Genetics

Discover the top 1% of genetics preprints on bioRxiv, ranked by QED Score for originality and validity. Browse new research on heredity, genetic variation, GWAS, population genetics, gene function, and the genetic basis of disease, and see the claims and evidence behind each paper at a glance.

15

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How the QED Score works

QED Score is a validated AI-based quality metric that evaluates life science papers on two dimensions: originality and validity. Each manuscript is anonymized, broken down into its claims and supporting evidence, and examined by specialized AI agents for statistical rigor, consistency across figures, and fit with the existing literature. Scores are percentile ranks, so they're comparable across fields. In blinded tests, expert professors sided with QED Score over journal rank in 75% of decisive cases.

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Physiology

Animal Behavior and Cognition

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Developmental Biology

Genetics

Xist Repeat A coordinates an assembly of SR proteins to recruit SPEN and induce gene silencing

Single-cell eQTL mapping reveals convergent glial–neuronal risk architecture in Parkinson’s disease

Intercellular communication is a heritable dimension of human tissue architecture

Genetic variation reveals a homeotic long noncoding RNA that modulates human hematopoietic stem cells

Decoding Chromatin Dynamics in Cardiac Organoids Reveals Genetic Drivers of Human Heart Development and Disease

Primate lineage specification requires suppression of Alu hyperediting

Genome-scale mapping of variant, enhancer and gene function in primary human CD4+ T cells

A Vertebrate Toxin-Antidote System That Sabotages Mouse Embryogenesis

The craniofacial shape of modern humans embodies genomic signatures of evolution, diversity, and clinical conditions

Genome-scale perturb-seq in primary human CD4+ T cells maps context-specific regulators of T cell programs and human immune traits

A shared DNA-repeat toxicity threshold, reached somatically at cell-type-specific rates, unites cortical and striatal neurodegeneration in Huntington’s disease

A unified genetic perturbation language for human cellular programming

Antisense transposon insertions into host genes trigger piRNA mediated immunity

Non-disruptive 3D profiling of combinations of epigenetic marks in single cells

Lysosomes Signal through Epigenome to Regulate Longevity across Generations

Lysosomes Signal through Epigenome to Regulate Longevity across Generations

Non-disruptive 3D profiling of combinations of epigenetic marks in single cells

Antisense transposon insertions into host genes trigger piRNA mediated immunity

A unified genetic perturbation language for human cellular programming

A shared DNA-repeat toxicity threshold, reached somatically at cell-type-specific rates, unites cortical and striatal neurodegeneration in Huntington’s disease

Genome-scale perturb-seq in primary human CD4+ T cells maps context-specific regulators of T cell programs and human immune traits

The craniofacial shape of modern humans embodies genomic signatures of evolution, diversity, and clinical conditions

A Vertebrate Toxin-Antidote System That Sabotages Mouse Embryogenesis

Genome-scale mapping of variant, enhancer and gene function in primary human CD4+ T cells

Primate lineage specification requires suppression of Alu hyperediting

Decoding Chromatin Dynamics in Cardiac Organoids Reveals Genetic Drivers of Human Heart Development and Disease

Genetic variation reveals a homeotic long noncoding RNA that modulates human hematopoietic stem cells

Intercellular communication is a heritable dimension of human tissue architecture

Single-cell eQTL mapping reveals convergent glial–neuronal risk architecture in Parkinson’s disease

Xist Repeat A coordinates an assembly of SR proteins to recruit SPEN and induce gene silencing

Antisense transposon insertions into host genes trigger piRNA mediated immunity

A shared DNA-repeat toxicity threshold, reached somatically at cell-type-specific rates, unites cortical and striatal neurodegeneration in Huntington’s disease

A unified genetic perturbation language for human cellular programming

A Vertebrate Toxin-Antidote System That Sabotages Mouse Embryogenesis

Decoding Chromatin Dynamics in Cardiac Organoids Reveals Genetic Drivers of Human Heart Development and Disease

Genetic variation reveals a homeotic long noncoding RNA that modulates human hematopoietic stem cells

Genome-scale mapping of variant, enhancer and gene function in primary human CD4+ T cells

Genome-scale perturb-seq in primary human CD4+ T cells maps context-specific regulators of T cell programs and human immune traits

Intercellular communication is a heritable dimension of human tissue architecture

Lysosomes Signal through Epigenome to Regulate Longevity across Generations

Non-disruptive 3D profiling of combinations of epigenetic marks in single cells

Primate lineage specification requires suppression of Alu hyperediting

Single-cell eQTL mapping reveals convergent glial–neuronal risk architecture in Parkinson’s disease

The craniofacial shape of modern humans embodies genomic signatures of evolution, diversity, and clinical conditions

Xist Repeat A coordinates an assembly of SR proteins to recruit SPEN and induce gene silencing

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