Fast and efficient QTL mapper for thousands of molecular phenotypes.
- Authors
- Ongen, Halit; Buil, Alfonso; Brown, Andrew Anand; Dermitzakis, Emmanouil T; Delaneau, Olivier
- Year
- 2016
- Journal
- Bioinformatics (Oxford, England)
- PMID
- 26708335
- DOI
- 10.1093/bioinformatics/btv722
- PMCID
- PMC4866519
MOTIVATION: In order to discover quantitative trait loci, multi-dimensional genomic datasets combining DNA-seq and ChiP-/RNA-seq require methods that rapidly correlate tens of thousands of molecular phenotypes with millions of genetic variants while appropriately controlling for multiple testing. RESULTS: We have developed FastQTL, a method that implements a popular cis-QTL mapping strategy in a user- and cluster-friendly tool. FastQTL also proposes an efficient permutation procedure to control for multiple testing. The outcome of permutations is modeled using beta distributions trained from a few permutations and from which adjusted P-values can be estimated at any level of significance with little computational cost. The Geuvadis & GTEx pilot datasets can be now easily analyzed an order of magnitude faster than previous approaches. AVAILABILITY AND IMPLEMENTATION: Source code, binaries and comprehensive documentation of FastQTL are freely available to download at http://fastqtl.sourceforge.net/ CONTACT: emmanouil.dermitzakis@unige.ch or olivier.delaneau@unige.ch SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
(a, b) Density plots of the k and n parameter ML estimates made from 100, 1K, 10K and 100K permutations on GEUV_EUR. (c) A scatter plot of the number of variant sites tested per gene (cis-window Β±1Mb of the TSS) against the n parameter ML estimates made again from 100, 1K, 10K and 100K permutations on GEUV_EUR. (d, e) QuantileβQuantile plots of the best P-values obtained through 1000 permutations (observed) of the GEUV_EUR dataset against simulated P-values sampled from the fitted beta distributions (expected). Expected P-values are plotted against the observed ones for all genes pooled together in (d) and for each gene separately in panel (e). (f) The KS test βlog10 P-values comparing observations and expectations for each gene. The red line shows the expected Bonferroni significance threshold when testing 13 703 genes
(a, b) Scatter plots of the adjusted P-values obtained from 1000 permutations via the direct method (in grey) and the beta approximation (in light blue) against those obtained through the standard permutation scheme with 100K permutations (a) or through the adaptive method with up to 1M permutations (b). All this was performed on the GEUV_EUR dataset. Adjusted P-values are plotted on both linear (a) and log (b) scales. Expected variation for 1000 permutations is shown by the 95% confidence intervals in red. (c) The equivalent number of permutations required by the direct permutation scheme to reach the same calibration as the beta approximation (from 1000 permutations) as a function of the adjusted P-value targeted. The dashed and solid gray lines show the expected accuracy of the adaptive permutation scheme that stops when 5 and 10 stronger null signals are found, respectively. (d) The sensitivityβspecificity ratio of reasonable FastQTL runs (beta approximation or direct method with 50β5000 permutations) to recover an optimal eQTL set derived from 100 000 permutations. (e) The sensitivityβspecificity ratio to recover the nine official eQTL sets released by the GTEx consortium using both Matrix eQTL (direct method) and FastQTL (beta approximation) with 100, 500 and 1000 permutations
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| Citation | PMID | DOI | Status |
|---|---|---|---|
| AulchenkoY.S. (2007) GenABEL: an R library for genome-wide association analysis. Bioinformatics, 23, 1294β1296.1738401510.1093/bioinformatics/btm108 | β | β | β |
| BenjaminiY.HochbergY. (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. R. Stat. Soc., 57, 289β300. | β | β | β |
| DudbridgeF.KoelemanB.P. (2004) Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies. Am. J. Hum. Genet., 75, 424β435.1526639310.1086/423738PMC1182021 | β | β | β |
| FairfaxB.P. (2012) Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles. Nat. Genet., 44, 502β510.2244696410.1038/ng.2205PMC3437404 | β | β | β |
