** Announcement 1 **: VFS is officially described in Bioinformatics
** Announcement 2 **: 1 minute crash course of VFS now available in sourceforge's "Wiki" section
** Announcement 3 **: Any immediate concern about Installation issue(s) / question(s) should be addressed to email@example.com
ViralFusionSeq (VFS) is a versatile high-throughput sequencing (HTS) tool for discovering viral integration events and reconstruct fusion transcripts at single-base resolution.
VFS combines soft-clipping information, read-pair analysis, and targeted de novo assembly to discover and annotate viral-human fusion events.
A simple yet effective empirical statistical model is used to evaluate the quality of fusion breakpoints.
Minimal user defined parameters are required.
Source code with user manual and installation guide of VFS is available at sourceforge's "Files" section.
For indexing purpose: Viral Fusion Seq
- Applicable and fully tested using RNA-Seq and DNA-Seq data
- Utilize both clipped-sequence (CS) and paired-end (RP) information to discover viral integration
- Re-construction of fusion transcript sequence using CS and RP information
Viralfusionseq works great.
Simple to use.