Genomics Resources Core Facilities
Providing access to high-quality genomics services at affordable costs since 2000.
Our Services
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End-to-end sequencing project support.
Experimental design
Sequencing depth calculation
Budget plan
Sample extraction
Submission related technical issues and strategies.
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DNA and RNA sample quantification and quality assessment services across a wide range of sample types, sources, and extraction methods.
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Automated and manual preparation of DNA or RNA samples for Sequencing.
RNA-Seq, Capture-based RNA-Seq, miRNA-Seq, ChIP-Seq, WGS, WES, Customized Panel-Seq.
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Preparation and sequencing for scRNA-Seq, scATAC-Seq, scTCR/BCR, Multiome, On-Chip Multiplexing (OCM).
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Olink® proteomics profiling services for biomarker discovery and protein expression analysis using diverse sample types
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Sequencing for all kinds of libraries of amplicons, bulk RNA/DNA, single-cell RNA, panels.
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Sequencing for WGS, bulk RNA-seq, scRNA-seq, amplicon-seq, panel-seq.
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Primary, secondary, and tertiary data analysis.
A long-term solution for data delivery, storage, and management.
Our StoryThe Genomics Resources Core Facility (GRCF) at WCM, established in 2000, plays a pivotal role in advancing genomics research both internally and externally.
It offers a comprehensive range of services from experimental design and sample preparation to instrumentation, data analysis, interpretation, and validation.
At the core of its operations are cutting-edge sequencing technologies and a team of well-trained staff, enabling researchers to leverage state-of-the-art technologies effectively. These resources have not only supported but significantly contributed to numerous publications and successful grant applications within the research community.
The mission of the GRCF is clear: to provide access to high-quality genomics services at affordable costs, thereby fostering innovation and collaboration across the research landscape. By maintaining a commitment to excellence in service delivery and cost-effectiveness, the facility continues to play a critical role in advancing genomic research and its applications.
Available Instruments
10x Genomics Chromium X
SPT LabTech Firefly
Femto Pulse
Tapestation
QC System
QC System
NovaSeq X Plus
PacBio Revio
Short-Read Sequencer
Long-Read Sequencer
Automated Library Prep System
Single Cell Library Prep
For a full list of instruments click here.
Schedule your appointment today.
For user registration, sample submission, tracking and billing. Submit request and forms using an Agilent CrossLab/iLab Account.
Contact Us
Jenny Xiang, M.D.
Email: jzx2002@med.cornell.edu
Phone:
(212) 746-4258 (O)
(212) 746-6238/5076 (Lab)