| FlutreT. (2013) A statistical framework for joint eQTL analysis in multiple tissues. PLoS Genet., 9, e1003486.2367142210.1371/journal.pgen.1003486PMC3649995 | β | β | β |
| FusiN. (2012) Joint modelling of confounding factors and prominent genetic regulators provides increased accuracy in genetical genomics studies. PLoS Comput. Biol., 8, e1002330.2224197410.1371/journal.pcbi.1002330PMC3252274 | β | β | β |
| GaffneyD.J. (2012) Dissecting the regulatory architecture of gene expression QTLs. Genome Biol., 13, R7 (2012 Jan 31)2229303810.1186/gb-2012-13-1-r7PMC3334587 | β | β | β |
| GalweyN.W. (2009) A new measure of the effective number of tests, a practical tool for comparing families of non-independent significance tests. Genet. Epidemiol., 33, 559β568.1921702410.1002/gepi.20408 | β | β | β |
| GTEx Consortium (2015) The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science, 348, 648β660.2595400110.1126/science.1262110PMC4547484 | β | β | β |
| HubnerN. (2005) Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease. Nat. Genet., 37, 243β253.1571154410.1038/ng1522 | β | β | β |
| JonesM.C. (2009) Kumaraswamyβs distribution: a beta-type distribution with some tractability advantages. Stat. Methodol., 6, 70β81. | β | β | β |
| LappalainenT. (2013) Transcriptome and genome sequencing uncovers functional variation in humans. Nature, 501, 506β511.2403737810.1038/nature12531PMC3918453 | β | β | β |
| LiH. (2011) Tabix: fast retrieval of sequence features from generic TAB-delimited files. Bioinformatics, 27, 718β719.2120898210.1093/bioinformatics/btq671PMC3042176 | β | β | β |
| MauranoM.T. (2012) Systematic localization of common disease-associated variation in regulatory DNA. Science, 337, 1190β1195.2295582810.1126/science.1222794PMC3771521 | β | β | β |
| MontgomeryS.B. (2010) Transcriptome genetics using second generation sequencing in a Caucasian population. Nature, 464, 773β777.2022075610.1038/nature08903PMC3836232 | β | β | β |
| NicaA.C. (2010) Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations. PLoS Genet., 6, e1000895.2036902210.1371/journal.pgen.1000895PMC2848550 | β | β | β |
| OngenH. (2014) Putative cis-regulatory drivers in colorectal cancer. Nature, 512, 87β90.2507932310.1038/nature13602 | β | β | β |
| PhipsonB.SmythG.K. (2010) Permutation P-values should never be zero: calculating exact P-values when permutations are randomly drawn. Stat. Appl. Genet. Mol. Biol., 9, Article39. doi:10.2202/1544-6115.1585.2104404310.2202/1544-6115.1585 | β | β | β |
| ShabalinA.A. (2012) Matrix eQTL: ultra fast eQTL analysis via large matrix operations. Bioinformatics, 28, 1353β1358.2249264810.1093/bioinformatics/bts163PMC3348564 | β | β | β |
| StegleO. (2012) Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses. Nat. Protoc., 7, 500β507.2234343110.1038/nprot.2011.457PMC3398141 | β | β | β |
| StoreyJ.D.TibshiraniR. (2003) Statistical significance for genomewide studies. Proc. Natl Acad. Sci., 100, 9440β9445.1288300510.1073/pnas.1530509100PMC170937 | β | β | β |
| van de GeijnB. (2015) WASP: allele-specific software for robust molecular quantitative trait locus discovery. Nat. Methods, 12, 1061β1063.2636698710.1038/nmeth.3582PMC4626402 | β | β | β |
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|---|---|---|---|---|
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| Genotype inference from aggregated chromatin accessibility data reveals genetic regulatory mechanisms. | Wenz BM et al. | β | 2025 | β |
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| Potentially causal associations between placental DNA methylation and schizophrenia and other neuropsychiatric disorders. | Cilleros-Portet A et al. | β | 2025 | β |
| Protein arginine methyltransferase 7 linked to schizophrenia through regulation of neural progenitor cell proliferation and differentiation. | Shen T et al. | β | 2025 | β |
| reg-eQTL: Integrating transcription factor effects to unveil regulatory variants. | Mudappathi R et al. | β | 2025 | β |
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| The impact of haplotypes derived from Chinese pigs on genetic variation and economic traits in the Duroc breed. | Fang S et al. | β | 2025 | β |
