Genomics Resources Core Facilities

Providing access to high-quality genomics services at affordable costs since 2000.

Our Services

  • End-to-end sequencing project support.

    • Experimental design

    • Sequencing depth calculation

    • Budget plan

    • Sample extraction

    • Submission related technical issues and strategies.

  • DNA and RNA sample quantification and quality assessment services across a wide range of sample types, sources, and extraction methods.

  • 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.

  • Preparation and sequencing for scRNA-Seq, scATAC-Seq, scTCR/BCR, Multiome, On-Chip Multiplexing (OCM).

  • Olink® proteomics profiling services for biomarker discovery and protein expression analysis using diverse sample types

  • Sequencing for all kinds of libraries of amplicons, bulk RNA/DNA, single-cell RNA, panels.

  • Sequencing for WGS, bulk RNA-seq, scRNA-seq, amplicon-seq, panel-seq.

  • Primary, secondary, and tertiary data analysis.

    A long-term solution for data delivery, storage, and management.

Our Story

The 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)