Rascaf – Improving Genome Assembly with RNA Sequencing Data

December 6, 2016 Leave a comment 4,271 Views

Abundant but short second-generation sequencing reads make assembly difficult, leading to fragmented genomes and gene annotations. Gene structure information from RNA sequences can be used to improve the completeness and contiguity of an assembly, but bioinformatics methods have been lacking. ...

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Rascaf – Improving Genome Assembly with RNA Sequencing Data

Associate Professor

Using single-cell RNA sequencing to disentangle the blood system

Arriba – accurate and efficient detection of gene fusions from RNA sequencing data

MSRG – new database of mosquito small RNA transcriptomes

Single-cell RNA sequencing reveals SARS-CoV-2 infection dynamics in the lungs

Genuity Science wins 2021 BIG Innovation Award for novel approach to analysis of single-cell RNA sequencing data

CLInt-Seq – a method to more efficiently isolate and identify rare T cells