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| A common polymorphism in the Intelectin-1 gene influences mucus plugging in severe asthma. | Everman JL et al. | β | 2024 | β |
| A landscape of gene expression regulation for synovium in arthritis. | Jiang F et al. | β | 2024 | β |
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| Shared and distinct pathways and networks genetically linked to coronary artery disease between human and mouse. | Kurt Z et al. | β | 2023 | β |
| Single-cell genomics meets human genetics. | Cuomo ASE et al. | β | 2023 | β |
| Single-cell multiomics of the human retina reveals hierarchical transcription factor collaboration in mediating cell type-specific effects of genetic variants on gene regulation. | Wang J et al. | β | 2023 | β |
| Summary-data based Mendelian randomization identifies gene expression regulatory polymorphisms associated with bovine paratuberculosis by modulation of the nuclear factor Kappa Ξ² (NF-ΞΊΓ)-mediated inflammatory response. | Badia-BringuΓ© G et al. | β | 2023 | β |
| The eQTL colocalization and transcriptome-wide association study identify potentially causal genes responsible for economic traits in Simmental beef cattle. | Cai W et al. | β | 2023 | β |
| The genetic and evolutionary basis of gene expression variation in East Africans. | Kelly DE et al. | β | 2023 | β |
| A flexible summary statistics-based colocalization method with application to the mucin cystic fibrosis lung disease modifier locus. | Wang F et al. | β | 2022 | β |
| A multi-tissue atlas of regulatory variants in cattle. | Liu S et al. | β | 2022 | β |
| Amygdala and anterior cingulate transcriptomes from individuals with bipolar disorder reveal downregulated neuroimmune and synaptic pathways. | Zandi PP et al. | β | 2022 | β |
| Analyses of rare predisposing variants of lung cancer in 6,004 whole genomes in Chinese. | Wang C et al. | β | 2022 | β |
| Analysis of the caudate nucleus transcriptome in individuals with schizophrenia highlights effects of antipsychotics and new risk genes. | Benjamin KJM et al. | β | 2022 | β |
| A resource for integrated genomic analysis of the human liver. | Zhou YH et al. | β | 2022 | β |
| Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease. | Castaldi PJ et al. | β | 2022 | β |
| Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders. | Bryois J et al. | β | 2022 | β |
| Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of <i>MUC5B</i> and <i>DSP</i> in Idiopathic Pulmonary Fibrosis. | Borie R et al. | β | 2022 | β |
| Contribution and clinical relevance of germline variation to the cancer transcriptome. | Pereira B et al. | β | 2022 | β |
| Disentangling genetic feature selection and aggregation in transcriptome-wide association studies. | Cao C et al. | β | 2022 | β |
| Enhancing discoveries of molecular QTL studies with small sample size using summary statistic imputation. | Wang T et al. | β | 2022 | β |
| Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. | Maihofer AX et al. | β | 2022 | β |
| Epigenome-wide association study of lung function in Latino children and youth with asthma. | Herrera-Luis E et al. | β | 2022 | β |
| Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. | Liu H et al. | β | 2022 | β |
| eQTL mapping using allele-specific count data is computationally feasible, powerful, and provides individual-specific estimates of genetic effects. | Zhabotynsky V et al. | β | 2022 | β |
| ezQTL: A Web Platform for Interactive Visualization and Colocalization of QTLs and GWAS Loci. | Zhang T et al. | β | 2022 | β |
| Functional Characterization of Genetic Variant Effects on Expression. | Flynn ED et al. | β | 2022 | β |
| Functional dissection of inherited non-coding variation influencing multiple myeloma risk. | Ajore R et al. | β | 2022 | β |
| Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease. | Gong J et al. | β | 2022 | β |
| Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. | Moore A et al. | β | 2022 | β |
| Genomic innovation and regulatory rewiring during evolution of the cotton genus Gossypium. | Wang M et al. | β | 2022 | β |
| GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements. | Dixon PH et al. | β | 2022 | β |
| Heterozygous Tropomodulin 3 mice have improved lung vascularization after chronic hypoxia. | Stobdan T et al. | β | 2022 | β |
