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

A Systems Biology Interpretation of Array Comparative Genomic Hybridization (aCGH) Data through Phylogenetics.

Omics : a journal of integrative biology - 1 Mar 2016

Abunimer Ayman N, Salazar Jose, Noursi David P, Abu-Asab Mones S

Abstract excerpt

Array Comparative Genomic Hybridization (aCGH) is a rapid screening technique to detect gene deletions and duplications, providing an overview of chromosomal aberrations throughout the entire genome of a tumor, without the need for cell culturing. However, the heterogeneity of aCGH data obfuscates existing methods of data analysis. Analysis of aCGH data from a systems biology perspective or in the context of...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to Genome, Human

Share to Neoplasm Proteins

Share to Oligonucleotide Array Sequence Analysis

Share to Software

Share to Systems Biology

Source

Open in PubMed Open full text

Identifiers

PMID: 26983023
DOI: 10.1089/omi.2015.0184
PMCID: PMC4799695

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

A Systems Biology Interpretation of Array Comparative Genomic Hybridization (aCGH) Data through Phylogenetics.PMID 26983023Read ↗

PhyloOncology: Understanding cancer through phylogenetic analysis.Semantic proximity Read ↗

Novel multisample scheme for inferring phylogenetic markers from whole genome tumor profiles.Semantic proximity Read ↗

Estimation of rearrangement phylogeny for cancer genomes.Semantic proximity Read ↗

Evolutionary medicine: A meaningful connection between omics, disease, and treatment.Semantic proximity Read ↗

Detection of divergent genes in microbial aCGH experiments.Semantic proximity Read ↗

Leveraging Comparative Phylogenetics for Evolutionary Medicine: Applications to Comparative OncologySemantic proximity Read ↗

CGHsweep: an algorithm for analyzing chromosomal aberrations in genome using aCGH profiles.Semantic proximity Read ↗

When cells rebel: a comparative genomics investigation into marsupial cancer susceptibility.Semantic proximity Read ↗

Molecular portraits and the family tree of cancer.Semantic proximity Read ↗

Patterns of chromosomal imbalances defines subgroups of breast cancer with distinct clinical features and prognosis. A study of 305 tumors by comparative genomic hybridization.Semantic proximity Read ↗

Adapting simultaneous analysis phylogenomic techniques to study complex disease gene relationships.Semantic proximity Read ↗

Microarray comparative genomic hybridisation analysis incorporating genomic organisation, and application to enterobacterial plant pathogens.Semantic proximity Read ↗

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