The ability to study transcript isoforms in detail could have a significant impact on our understanding of health and disease. However, most commonly, bulk sequencing is the selected method that only ...
OXFORD, England--(BUSINESS WIRE)--Oxford Nanopore Technologies plc (Oxford Nanopore) today announces a collaboration with 10x Genomics, to enable a streamlined workflow for sequencing full-length ...
The analysis of genomic and transcriptomic heterogeneity at the single-cell level has provided new insights into many research areas, including cancer research, cell biology, embryonic development and ...
Long-read platforms that can sequence RNA molecules over 10,000 bases in length end-to-end hold great potential for use in characterizing variations in the transcriptome. But while these technologies ...
Transcript isoforms play a vital role in heath and disease, but studying them has been challenging due to limitations in traditional methods. By combining long nanopore sequencing reads with ...
Different variants of a gene, known as isoforms, can be transcribed and translated at varying levels within a cell or tissue. These isoforms are commonly a result of alternative splicing, which ...
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