Genomics Resources Core Facilities

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

Our Services

End-to-end sequencing project design and support.
- Experimental design
- Budget plan
- Sample sources and extraction methods
- RNA/DNA quantity and quality measurement
- Sample library preparation methods
- Sequencing system selection, and depth calculation
- iLab system submission and related technical issues and strategies
- Data distribution and analysis
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, bulk TCR/BCR-seq, RNA-IP-seq
Cell capture, library preparation and sequencing for scRNA-Seq, scATAC-Seq, scTCR/BCR, Multiome v2, On-Chip Multiplexing (OCM), GEM-X Flex v2.
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 and Olink Protein Sequencing.
PacBio Revio system for WGS and metagenome sequencing, bulk RNA-seq, scRNA-seq, amplicon-seq, PureTarget repeat expansion panel-seq, Fiber-seq (EpiCypher), Native 5mC and 5hmC calls. Multi-use SMRT Cells SPRQ-Nx Chemistry (4x3)
Support for RNA sequencing, DNA sequencing, single-cell sequencing, chromatin profiling, immune repertoire sequencing, long-read sequencing, and Olink protein profiling data.
Analysis planning, standard data processing, customized downstream analysis, result review, visualization, and grant/publication-related analysis support.
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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.