ArticleNature methods2018
GeNets: a unified web platform for network-based genomic analyses.
Article in Nature methods, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
37 citing papers in PubMed.
- Article
- MicrobiomeStatPlots: Microbiome statistics plotting gallery for meta-omics and bioinformatics.iMeta · 2025Article
- Article
- Context-defined cancer co-dependency mapping identifies a functional interplay between PRC2 and MLL-MEN1 complex in lymphoma.Nature communications · 2023Article
- A Rare but Aggressive Malignancy: A Case Report of a Gastrointestinal Neuroectodermal Tumor (GNET).Cureus · 2023Article
- Artificial Intelligence: A Promising Tool in Exploring the Phytomicrobiome in Managing Disease and Promoting Plant Health.Plants (Basel, Switzerland) · 2023Review
- Protein interaction studies in human induced neurons indicate convergent biology underlying autism spectrum disorders.Cell genomics · 2023Article
- Islet Gene View-a tool to facilitate islet research.Life science alliance · 2022Article
- Integrating human brain proteomes with genome-wide association data implicates novel proteins in post-traumatic stress disorder.Molecular psychiatry · 2022Article
- Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets.Genome biology · 2022Article
- A human-based multi-gene signature enables quantitative drug repurposing for metabolic disease.eLife · 2022Article
- Bioinformatics-based analysis of the association between the A1-chimaerin (Bioengineered · 2021Article
- TIGA: target illumination GWAS analytics.Bioinformatics (Oxford, England) · 2021Article
- DECO: a framework for jointly analyzing de novo and rare case/control variants, and biological pathways.Briefings in bioinformatics · 2021Article
- De novo variation in bipolar disorder.Molecular psychiatry · 2021Article
- A machine learning approach to brain epigenetic analysis reveals kinases associated with Alzheimer's disease.Nature communications · 2021Article
- Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.PLoS genetics · 2021Article
- Brain proteome-wide association study implicates novel proteins in depression pathogenesis.Nature neuroscience · 2021Article
- Application of Deep Learning in Plant-Microbiota Association Analysis.Frontiers in genetics · 2021Review
- TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci.Human molecular genetics · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
25 authors.
Funding
Abstract
Functional genomics networks are widely used to identify unexpected pathway relationships in large genomic datasets. However, it is challenging to compare the signal-to-noise ratios of different networks and to identify the optimal network with which to interpret a particular genetic dataset. We present GeNets, a platform in which users can train a machine-learning model (Quack) to carry out these comparisons and execute, store, and share analyses of genetic and RNA-sequencing datasets.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.