcohol Spectrum Disorders Become Adults? (2015)
• Experiences with workflows for automating data-intensive bioinformatics. (2015)
• HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• OptiType: precision HLA typing from next-generation sequencing data. (2014)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
• Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (2010)
• The HLA system: genetics, immunology, clinical testing, and clinical implications. (2007)

Merged raw entities (4)

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