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Data was scraped using ScraperWiki and refined with Google Refine; the resultant tables were merged using Google Fusion and finally visualised through Batchgeo.
Images were merged using Metamorph 6.1 imaging software (Downingtown, PA).
The 100 bp of overlapping paired-end reads were merged using PandaSeq (version 2.7).
The acquired images were merged using Photoshop software to show specific cellular labeling.
Following [27], samples located in the same ROI were merged using the mean statistics.
Paired-end reads were merged using FLASH (V1.2.7) to splice overlapping sequences to raw tags (Magoč and Salzberg 2011).
Images were merged using Photoshop 6.0 (Adobe).
Images were merged using Volocity software (Improvision Inc).
Images were merged using Adobe Photoshop 5.0 software.
Similar top motifs were merged using uniqmotifs [11].
Confocal Z-series were merged using Zeiss software and images assembled for analysis using Adobe Photoshop.
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