Presentations

The Computational Biology Core (CBC) at Brown University (supported by the COBRE Center for Computational Biology of Human Disease) is teaming up with R/Bioconductor Staff to do two workshops...

The field of epigenetics is branching down many new and exciting avenues. One of these avenues is the area of RNA modification research. Recent advancements in the development of RNA modification detection and sequencing methods...

This RNA-seq workshop will address critical issues related to Transcriptomics data, like: Processing raw Next Generation Sequencing (NGS) data: 1. Next Generation Sequencing data preprocessing: Trimming technical sequences Removing PCR duplicates 2. RNA-seq based quantification of expression levels: Conventional pipelines ...

This Center for Evolution and Medicine Seminar features Nicholas Banovich, Assistant Professor in the Integrated Cancer Genomics Division at the Translational Genomics Research Institute...

I would like to share to the community of this RNA-Seq blog the presentation made by our company Acobiom about its MaRS database. To download this presentation, please click here: www.acobiom.com/wp-content/uploads/2016/12/mars_pracedays2017.pdf For more information, please contact Acobiom: busdev@acobiom.com  

Recent advances in single-cell RNA sequencing are producing exciting new insights into cell diversity within different tissues and cancers. Listen in to hear Dr Gonçalo Castelo-Branco and Dr Amit Zeisel, of the the Department of Medical Biochemistry...

To allow efficient transcript/gene detection, highly abundant ribosomal RNAs (rRNA) are generally removed from total RNA either by positive polyA+ selection or by rRNA depletion (negative selection)...

This Center for Evolution and Medicine Seminar features Nicholas Banovich, Assistant Professor in the Integrated Cancer Genomics Division at the Translational Genomics Research Institute.

Transcriptome Analysis using RNA-Seq Data - Short course on Statistical Genetics and Genomics - Dr Xiangquin Cui - Emory University

The Isoform Sequencing (Iso - Seq™) method employs long reads to sequence transcript isoforms from the 5’ end to their poly - A tails, eliminating the need for transcript reconstruction and inference. These long reads result in complete, unambiguous...