Genomics Resources Core Facilities
Providing access to high-quality genomics services at affordable costs since 2000.
Our Services
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Staff consultation for assistance, options, and recommendations to optimize your experimental strategy.
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Quantification and Qualification on samples using the Qubit Flourometer, NanoDrop, Agilent Tapestation, or Bioanalyzer.
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Preparation of DNA or RNA samples for Genomic Sequencing.
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Single-cell 3' Library RNA-Seq Assays (GEM-X v4 kit)
Single-cell 5' Library RNA-Seq Assays (GEM-X v3 kit)
Single Cell Multiome ATAC + Gene Expression
Single Cell ATAC-Seq
Cell Multiplexing Library Construction (Additional to Single-cell 3' Lib prep)
Single Cell Human TCR / BCR Enrichment (Additional to Single-cell 5' Lib prep)
CRISPR Screening Library Construction (Additional to Single-cell 3' Lib prep)
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Item description
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For DNA:
Whole Genome Sequencing, Whole Exome Sequencing, PCR Amplicon, Metagenomics, ChIP-Seq, Targeted Sequencing (panel), Sequencing for CRISPR screening.
For RNA:
Whole Transcriptome Sequencing, Capture-Based RNA-Seq, miRNA-Seq.
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Item description
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)