Human Genomic data support
GenoMiner H works only with human genomic data. It serves your data analysis needs from beginning to end, that is, from raw data to annotated lists, pathways and impressive graphs and diagrams. All available external human databases that offer annotation possibilities with your experimental results are integrated into GenoMiner H and you can utilize these during the analysis process. GenoMiner-H is not equipped with a pile of preconfigured workflows for genomic data analysis, because chances are that none of the general workflows are able to process your research data exactly the way you want it to. | |
With 4 terabytes of hard disk space as standard (up to 2048 TB optional) GenoMiner H provides sufficient storage capacity for all research applications. By using RAID architecture your valuable data is kept securely on the machine. Data access and communication are secured and encrypted to avoid misuse of your important assets.
| | User experience
GenoMiner H's web-based user interface is very easy to use. It even works with tablets or smartphones to enable you to control your GenoMiner H from any place. Your chosen data analysis package is tailor made for your specific needs. You do not need to worry about adjusting different parameters, just use set default values that are safe, secure and convenient. You can use the product right out-of-the-box, without worrying about drivers, parameters and options that makes many bioinformatics tools difficult to use. Support
By integrating our hardware, software and services, we can minimize your transition time and costs, helping you improve your research productivity. All GenoMiner H products come with
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Analysis Packages
Astrid offers five different human data analysis packages: SNP / InDel detection; CNV and structural variant analysis; ChIP-Seq analysis; mRNA expression analysis and miRNA expression analysis. Each package is made up of several consecutive applications that can be run and checked independently.
| DNA BASED | RNA BASED | ||||
| Task List | SNP; InDel detection | CNV and structural variant analysis | Chip-Seq analysis | mRNA expression, sequence analysis | miRNA expression, sequence analysis |
| Quality Assesment | | | | | |
| Alignment | | | | ||
| Spliced alignment | | ||||
| Adaptor trimming | | ||||
| Detection of known microRNAs | | ||||
| Mapping against transcribed sequences | | ||||
| Filtering | | | | ||
| CNV detection | | ||||
| Variant calling | | | | | |
| Peak detection | | ||||
| Transcript assembly | | | |||
| Expression analysis | | | |||
| Viewer | | | | | |
| Annotation | | | | | |
| Statistics | | | | | |
| Multi genome comparison | | | | ||
| Multi sample comparison | | | |||