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Signalmap v 1

Manufactured by Roche
Sourced in Switzerland, United States

SignalMap V.1.9 is a software application designed for data analysis and visualization. It offers tools for signal processing and mapping, catering to the needs of researchers and scientists working with various types of data.

Automatically generated - may contain errors

2 protocols using signalmap v 1

1

Comparative Microarray Analysis of Tumor DNA

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For each sample having sufficient quality and quantity, 700 to 1000 ng of tumor DNA and reference DNA were labeled, purified, and co-hybridized in equal quantity either to the NimbleGen Arrays (Roche, Basel, Switzerland) or Agilent Microarrays (Agilent Technologies, Santa Clara, CA, USA), during 12 to 24 h. Male and female human reference DNA were extracted from human blood for those analyzed on a NimbleGen support, whereas references were provided in the Agilent Kit for those analyzed on an Agilent support. Arrays were washed and scanned according to the technique-specific guidelines.
For samples processed with the Nimblegen technology, images were acquired on a GenePix 4000B scanner with the GenePix V.6.6 software (Molecular Devices, San Jose, CA, USA), and data was extracted using the NimbleScan V.2.5 software. Files produced by the NimbleScan software were then analyzed on SignalMap V.1.9 (Roche, Basel, Switzerland).
For samples processed with the Agilent technology, images were acquired on a SureScan Microarray Scanner using CytoScan software V.2.7, and then analyzed on CytoGenomics software V.3.0.2.11 (Thermo Fisher Scientific, Waltham, MA, USA).
For each sample, the quality of the analysis was evaluated subjectively based on the cytogenetic profile dynamism, the sex mismatch, and the degree of dispersion.
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2

Chromosome 3 and 8 Status-Based Risk Classification

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DNAs were obtained from snap-frozen samples according to standard procedures (proteinase K/RNAseA treatment and phenol/chloroform extraction using PLGL (Eppendorf, Hamburg, Germany), then qualified and quantified with a Nanodrop and a Qubit dsDNA BR Kit (Thermo Scientific, Wilmington USA). Up to 1μg tumour and reference DNA were labelled and cohybridised to the NimbleGen or Agilent Microarrays. The slides were washed and scanned according to the manufacturers' instructions. Images were acquired, data extracted and produced files analysed on suitable devices and softwares (For Nimblegen: GenePix 4000B, V.6.6 Software, NimbleScan V.2.5, SignalMap V.1.9 (Roche NimbleGen Inc. Madison USA); For Agilent: SureScan, CytoScan V.2.7, CytoGenomics V.2.7 (Agilent Technologies, Santa Clara, USA). The quality of aCGH was assessed on Log2(R) standard deviation, smoothing signal and sex mismatch. Then, patients were classified according to the status of chromosome 3 (disomy "D" or monosomy "M") and chromosome 8 (normal "nl", or with any type of gain "g"). Four risk classifications were defined as Low Risk: "D3/8nl", Intermediate Risk: "D3/8g"and "M3/8nl", High Risk: "M3/8g" based on the work of Cassoux et al. [21] .
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