by Geraldine_VdAuwera at GATK Best Practices workflow for RNAseq This workflow is intended to be run per-sample; joint calling on RNAseq is not supported yet, though that is on our roadmap. Please see the new document here for full details ...
Read More »-
AssociVar – detecting mutations based on associations from direct RNA sequencing data
One of the key challenges in the field of genetics is the inference of haplotypes from next generati...
-
Cell lineage inference from SNP and scRNA-Seq data
Several recent studies focus on the inference of developmental and response trajectories from single...
-
VaDiR – an integrated approach to variant detection in RNA
Advances in next-generation DNA sequencing technologies are now enabling detailed characterization o...
-
GROM – lightning-fast genome variant detection
Current human whole genome sequencing projects produce massive amounts of data, often creating signi...
-
Halvade-RNA – a parallel, multi-node RNA-seq variant calling pipeline based on the GATK Best Practices recommendations
Given the current cost-effectiveness of next-generation sequencing, the amount of DNA-seq and RNA-se...