Roche Fiona M, Hokamp Karsten, Acab Michael, Babiuk Lorne A, Hancock Robert E W, Brinkman Fiona S L
Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada.
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W471-4. doi: 10.1093/nar/gkh452.
As genome sequence data and gene prediction improve, probes developed for a given microarray experiment should be continuously re-evaluated for their specificity for given genes. ProbeLynx(www.pathogenomics.ca/probelynx) is a new web service which uses current genomic sequence information to re-examine microarray probe specificity and provide annotation updates relevant to determining which gene(s) and transcript(s) are associated with a given probe. Probe sequences (either oligonucleotide- or cDNA-based) are uploaded in FASTA format and the results returned as a tab-delimited flat file for insertion into a spreadsheet application or database management system for further analysis. ProbeLynx has been initially developed to focus on arrays derived from human, mouse, chicken and bovine genomes, but may be expanded to handle other genomic datasets. ProbeLynx offers microarray users the important ability to continuously assess the potential of a probe to cross-hybridize to paralogous genes and the suitability of a given probe to investigate a transcript of interest. By also including the latest gene function annotation information in the output, ProbeLynx provides the critical first step in updating microarray data annotation.
随着基因组序列数据和基因预测技术的改进,为特定微阵列实验开发的探针应不断重新评估其对特定基因的特异性。ProbeLynx(www.pathogenomics.ca/probelynx)是一项新的网络服务,它利用当前的基因组序列信息重新检查微阵列探针的特异性,并提供与确定哪些基因和转录本与特定探针相关的注释更新。探针序列(基于寡核苷酸或cDNA)以FASTA格式上传,结果以制表符分隔的平面文件形式返回,以便插入电子表格应用程序或数据库管理系统进行进一步分析。ProbeLynx最初是为专注于源自人类、小鼠、鸡和牛基因组的阵列而开发的,但可能会扩展以处理其他基因组数据集。ProbeLynx为微阵列用户提供了一项重要功能,即能够持续评估探针与旁系同源基因交叉杂交的可能性,以及特定探针用于研究感兴趣转录本的适用性。通过在输出中还包含最新的基因功能注释信息,ProbeLynx为更新微阵列数据注释提供了关键的第一步。