RNA sequencing: the teenage years
By Rory Stark, Marta Grzelak, J. Hadfield. Nature reviews genetics, 2019
1,522 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/3109393967ed9e1b3c5a2e994728d0465ef07995
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Alicia Oshlack
- Michael I. Love
- W. Tam
- Gordon K. Smyth
- Aaron T. L. Lun
- Yunshun Chen
- Mark D. Robinson
- John C. Marioni
In Molecular Biology
Citations in the corpus
- PyDESeq2: a python package for bulk RNA-seq differential expression analysis (2022, methodology): “Most RNA-seq datasets are used primarily for di ↵ erential expression analysis (DEA) (Stark et al. , 2019) which provides invaluable insight on the associations between the genes’ expression and a phenotype.”
- Improved transcriptome assembly using a hybrid of long and short reads with StringTie (2021, background): “These include the rapid rate of RNA degradation, shearing of the RNA during library preparation, or incomplete synthesis of cDNA [3].”
- Next-Generation Sequencing Technology: Current Trends and Advancements (2023, methodology): “The various bioinformatics tools used in NGS analysis are listed in Table 3.”
- A systematic benchmark of Nanopore long read RNA sequencing for transcript level analysis in human cell lines (2021, background): “(8) Detection and quantification of full length fusion transcripts The occurrence of genomic rearrangements in cancer can introduce fusion genes which are associated with clinical characteristics 30.”