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ViralFusionSeq [VFS] download for Linux

Free download ViralFusionSeq [VFS] Linux app to run online in Ubuntu online, Fedora online or Debian online

This is the Linux app named ViralFusionSeq [VFS] whose latest release can be downloaded as vfs-2016-08-17.r2.tar.gz. It can be run online in the free hosting provider OnWorks for workstations.

Download and run online this app named ViralFusionSeq [VFS] with OnWorks for free.

Follow these instructions in order to run this app:

- 1. Downloaded this application in your PC.

- 2. Enter in our file manager https://www.onworks.net/myfiles.php?username=XXXXX with the username that you want.

- 3. Upload this application in such filemanager.

- 4. Start the OnWorks Linux online or Windows online emulator or MACOS online emulator from this website.

- 5. From the OnWorks Linux OS you have just started, goto our file manager https://www.onworks.net/myfiles.php?username=XXXXX with the username that you want.

- 6. Download the application, install it and run it.

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ViralFusionSeq [VFS]


DESCRIPTION

VFS was fullly tested under Ubuntu/Debian system.

** Announcement 1**: VFS is superior to Virus-Clip. https://sourceforge.net/projects/viralfusionseq/files/VFS.vs.Virus-Clip.pdf/download

As of 2016, VFS is the only viral integration tool available at NIH HPC system.
https://hpc.nih.gov/apps/ViralFusionSeq/

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.

Citation: http://www.ncbi.nlm.nih.gov/pubmed/

Features

  • 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


Audience

Science/Research



Programming Language

Perl



This is an application that can also be fetched from https://sourceforge.net/projects/viralfusionseq/. It has been hosted in OnWorks in order to be run online in an easiest way from one of our free Operative Systems.


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