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
The Pathologist: Solving Rare Disease with SMRT Sequencing - PacBio
Error correction and assembly complexity of single molecule sequencing reads | bioRxiv
The variables for NGS experiments: coverage, read length, multiplexing
Long-Read Sequencing – A Powerful Tool in Viral Transcriptome Research: Trends in Microbiology
Long-read sequencing in human genetics | SpringerLink
Haplotype-Phased Synthetic Long Reads from Short-Read Sequencing | PLOS ONE
Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses | Semantic Scholar
New study illustrates benefits of long-read sequencing technology for precision oncology | Genome Sciences Centre
Piecing together the genome: the long and short of it all – HudsonAlpha Institute for Biotechnology
Genome sequencing: Long reads for a short plant | Nature Plants
SMRT Long-Read Sequencing Solves Genetic Mysteries
Sequencing 101: the evolution of DNA sequencing tools - PacBio
Long-Read Sequencing – A Powerful Tool in Viral Transcriptome Research: Trends in Microbiology
NGS and Long-read sequencing for diagnosing short tandem repeat... | Download Scientific Diagram
![PDF] Long reads: their purpose and place | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/7ac7a62031438eea3b2cd8343147e609d4b5ea85/2-Table1-1.png "PDF] Long reads: their purpose and place | Semantic Scholar")
PDF] Long reads: their purpose and place | Semantic Scholar
Nanopore sequencing The advantages of long reads for genome assembly
Opportunities and challenges in long-read sequencing data analysis | Genome Biology | Full Text
Long-Read Sequencing – A Powerful Tool in Viral Transcriptome Research - ScienceDirect
New study illustrates benefits of long-read sequencing technology for precision oncology | Genome Sciences Centre
WGS – Macrogen
Frontiers | Long-Read Sequencing Emerging in Medical Genetics
Novel sequencing technologies and bioinformatic tools for deciphering the non-coding genome
Frontiers | Long-Read Sequencing Emerging in Medical Genetics
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma | Scientific Reports
Frontiers | Long-Read Sequencing Emerging in Medical Genetics
Figure 5 | Pharmacogenomic Biomarkers for Improved Drug Therapy—Recent Progress and Future Developments | SpringerLink
