ProbeLynx
ProbeLynx evaluates microarray probe sequences against current genomic sequence data to assess probe specificity and update gene and transcript functional annotations for accurate microarray-based transcript measurement.
Key Features:
- Probe Specificity Assessment: Accepts probe sequences in FASTA format (oligonucleotide or cDNA) and compares them to up-to-date genomic sequences to assess specificity and identify potential cross-hybridization with paralogous genes.
- Functional Annotation Updates: Integrates gene function annotations from Ensembl and TIGR to update transcript- and gene-level annotations associated with each probe.
- Tab-delimited Output: Produces results as a tab-delimited flat file for integration into spreadsheet applications or database management systems.
- Genomic Dataset Flexibility: Supports analyses for human, mouse, chicken, and bovine genomes and can be adapted to additional genomic datasets.
Scientific Applications:
- Microarray probe re-annotation: Re-annotating microarray probe sets to reflect current genomic sequences and gene predictions.
- Gene expression reliability: Reducing false signals in gene expression studies by identifying cross-hybridizing probes and updating probe-target mappings.
- Transcriptomics and functional genomics: Facilitating analyses in genomics, transcriptomics, and functional genomics across human, mouse, chicken, and bovine datasets.
Methodology:
Compares input FASTA probe sequences (oligonucleotide or cDNA) to genomic sequence data to assess specificity and detect paralogous cross-hybridization, integrates Ensembl and TIGR gene function annotations, and outputs results as a tab-delimited flat file.
Topics
Details
- Maturity:
- Legacy
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 2/10/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Roche FM, Hokamp K, Acab M, Babiuk LA, Hancock REW, Brinkman FSL. ProbeLynx: a tool for updating the association of microarray probes to genes. Nucleic Acids Research. 2004;32(Web Server):W471-W474. doi:10.1093/nar/gkh452. PMID:15215432. PMCID:PMC441590.