Connect the Dots and See the Whole Picture with the Iso-Seq Method
With full-length transcript sequencing you will see the complete picture of isoform diversity in the human transcriptome. Reveal gene fusions, splice variants, and novel isoforms to uncover hidden biology.
The 2018 Iso-Seq SMRT Grant is Now Open!
Tell us how the Iso-Seq method will drive new discoveries in your research for a chance to win SMRTbell library construction (4 samples), PacBio sequencing (up to 8 Sequel SMRT Cells), and bioinformatics analysis.
One winner will be selected from all qualified applications by a panel of PacBio and RTL Genomics scientists.
Proposals will be accepted between May 1 – June 30, 2018. Read the official rules here.
Get inspired and learn how scientists are using the Iso-Seq Method to reveal new biology
- Simplified sequencing of full-length isoforms in cancer on the PacBio Sequel System
- Identification of differentially expressed splice variants by the proteogenomic pipeline Splicify
- SMRT Sequencing of full-length androgen receptor isoforms in prostate cancer reveals previously hidden drug resistant variants
- Characterization of fusion genes and the significantly expressed fusion isoforms in breast cancer by hybrid sequencing
Meet our SMRT Grant co-sponsor
RTLGenomics is a molecular sequencing laboratory that provides full service expertise from sample processing to comprehensive bioinformatics and biostatistics. We provide customized solutions for your sequencing needs and strive to deliver unparalleled customer service and turnaround time. In addition to being a PacBio Certified Service provider, we offer multiple sequencing platforms and services, helping to bridge the gap from concept to publication. Learn more about RTLGenomics, our SMRT Sequencing expertise and other provided services.