| License: Creative Commons Attribution 4.0 (1MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-400963
- DOI to cite this document:
- 10.5283/epub.40096
Abstract
Background RNA sequencing (RNA-seq) has become the standard means of analyzing gene and transcript expression in high-throughput. While previously sequence alignment was a time demanding step, fast alignment methods and even more so transcript counting methods which avoid mapping and quantify gene and transcript expression by evaluating whether a read is compatible with a transcript, have led to ...

Owner only: item control page