| Human pancreatic islet miRNA-mRNA networks of altered miRNAs due to glycemic status. | Karagiannopoulos A et al. | β | 2022 | β |
| Impact of internal brand management on sustainable competitive advantage: An explanatory study based on the mediating roles of brand commitment and brand citizenship behavior. | Qureshi FN et al. | β | 2022 | β |
| Impaired type I interferon signaling activity implicated in the peripheral blood transcriptome of preclinical Alzheimer's disease. | Song L et al. | β | 2022 | β |
| Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk. | Lopez S et al. | β | 2022 | β |
| Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain. | Vialle RA et al. | β | 2022 | β |
| <i>BIRC6</i> modifies risk of invasive bacterial infection in Kenyan children. | Gilchrist JJ et al. | β | 2022 | β |
| Mendelian randomization analyses implicate biogenesis of translation machinery in human aging. | Javidnia S et al. | β | 2022 | β |
| Multi-ancestry genome-wide association study of asthma exacerbations. | Herrera-Luis E et al. | β | 2022 | β |
| Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Sajuthi SP et al. | β | 2022 | β |
| PCA outperforms popular hidden variable inference methods for molecular QTL mapping. | Zhou HJ et al. | β | 2022 | β |
| Plasma proteome analyses in individuals of European and African ancestry identify cis-pQTLs and models for proteome-wide association studies. | Zhang J et al. | β | 2022 | β |
| Powerful eQTL mapping through low-coverage RNA sequencing. | Schwarz T et al. | β | 2022 | β |
| Random field modeling of multi-trait multi-locus association for detecting methylation quantitative trait loci. | Lyu C et al. | β | 2022 | β |
| RNA editing underlies genetic risk of common inflammatory diseases. | Li Q et al. | β | 2022 | β |
| Single-cell dissection of the obesity-exercise axis in adipose-muscle tissues implies a critical role for mesenchymal stem cells. | Yang J et al. | β | 2022 | β |
| Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development. | Dredge WH et al. | β | 2022 | β |
| The activity of human enhancers is modulated by the splicing of their associated lncRNAs. | Tan JY et al. | β | 2022 | β |
| The Carbon Footprint of Bioinformatics. | Grealey J et al. | β | 2022 | β |
| The regulatory landscape of multiple brain regions in outbred heterogeneous stock rats. | Munro D et al. | β | 2022 | β |
| A 584Β bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer. | Jermusyk A et al. | β | 2021 | β |
| A compendium of uniformly processed human gene expression and splicing quantitative trait loci. | Kerimov N et al. | β | 2021 | β |
| Alignment of single-cell RNA-seq samples without overcorrection using kernel density matching. | Chen M et al. | β | 2021 | β |
| Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus. | Colli LM et al. | β | 2021 | β |
| A molecular quantitative trait locus map for osteoarthritis. | Steinberg J et al. | β | 2021 | β |
| An Empirical Bayes approach for the identification of long-range chromosomal interaction from Hi-C data. | Zhang Q et al. | β | 2021 | β |
| An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease. | Cohain AT et al. | β | 2021 | β |
| A pipeline for RNA-seq based eQTL analysis with automated quality control procedures. | Wang T et al. | β | 2021 | β |
| A scalable unified framework of total and allele-specific counts for cis-QTL, fine-mapping, and prediction. | Liang Y et al. | β | 2021 | β |
| Assigning Co-Regulated Human Genes and Regulatory Gene Clusters. | Strunz T et al. | β | 2021 | β |
| Benchmarking sequencing methods and tools that facilitate the study of alternative polyadenylation. | Shah A et al. | β | 2021 | β |
| Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis. | AygΓΌn N et al. | β | 2021 | β |
| CCmed: cross-condition mediation analysis for identifying replicable trans-associations mediated by cis-gene expression. | Yang F et al. | β | 2021 | β |
| Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms. | Zhang T et al. | β | 2021 | β |
| Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion. | Hu M et al. | β | 2021 | β |
| Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain. | Liang L et al. | β | 2021 | β |
| Dynamic effects of genetic variation on gene expression revealed following hypoxic stress in cardiomyocytes. | Ward MC et al. | β | 2021 | β |
