Genomics Resources Core Facility
The Genomics Resources Core Facility (GRCF) was established in 2000 and provides genomics technologies and related high-throughput technologies to the basic and translational research and clinical communities, including Weill Cornell Medicine, NewYork-Presbyterian Hospital, the Hospital for Special Surgery, and external collaborators. The full-range and high quality of Next Generation Sequencing (NGS) services include experimental design, sample manipulation, instrumentation, data analysis/interpretation, and validation. We strive to provide cutting-edge, high-quality services at affordable costs to the entire research community.
Core Technologies/Services
- Consultation
- Sample collection and quality control
- Library construction (manual and robot) and sequencing
- Single-cell library preparation and sequencing
- Genomics data analysis, management and all bioinformatics support
- Support letter and writing genomics part for Principal Investigators’ grant and manuscript preparations
Equipment
- Pacbio Revio long-read Sequencer
- Illumina high throughput NovaSeq X-Plus Sequencer
- Illumina mid throughput NextSeq2000, and NextSeq500 sequencers
- Illumina low throughput MiSeq sequencer
- Covaris High-Performance Focused-ultrasonicator R230, and Diagenode Megaruptor 3
- Sage Science Pippin HT system
- Agilent 2100 Bioanalyzer, 4200 TapeStation and Femto Pulse
- Thermo Fisher Scientific NanoDrop 8000 Spectrophotometer and Qubit Fluorometer
- BioTek Synergy Neo2S Multi-Mode Reader
- Agilent NGS workstation Bravo B, Eppendorf epMotion 5075m and SPT Firefly automated liquid handling robot
- 10x Genomics Chromium Controller and Chromium X
- Life Technologies Quantstudio 6 Flex real-time PCR system