SureCall
SureCall 免費 NGS SureSelect HaloPlex 分析平台
Integrated data analysis for OneSeq Target Enrichment with simultaneous detection of genome-wide copy number changes, copy-neutral LOH, SNPs and Indels in one simplified workflow.
Optimized for the analysis of NGS data generated using HaloPlexHS with the incorporation of molecular barcodes, allowing for the identification of duplicate reads, hence significantly improving base calling accuracy even at low allelic frequencies compared to conventional NGS methods.
線上教學影片 軟體下載
硬體需求
| PC and Mac version | |
|---|---|
| Programs | Any program that enables you to open PDF files (for example, Adobe® Reader®) |
| Hard disk space | 500 GB (20 GB for genome reference data and annotation data and 480 GB for your sequencing data) |
| Display resolution | 1280 x 768 or higher |
| PC version | Minimum | Recommended |
|---|---|---|
| Operating system | 64-bit Windows 7 Enterprise or Windows 7 Professional | Same |
| Processor | > 2.0 GHz | > 3.0 GHz, 8-core |
| Working memory (RAM) | Without aligners installed: 8 GB With aligners installed: 12 GB |
Without aligners installed: 8 GB With aligners installed: 16 GB |
| Mac version | Minimum | Recommended |
|---|---|---|
| Operating system | Macintosh OS X Mountain Lion or Macintosh OS X Mavericks | Same |
| Processor | > 2.0 GHz dual-core Intel Core i5 | > 2.5 GHz dual-core Intel Core i7 |
| Working memory (RAM) | Without aligners installed: 8 GB With aligners installed: 12 GB |
Without aligners installed: 8 GB With aligners installed: 16 GB |
SureCall
- From alignment of raw data to categorization and annotation of mutations in three simple steps
- Supports four different types of analysis: Single Sample, Tumor-Normal, Trio and OneSeq CNV and Mutation Analysis
- Supports variant annotation from many public sources, including NCBI, COSMIC, PubMed, ClinVar and custom annotation
- Reduces time-to-results from days to hours without complex IT infrastructure or special hardware
- Addresses the needs of clinical researchers from analysis to reporting out of their target enrichment NGS data, eliminating data analysis as a bottleneck
說明書下載
使用手冊 |
回到頂端
威健代理