| Dynamic landscape of immune cell-specific gene regulation in immune-mediated diseases. | Ota M et al. | β | 2021 | β |
| Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci. | Breeze CE et al. | β | 2021 | β |
| Gene Expression Analysis in Three Posttraumatic Stress Disorder Cohorts Implicates Inflammation and Innate Immunity Pathways and Uncovers Shared Genetic Risk With Major Depressive Disorder. | Garrett ME et al. | β | 2021 | β |
| Genetic Dissection of Temperament Personality Traits in Italian Isolates. | Concas MP et al. | β | 2021 | β |
| Genetic drivers of m<sup>6</sup>A methylation in human brain, lung, heart and muscle. | Xiong X et al. | β | 2021 | β |
| Genetic Effects on Transcriptome Profiles in Colon Epithelium Provide Functional Insights for Genetic Risk Loci. | DΓez-Obrero V et al. | β | 2021 | β |
| Genetic impacts on DNA methylation: research findings and future perspectives. | VillicaΓ±a S et al. | β | 2021 | β |
| Genetic variants shape rheumatoid arthritis-specific transcriptomic features in CD4<sup>+</sup> T cells through differential DNA methylation, explaining a substantial proportion of heritability. | Ha E et al. | β | 2021 | β |
| Genome-wide contribution of common Short-Tandem Repeats to Parkinsonβs Disease genetic risk | Bustos BI et al. | β | 2021 | β |
| Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. | Yang C et al. | β | 2021 | β |
| Haplotype-resolved diverse human genomes and integrated analysis of structural variation. | Ebert P et al. | β | 2021 | β |
| Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. | Bonder MJ et al. | β | 2021 | β |
| Identification of tissue-specific and common methylation quantitative trait loci in healthy individuals using MAGAR. | Scherer M et al. | β | 2021 | β |
| Inferring recombination patterns in African populations. | van Eeden G et al. | β | 2021 | β |
| Integrative genomics analysis reveals a 21q22.11 locus contributing risk to COVID-19. | Ma Y et al. | β | 2021 | β |
| Joint eQTL mapping and inference of gene regulatory network improves power of detecting both cis- and trans-eQTLs. | Zhou X et al. | β | 2021 | β |
| Local adaptation and archaic introgression shape global diversity at human structural variant loci. | Yan SM et al. | β | 2021 | β |
| Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments. | Sheng X et al. | β | 2021 | β |
| MOCCASIN: a method for correcting for known and unknown confounders in RNA splicing analysis. | Slaff B et al. | β | 2021 | β |
| Multi-Omics Approaches to Define Calcific Aortic Valve Disease Pathogenesis. | Blaser MC et al. | β | 2021 | β |
| Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus. | Soliai MM et al. | β | 2021 | β |
| Optimizing expression quantitative trait locus mapping workflows for single-cell studies. | Cuomo ASE et al. | β | 2021 | β |
| Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation. | Jerber J et al. | β | 2021 | β |
| Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. | de Goede OM et al. | β | 2021 | β |
| Privacy-preserving genotype imputation in a trusted execution environment. | Dokmai N et al. | β | 2021 | β |
| Proteome-wide Systems Genetics to Identify Functional Regulators of Complex Traits. | Molendijk J et al. | β | 2021 | β |
| Psychosocial experiences modulate asthma-associated genes through gene-environment interactions. | Resztak JA et al. | β | 2021 | β |
| Rare variants regulate expression of nearby individual genes in multiple tissues. | Li J et al. | β | 2021 | β |
| Recent advances in functional annotation and prediction of the epitranscriptome. | Zhang SY et al. | β | 2021 | β |
| Selection-adjusted inference: an application to confidence intervals for cis-eQTL effect sizes. | Panigrahi S et al. | β | 2021 | β |
| Single-Cell Epigenomics and Functional Fine-Mapping of Atherosclerosis GWAS Loci. | Γrd T et al. | β | 2021 | β |
| Structural variants are a major source of gene expression differences in humans and often affect multiple nearby genes. | Scott AJ et al. | β | 2021 | β |
| The genetic architecture of DNA replication timing in human pluripotent stem cells. | Ding Q et al. | β | 2021 | β |
