The DNA Technologies and Expression Analysis Cores at the Genome Center offer high-throughput sequencing, genotyping, and microarray services, as well as training and consultation. Our goal is to enable access to high throughput genome-wide analyses at economical recharge rates, as a functional extension of your laboratory. We employ liquid handling robots to minimize sample handling variation and to provide fast turnaround times. We are a designated Campus Research Core Facility!
We offer the two complementary Next Generation Sequencing (NGS) technologies: Illumina sequencing, and PacBio (long read) sequencing, and provide the full spectrum of sequencing options and a wide range of library prep services for both platforms. Genotyping is performed on the Fluidigm EP1 System for low to medium assay numbers, and Illumina Infinium arrays for high density array SNP genotyping. Gene expression analysis is carried out by RNA-seq on HiSeq sequencers and on Illumina Expression BeadChip arrays. Single-cell transcriptome and genome analyses are enabled by our Fludigm C1 instrument, generating cDNA or whole genome amplifications from over 500 individual cells.
We offer annual Illumina and PacBio sequencing library preparation workshops, consultations on project considerations and experimental design, and custom sequencing library prep solutions. The Core’s equipment (with exception of the sequencers and the genotyping systems) is available to scientists on campus as Shared Equipment for a small usage fee.
We operate one PacBio RSII, one Illumina HiSeq4000, one Illumina HiSeq2500, three MiSeqs, liquid handling robots (IntegenX’s Apollo and Caliper/PerkinElmer’s Sciclone NGS G3), a Covaris E220 sonicator for high-throughput sample preparation, and a Fluidigm EP1 system, Fluidigm Access Array, and Fluidigm C1 Single Cell Auto Prep Station. We maintain a LIMS that allows users fast access to sequence data.
Our neighbors at the Bioinformatics Core provide sequence data analysis, statistical evaluations, consulting, and training to help you get the most out of your data. Please contact us for joint consultations with the Bioinformatics Core staff and also for complete analysis packages including sequencing and bioinformatics (e.g. differential gene expression, variant calling).
Our Services Include:
- Illumina HiSeq 4000, HiSeq 2500, and MiSeq sequencing: all run types
- PacBio RSII sequencing
- Fluidigm EP1 Genotyping
- Illumina Infinium II Genotyping
- Illumina BeadChip Expression Array Analysis
- 10X Genomics (GemCode) Linked-Read-Sequencing
- Fluidigm Access Array targeted multiplexed amplifications
- PacBio long insert DNA sequencing and Iso-Seq RNA sequencing library preparations
- Illumina sequencing library preps, including:
- Genomic DNA library preps
- RNA-Seq library preps (poly-A enrichment or ribo-depletion)
- High-Throughput (HT) library preps (DNA or RNA; starting from 24 libraries)
- miRNA-Seq library preps
- Methyl-seq: WGBS (Whole Genome Bisulfite Seq) and RRBS (Reduced Representation Bisulfite Seq)
- Reduced representation library preps (e.g., genotyping by sequencing)
- Mate Pair library preps
- Library preps from ChIP samples
- Library pooling
- Nucleic acid QC (from single samples to 96-well plates)
- Nucleic acid and library quantification
- Blue Pippin nucleic acid size selection
Our Shared Equipment includes:
- Bioanalyzer – microcapillary nucleic acid fragment analysis for sample and library QC
- Caliper LabChip GX – a “high-throughput bioanalyzer” (1-384 samples)
- Caliper Sciclone G3 – liquid handler robot for high-throughput library preps (up to 96 samples at at a time)
- Covaris E220 – high-throughput sonicator (1-96 samples)
- Diagenode Bioruptor sonicator
- Diagenode Megaruptor – long insert size DNA shearing for PacBio library preps
- BluePippin – 50 bp to 50 Kb DNA automated size selection
- Fluidigm Access Array – target amplification for sequencing-ready library prep
- Fluidigm C1 Single Cell Auto Prep – single cell transcriptome analysis and whole genome analyses
- FilterMax F5 Plate Reader – DNA/RNA quantification
- Nanodrop – microvolume DNA/RNA quantification
The Shared Equipment page explains how to get trained.
Acknowledging Our Services
Please support us by acknowledging our services in your publications. We have received NIH funding for the purchase of some of our instruments and this support should be mentioned. Please add a sentence like this to your acknowledgments: “The sequencing was carried by the DNA Technologies and Expression Analysis Cores at the UC Davis Genome Center, supported by NIH Shared Instrumentation Grant 1S10OD010786-01.” Acknowledgments such as this constitute a big support for future NIH instrumentation grant applications. Please also see our FAQs.
Supporting Your Grant Applications
We support the generation of proof-of-principle data by providing seed grants (please see below) and by offering free-of-charge consultations.
We will happily provide Letters-Of-Support for your grant application. Please also see our Instrument List.
The Genome Center invites proposals for pilot projects that merit support by the Genome Center. These seed grants award up to $2,000 to spend at any of the Cores; it is also possible to apply for grants at multiple Cores. The Genome Center seed grants are available all year round. They are meant to either introduce UC Davis labs to high-throughput sequencing or genotyping methods, or to help establish new methods. They will fund up to $2000 per project. Equivalent pilot grants are also available through the Bioinformatics core. Please see: http://dnatech.genomecenter.ucdavis.edu/2014/07/31/2015-genome-center-cores-pilot-grant-program/ . A seed grant application should be about one page long and include an outline of the project including the planned data analysis, a sentence on how the project would fit in with the goals of the GC seed grants, a listing of the specific services to be provided by our Core, as well as a budget (including an account number in case the costs exceed the grant amount).
Associated Services By Collaborating Cores
- Bioinformatics: The Bioinformatics Core will help you with the data analysis of all data generated by our cores as well as with the statistical interpretation. We highly recommend joint consultations with us and the Bioinformatics Core staff while planning your research project.
- DNA and RNA sample isolation services can be arranged through the Taqman Core.
- 16S Sequencing: We sequence 16S libraries daily. The vast majority of these are customer prepared samples. We do not generate 16S libraries ourselves because UC Davis has a facility specializing in 16S analysis: The Host Microbe Biology Systems Core (HSMBC; also located in our building). The HSMBC offers a complete service ranging from DNA isolation, 16S amplification, sequencing (carried out by the DNA Tech Core), to data analysis. You can certainly also pick selected parts of their service that you would require. Please contact the HSMBC manager for details.
- Tilling By Sequencing: The TILLING Core carries out high-throughput mutation screening for rice, wheat, Arabidopsis, and tomato populations.
- Bionano Irys Whole Genome Mapping: The Luo-Lab at UC Davis is offering whole genome mapping services using the Bionano optical mapping technology. This is of special interest if the genome assembly for your organism of interest is already of high quality. Please inquire with Ming-Cheng Luo.
- Sanger Sequencing: The DNA Sequencing Facility will help you help you with all Sanger sequencing projects.
- Cancer Genomics: The Genomics Shared Resource on the Sacramento campus provides general genomics support and custom services for cancer studies.