Transcriptome Sequencing: RNA-Seq
Transcriptome Sequencing: RNA-Seq
RNA sequencing (RNA-seq) can not only be used to identify the expression of common or rare transcripts but also in the identification of other abnormal events, such as alternative splicing, novel transcripts, and fusion genes. In principle, RNA-seq can be carried out by almost all of the next-generation sequencing (NGS) platforms, but the libraries of different platforms are not exactly the same; each platform has its own kit to meet the special requirements of the instrument design.
- Shanghai Jiao Tong University China (People's Republic of)
Data Analysis, Alternative Splicing, Base Sequence, Sequence Analysis, RNA, Gene Expression Profiling, High-Throughput Nucleotide Sequencing, RNA, Gene Fusion, Transcriptome
Data Analysis, Alternative Splicing, Base Sequence, Sequence Analysis, RNA, Gene Expression Profiling, High-Throughput Nucleotide Sequencing, RNA, Gene Fusion, Transcriptome
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).79 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 1% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
Citations provided by BIP!Popularity provided by BIP!