pubmed-article:15201182 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15201182 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
pubmed-article:15201182 | lifeskim:mentions | umls-concept:C1511726 | lld:lifeskim |
pubmed-article:15201182 | lifeskim:mentions | umls-concept:C1948044 | lld:lifeskim |
pubmed-article:15201182 | lifeskim:mentions | umls-concept:C2931151 | lld:lifeskim |
pubmed-article:15201182 | pubmed:issue | 18 | lld:pubmed |
pubmed-article:15201182 | pubmed:dateCreated | 2004-12-13 | lld:pubmed |
pubmed-article:15201182 | pubmed:abstractText | SUMMARY: We describe a tool, called aCGH-Smooth, for the automated identification of breakpoints and smoothing of microarray comparative genomic hybridization (array CGH) data. aCGH-Smooth is written in visual C++, has a user-friendly interface including a visualization of the results and user-defined parameters adapting the performance of data smoothing and breakpoint recognition. aCGH-Smooth can handle array-CGH data generated by all array-CGH platforms: BAC, PAC, cosmid, cDNA and oligo CGH arrays. The tool has been successfully applied to real-life data. AVAILABILITY: aCGH-Smooth is free for researchers at academic and non-profit institutions at http://www.few.vu.nl/~vumarray/. | lld:pubmed |
pubmed-article:15201182 | pubmed:language | eng | lld:pubmed |
pubmed-article:15201182 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15201182 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15201182 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15201182 | pubmed:month | Dec | lld:pubmed |
pubmed-article:15201182 | pubmed:issn | 1367-4803 | lld:pubmed |
pubmed-article:15201182 | pubmed:author | pubmed-author:MarchioriElen... | lld:pubmed |
pubmed-article:15201182 | pubmed:author | pubmed-author:YlstraBaukeB | lld:pubmed |
pubmed-article:15201182 | pubmed:author | pubmed-author:MeijerGerritG | lld:pubmed |
pubmed-article:15201182 | pubmed:author | pubmed-author:JongKeesK | lld:pubmed |
pubmed-article:15201182 | pubmed:author | pubmed-author:VaartA V DAV | lld:pubmed |
pubmed-article:15201182 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15201182 | pubmed:day | 12 | lld:pubmed |
pubmed-article:15201182 | pubmed:volume | 20 | lld:pubmed |
pubmed-article:15201182 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15201182 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15201182 | pubmed:pagination | 3636-7 | lld:pubmed |
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pubmed-article:15201182 | pubmed:meshHeading | pubmed-meshheading:15201182... | lld:pubmed |
pubmed-article:15201182 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:15201182 | pubmed:articleTitle | Breakpoint identification and smoothing of array comparative genomic hybridization data. | lld:pubmed |
pubmed-article:15201182 | pubmed:affiliation | Faculty of Sciences, Vrije Universiteit, De Boelelaan 1117, Amsterdam 1081HV, The Netherlands. cjong@few.vu.nl <cjong@few.vu.nl> | lld:pubmed |
pubmed-article:15201182 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:15201182 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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