XHM

XHM identifies potential cross-hybridization in DNA microarray experiments by comparing microarray probe sequences to an organism-specific transcriptome database to detect sequence similarities that can produce misleading hybridization signals.


Key Features:

  • Detection of Cross-Hybridizations: Identifies probes likely to hybridize to non-target transcripts caused by high sequence similarity between genes.
  • Probe–Transcriptome Sequence Comparison: Compares individual microarray probe sequences against a comprehensive organism-specific transcriptome database.
  • Algorithmic Sequence Analysis: Employs computational algorithms to assess sequence similarity and flag potential cross-hybridization events.
  • User-Adjustable Parameters: Provides configurable analysis parameters to modify sequence-matching criteria and thresholds.

Scientific Applications:

  • Validation of Microarray Results: Identifies potential cross-hybridizations to support verification of differentially expressed gene lists.
  • Enhanced Interpretation of Gene Expression Data: Supplies sequence-based evidence to refine interpretation of microarray-derived expression patterns.

Methodology:

Systematic comparison of microarray probe sequences against an organism-specific transcriptome database using algorithmic sequence-similarity analysis to identify and flag potential cross-hybridizations.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Flikka K, Yadetie F, Laegreid A, Jonassen I. XHM: A system for detection of potential cross hybridizations in DNA microarrays. BMC Bioinformatics. 2004;5(1). doi:10.1186/1471-2105-5-117. PMID:15333145. PMCID:PMC517492.

Documentation

Links