![Researchers use a combination of third generation long-read RNA sequencing technology and short-read RNAseq to characterize the splicing landscape of prostate cancer | RNA-Seq Blog Researchers use a combination of third generation long-read RNA sequencing technology and short-read RNAseq to characterize the splicing landscape of prostate cancer | RNA-Seq Blog](https://www.rna-seqblog.com/wp-content/uploads/2017/12/long.png)
Researchers use a combination of third generation long-read RNA sequencing technology and short-read RNAseq to characterize the splicing landscape of prostate cancer | RNA-Seq Blog
![Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses | Semantic Scholar Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c3745aa0ffa5eb7690575e9a83496d7799f6bf2e/4-Figure2-1.png)
Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses | Semantic Scholar
![Long-read sequencing for identification of insertion sites in large transposon mutant libraries | Scientific Reports Long-read sequencing for identification of insertion sites in large transposon mutant libraries | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-022-07557-x/MediaObjects/41598_2022_7557_Fig1_HTML.png)
Long-read sequencing for identification of insertion sites in large transposon mutant libraries | Scientific Reports
![Stanford Scientists Report First Use of PacBio Whole Genome Sequencing to Identify a Disease-Causing Mutation - PacBio Stanford Scientists Report First Use of PacBio Whole Genome Sequencing to Identify a Disease-Causing Mutation - PacBio](https://www.pacb.com/wp-content/uploads/Figure-1-1-1024x367.png)
Stanford Scientists Report First Use of PacBio Whole Genome Sequencing to Identify a Disease-Causing Mutation - PacBio
Major short-read and long-read sequencing technologies. (A) Illumina... | Download Scientific Diagram
![HudsonAlpha researchers use highly accurate long-read sequencing technology to help diagnose rare disease – HudsonAlpha Institute for Biotechnology HudsonAlpha researchers use highly accurate long-read sequencing technology to help diagnose rare disease – HudsonAlpha Institute for Biotechnology](https://hudsonalpha.org/wp-content/uploads/2021/02/short-read-2.png)
HudsonAlpha researchers use highly accurate long-read sequencing technology to help diagnose rare disease – HudsonAlpha Institute for Biotechnology
![New study illustrates benefits of long-read sequencing technology for precision oncology | Genome Sciences Centre New study illustrates benefits of long-read sequencing technology for precision oncology | Genome Sciences Centre](https://www.bcgsc.ca/sites/default/files/styles/full_article/public/2020-07/Nanopore%20germline%20SV.png?itok=4vajXXQ-)