Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genopyc: a Python library for investigating the functional effects of genomic variants associated to complex diseases.

Bioinformatics (Oxford, England) - 3 Jun 2024

Gualdi Francesco, Oliva Baldomero, Piñero Janet

Abstract excerpt

MOTIVATION: Integrative Biomedicl Informatics, Research Program on Biomedical Informatics (IBI - GRIB), Hospital Del Mar Medical Research Institute (IMIM), Department of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF) C/ del Dr. Aiguader 88 Barcelona 08003 Spain.Understanding the genetic basis of complex diseases is one of the main challenges in modern genomics. However, current tools often lack...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Computational Biology
Share to Data Mining
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genome-Wide Association Study

Share to Genomics

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 38889282
DOI: 10.1093/bioinformatics/btae379
PMCID: PMC11211212

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genopyc: a Python library for investigating the functional effects of genomic variants associated to complex diseases.PMID 38889282Read ↗

Genopyc: a python library for investigating the genomic basis of complex diseasesSemantic proximity Read ↗

IDEAL-GENOM: Integrated Downstream Analytical Toolkit for Genomic AnalysisSemantic proximity Read ↗

PhenoScanner: a database of human genotype-phenotype associations.Semantic proximity Read ↗

Polympact: exploring functional relations among common human genetic variants.Semantic proximity Read ↗

Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis.Semantic proximity Read ↗

GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and AnalysisSemantic proximity Read ↗

NeuroVar: An Open-source Tool for Gene Expression and Variation Data Visualization for Biomarkers of Neurological DiseasesSemantic proximity Read ↗

Integration of genomic variation and phenotypic data using HmtPhenomeSemantic proximity Read ↗

PhenoExam: an R package and Web application for the examination of phenotypes linked to genes and gene setsSemantic proximity Read ↗

Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.Semantic proximity Read ↗

JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene-variant discovery, annotation, prediction, and genotyping.Semantic proximity Read ↗

CoMut: Visualizing integrated molecular information with comutation plotsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.