CLC GENOMICS WORKBENCH ASSEMBLY REGISTRATION
CLC GENOMICS WORKBENCH ASSEMBLY SOFTWARE
CLC GENOMICS WORKBENCH ASSEMBLY LICENSE

Human Somatic Mutation Database (HSMD) – A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.

QIAGEN IPA – Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems.

CLC GENOMICS WORKBENCH ASSEMBLY SOFTWARE

Introducing QCI Interpret One, clinical decision support software with professional i. QCI Interpret One – Oncology variant interpretation just got more precise.Catalogue of Somatic Mutations in Cancer (COSMIC) – Explore the impact of somatic mutations in human cancer with the world’s largest and most comprehensive resource.

Pharmaceutical Development Bioinformatic Services.Clinical Analysis and Interpretation Services.QIAGEN Discovery Bioinformatics Services.QIAGEN CLC Genomics Workbench – QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.Human Gene Mutations Database (HGMD) – Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati.Clinical QKB (Clinical QIAGEN Knowledge Base).COSMIC (Catalogue of Somatic Mutations in Cancer).QIAGEN CLC Genomics Workbench (Desktop).Learn more about its role in oncogenesis and ac. Know your biomarkers: PRKD1 linked to head and neck cancer? – A new cancer gene, PRKD1, has been identified as defining a subset of head and neck cancers.Stop looking for a needle in a haystack – Easily accelerate biomarker and target discovery by exploring and interpreting your data with intuitive, visual biomarker identification too.Single-Cell Genomic Solutions – Explore our powerful solutions for the analysis and interpretation of single-cell gene expression analysis and genomics.Pharmaceutical Development – Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m.Research & Discovery – Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.First-time users of CLC Gx on our workstation computers must complete the Workstation Request Form.All USC users can freely access the software on our workstation computers.

Equipped with dual-CPU and 512GB RAM, one of our workstation computers is configured specifically to handle large data set and computationally intensive tasks such as de novo genome assembly and sequencing alignment.

Wilson Dental Library, the University Park Campus.

Norris Medical Library (RM203A), the Health Sciences Campus.

The software has been installed on multiple workstation computers:.

On workstation computers in the libraries.

CLC GENOMICS WORKBENCH ASSEMBLY REGISTRATION

Mandatory registration is required for installing CLC Gx on your computer. Please submit the Local Installation Request Form.

The computer must be connected to the USC network, either via Ethernet cable on campus or via USC VPN when using wireless (applies to both on- and off-campus wireless connections).

Minimum hardware requirement for de novo assembly, metagenomics, and raw reads alignment:: 32GB RAM and Intel i7-6700 or faster processor.

Minimum hardware requirement for general use: 16GB RAM and Intel i7-2600 or faster processor.

CLC GENOMICS WORKBENCH ASSEMBLY LICENSE

The license consists of TWO concurrent user seats. USC has licensed CLC Gx for the free use of USC faculty, students and staff.

Clc genomics workbench assembly