| The impact of cell type and context-dependent regulatory variants on human immune traits. | Mu Z et al. | β | 2021 | β |
| The intronic branch point sequence is under strong evolutionary constraint in the bovine and human genome. | Kadri NK et al. | β | 2021 | β |
| The role of genetic polymorphisms in STIM1 and ORAI1 for erythropoietin resistance in patients with renal failure. | Kao CC et al. | β | 2021 | β |
| TIGER: The gene expression regulatory variation landscape of human pancreatic islets. | Alonso L et al. | β | 2021 | β |
| Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. | Conti DV et al. | β | 2021 | β |
| TreeMap: a structured approach to fine mapping of eQTL variants. | Liu L et al. | β | 2021 | β |
| Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney. | Eales JM et al. | β | 2021 | β |
| Zika Virus Congenital Syndrome and <i>MTOR</i> gene variants: insights from a family of dizygotic twins. | de O da Silva LR et al. | β | 2021 | β |
| Alternative polyadenylation mediates genetic regulation of gene expression. | Mittleman BE et al. | β | 2020 | β |
| A mega-analysis of expression quantitative trait loci in retinal tissue. | Strunz T et al. | β | 2020 | β |
| An enhanced machine learning tool for cis-eQTL mapping with regularization and confounder adjustments. | Yan KK et al. | β | 2020 | β |
| An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations. | Kakuta Y et al. | β | 2020 | β |
| A second X chromosome contributes to resilience in a mouse model of Alzheimer's disease. | Davis EJ et al. | β | 2020 | β |
| Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts. | Mullin BH et al. | β | 2020 | β |
| DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data. | Jiang Y et al. | β | 2020 | β |
| Expression Quantitative Trait Loci (eQTL) Mapping in Korean Patients With Crohn's Disease and Identification of Potential Causal Genes Through Integration With Disease Associations. | Jung S et al. | β | 2020 | β |
| Fine-mapping and QTL tissue-sharing information improves the reliability of causal gene identification. | Barbeira AN et al. | β | 2020 | β |
| Gene expression variability in human and chimpanzee populations share common determinants. | Fair BJ et al. | β | 2020 | β |
| Genetic analyses support the contribution of mRNA N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) modification to human disease heritability. | Zhang Z et al. | β | 2020 | β |
| Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. | ViΓ±uela A et al. | β | 2020 | β |
| Genetic variants modulate gene expression statin response in human lymphoblastoid cell lines. | Theusch E et al. | β | 2020 | β |
| Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure. | Arvanitis M et al. | β | 2020 | β |
| In vivo functional analysis of non-conserved human lncRNAs associated with cardiometabolic traits. | Ruan X et al. | β | 2020 | β |
| lncRNAKB, a knowledgebase of tissue-specific functional annotation and trait association of long noncoding RNA. | Seifuddin F et al. | β | 2020 | β |
| Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma. | Choi J et al. | β | 2020 | β |
| Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. | Erzurumluoglu AM et al. | β | 2020 | β |
| Phenotypic and Molecular Characterization of Risk Loci Associated With Asthma and Lung Function. | Karaca M et al. | β | 2020 | β |
| Pleiotropic Locus 15q24.1 Reveals a Gender-Specific Association with Neovascular but Not Atrophic Age-Related Macular Degeneration (AMD). | Kiel C et al. | β | 2020 | β |
| Population-scale proteome variation in human induced pluripotent stem cells. | Mirauta BA et al. | β | 2020 | β |
| Properties of structural variants and short tandem repeats associated with gene expression and complex traits. | Jakubosky D et al. | β | 2020 | β |
| Quantile regression for challenging cases of eQTL mapping. | Sun B et al. | β | 2020 | β |
| Quantitative genetic analysis deciphers the impact of cis and trans regulation on cell-to-cell variability in protein expression levels. | Morgan MD et al. | β | 2020 | β |
| Regulatory mechanisms of major depressive disorder risk variants. | Li S et al. | β | 2020 | β |
| Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression. | Cuomo ASE et al. | β | 2020 | β |
| Systematic identification of functional SNPs interrupting 3'UTR polyadenylation signals. | Shulman ED et al. | β | 2020 | β |
