NextGENe Online Help : The NextGENe Sensitive Aneuploidy Detection Tool : Analyzing Samples with the NextGENe SAD Tool
Analyzing Samples with the NextGENe SAD Tool
After you are satisfied with your trained, and optionally, tested, model, you can use the model to analyze patient samples. As with control samples for a model, patient samples can be raw data files (.fasta, .fastq, or .fq files) or aligned data files (.bam files).If the files are BAM files, then they must be aligned to a Build 37 reference. You can run one a single analysis at a time or you can run multiple analyses at the same time. If you run multiple analyses, then the NextGENe SAD tool creates a processing queue for each analysis and the analyses are carried in the order that you initiated them in the tool.