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

omicsPrint: detection of data linkage errors in multiple omics studies.

Bioinformatics (Oxford, England) - 15 Jun 2018

van Iterson Maarten, Cats Davy, Hop Paul, Heijmans Bastiaan T

Abstract excerpt

Summary: OmicsPrint is a versatile method for the detection of data linkage errors in multiple omics studies encompassing genetic, transcriptome and/or methylome data. OmicsPrint evaluates data linkage within and between omics data types using genotype calls from SNP arrays, DNA- or RNA-sequencing data and includes an algorithm to infer genotypes from Illumina DNA methylation array data. The method uses...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to DNA Methylation
Share to Genomics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Storage and Retrieval

Share to Oligonucleotide Array Sequence Analysis

Share to Sequence Analysis, RNA

Share to Software

Share to Transcriptome

Source

Identifiers

PMID: 29420690
DOI: 10.1093/bioinformatics/bty062

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

omicsPrint: detection of data linkage errors in multiple omics studies.PMID 29420690Read ↗

SMaSH: Sample matching using SNPs in humans.Semantic proximity Read ↗

The Personal Genome Project-UK: an open access resource of human multi-omics dataSemantic proximity Read ↗

MODMatcher: multi-omics data matcher for integrative genomic analysis.Semantic proximity Read ↗

Methods of integrating data to uncover genotype-phenotype interactions.Semantic proximity Read ↗

Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.Semantic proximity Read ↗

Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes.Semantic proximity Read ↗

The Molecular Human – A Roadmap of Molecular Interactions Linking Multiomics Networks with Disease EndpointsSemantic proximity Read ↗

DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.Semantic proximity Read ↗

Genomic Data Sharing for Novel Mendelian Disease Gene Discovery: The Matchmaker Exchange.Semantic proximity Read ↗

Model-Free Linkage Analysis of a Binary Trait.Semantic proximity Read ↗

OmicsPred as a centralised resource for genetic prediction of multi-omic traitsSemantic proximity Read ↗

Statistical analysis of '-omics' data : developments and applicationsSemantic proximity Read ↗

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