| Systematic integrated analysis of genetic and epigenetic variation in diabetic kidney disease. | Sheng X et al. | β | 2020 | β |
| The GTEx Consortium atlas of genetic regulatory effects across human tissues. | GTEx Consortium | β | 2020 | β |
| The impact of sex on gene expression across human tissues. | Oliva M et al. | β | 2020 | β |
| Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium. | Sajuthi SP et al. | β | 2020 | β |
| Using regulatory variants to detect gene-gene interactions identifies networks of genes linked to cell immortalisation. | Wragg D et al. | β | 2020 | β |
| Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits. | Raulerson CK et al. | β | 2019 | β |
| A genome-wide association study implicates <i>NR2F2</i> in lymphangioleiomyomatosis pathogenesis. | Kim W et al. | β | 2019 | β |
| A multi-omics digital research object for the genetics of sleep regulation. | Jan M et al. | β | 2019 | β |
| Characterization of eQTLs associated with androstenone by RNA sequencing in porcine testis. | Drag MH et al. | β | 2019 | β |
| Characterizing human genomic coevolution in locus-gene regulatory interactions. | Savel D et al. | β | 2019 | β |
| Characterizing the Major Structural Variant Alleles of the Human Genome. | Audano PA et al. | β | 2019 | β |
| Chromatin three-dimensional interactions mediate genetic effects on gene expression. | Delaneau O et al. | β | 2019 | β |
| Combined genetic and transcriptome analysis of patients with SLE: distinct, targetable signatures for susceptibility and severity. | Panousis NI et al. | β | 2019 | β |
| Dectin-1 genetic deficiency predicts chronic lung allograft dysfunction and death. | Calabrese DR et al. | β | 2019 | β |
| eQTLMAPT: Fast and Accurate eQTL Mediation Analysis With Efficient Permutation Testing Approaches. | Wang T et al. | β | 2019 | β |
| Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms. | Liu B et al. | β | 2019 | β |
| Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human Liver. | ΓalΔ±Εkan M et al. | β | 2019 | β |
| Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci. | Gong J et al. | β | 2019 | β |
| Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms. | Walker RL et al. | β | 2019 | β |
| Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone. | Mullin BH et al. | β | 2019 | β |
| Genetic variant rs17185536 regulates <i>SIM1</i> gene expression in human brain hypothalamus. | Liu G et al. | β | 2019 | β |
| Genome-Wide Genotype-Expression Relationships Reveal Both Copy Number and Single Nucleotide Differentiation Contribute to Differential Gene Expression between Stickleback Ecotypes. | Huang Y et al. | β | 2019 | β |
| High-Dimensional Bayesian Network Inference From Systems Genetics Data Using Genetic Node Ordering. | Wang L et al. | β | 2019 | β |
| Laser capture microdissection of human pancreatic islets reveals novel eQTLs associated with type 2 diabetes. | Khamis A et al. | β | 2019 | β |
| Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. | Hellwege JN et al. | β | 2019 | β |
| Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. | Lona-Durazo F et al. | β | 2019 | β |
| New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. | Evangelou E et al. | β | 2019 | β |
| Nuclear genetic regulation of the human mitochondrial transcriptome. | Ali AT et al. | β | 2019 | β |
| ORE identifies extreme expression effects enriched for rare variants. | Richter F et al. | β | 2019 | β |
| Prioritizing Parkinson's disease genes using population-scale transcriptomic data. | Li YI et al. | β | 2019 | β |
| Scaling computational genomics to millions of individuals with GPUs. | Taylor-Weiner A et al. | β | 2019 | β |
| Whole-Transcriptome Causal Network Inference with Genomic and Transcriptomic Data. | Wang L et al. | β | 2019 | β |
| Annotation-free quantification of RNA splicing using LeafCutter. | Li YI et al. | β | 2018 | β |
| A systems genetics resource and analysis of sleep regulation in the mouse. | Diessler S et al. | β | 2018 | β |
| Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. | Zhang T et al. | β | 2018 | β |
| Epigenome-Wide Analyses Identify Two Novel Associations With Recurrent Stroke in the Vitamin Intervention for Stroke Prevention Clinical Trial. | Davis Armstrong NM et al. | β | 2018 | β |
| Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia. | Bryois J et al. | β | 2018 | β |
| Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. | O'Brien HE et al. | β | 2018 | β |
| Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts. | Mullin BH et al. | β | 2018 | β |
| Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants. | Dadaev T et al. | β | 2018 | β |
| Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. | VΓ€limΓ€ki N et al. | β | 2018 | β |
| Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci. | Liu B et al. | β | 2018 | β |
| Impact of regulatory variation across human iPSCs and differentiated cells. | Banovich NE et al. | β | 2018 | β |
| Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS. | Pan DZ et al. | β | 2018 | β |
| Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. | Raj T et al. | β | 2018 | β |
| Molecular and functional variation in iPSC-derived sensory neurons. | Schwartzentruber J et al. | β | 2018 | β |
| Multi-omic Directed Networks Describe Features of Gene Regulation in Aged Brains and Expand the Set of Genes Driving Cognitive Decline. | Tasaki S et al. | β | 2018 | β |
| Power, false discovery rate and Winner's Curse in eQTL studies. | Huang QQ et al. | β | 2018 | β |
| Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. | Qiu C et al. | β | 2018 | β |
| Shared genetic effects on chromatin and gene expression indicate a role for enhancer priming in immune response. | Alasoo K et al. | β | 2018 | β |
| Trait Mapping Approaches Through Linkage Mapping in Plants. | Kulwal PL | β | 2018 | β |
| Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. | Gusev A et al. | β | 2018 | β |
| Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. | Gamazon ER et al. | β | 2018 | β |
| A complete tool set for molecular QTL discovery and analysis. | Delaneau O et al. | β | 2017 | β |
| Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization. | Haitjema S et al. | β | 2017 | β |
| C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis. | Lepik K et al. | β | 2017 | β |
| Decreased STARD10 Expression Is Associated with Defective Insulin Secretion in Humans and Mice. | Carrat GR et al. | β | 2017 | β |
| Diversity and regulatory impact of copy number variation in the primate Macaca fascicularis. | Gschwind AR et al. | β | 2017 | β |
| Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling. | Nariai N et al. | β | 2017 | β |
| Estimating the causal tissues for complex traits and diseases. | Ongen H et al. | β | 2017 | β |
| Genetic effects on gene expression across human tissues. | GTEx Consortium et al. | β | 2017 | β |
| Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. | Kim-Hellmuth S et al. | β | 2017 | β |
| Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease. | Ko YA et al. | β | 2017 | β |
| Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. | de Lange KM et al. | β | 2017 | β |
| Identification of breast cancer associated variants that modulate transcription factor binding. | Liu Y et al. | β | 2017 | β |
| Pan-cancer analysis of somatic copy-number alterations implicates IRS4 and IGF2 in enhancer hijacking. | Weischenfeldt J et al. | β | 2017 | β |
| Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues. | Brown AA et al. | β | 2017 | β |
| Quantifying the regulatory effect size of <i>cis</i>-acting genetic variation using allelic fold change. | Mohammadi P et al. | β | 2017 | β |
| The impact of structural variation on human gene expression. | Chiang C et al. | β | 2017 | β |
| The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression. | Liu NQ et al. | β | 2017 | β |
| The whole-genome landscape of medulloblastoma subtypes. | Northcott PA et al. | β | 2017 | β |
| Time-dependent genetic effects on gene expression implicate aging processes. | Bryois J et al. | β | 2017 | β |
| veqtl-mapper: variance association mapping for molecular phenotypes. | Brown AA | β | 2017 | β |
| An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants. | Davis JR et al. | β | 2016 | β |
| DRIMSeq: a Dirichlet-multinomial framework for multivariate count outcomes in genomics. | Nowicka M et al. | β | 2016 | β |
| Alternative Splicing QTLs in European and African Populations. | Ongen H et al. | β | 2015 | β |