MRHMMs 2 – Multivariate Regression Hidden Markov Models and the variantS

MRHMMs 2

:: DESCRIPTION

MRHMMs accommodates a variety of HMMs that can be flexibly applied to many biological studies and beyond.

::DEVELOPER

MRHMMs team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/MacOsX/ WIndows
  • C Compiler

:: DOWNLOAD

 MRHMMs

:: MORE INFORMATION

Citation:

Bioinformatics. 2014 Feb 27. [Epub ahead of print]
MRHMMs: Multivariate Regression Hidden Markov Models and the variantS.
Lee Y1, Ghosh D, Hardison RC, Zhang Y.

OpenCRAVAT 2.2.7 – Open Custom Ranked Analysis of Variants Toolkit

OpenCRAVAT 2.2.7

:: DESCRIPTION

OpenCRAVAT is a new open source, scalable decision support system to support variant and gene prioritization. It offers a dynamic GUI, allowing users to easily, download tools from an extensive resource catalog, create customized pipelines, run jobs at speeds that exceed current variant annotation API services, and explore results in a richly detailed viewing environment.

::DEVELOPER

Karchin Lab

:: SCREENSHOTS

N/A

::REQUIREMENTS

  • Windows/ Linux

:: DOWNLOAD

OpenCRAVAT

:: MORE INFORMATION

Citation

Pagel KA, Kim R, Moad K, Busby B, Zheng L, Tokheim C, Ryan M, Karchin R.
Integrated Informatics Analysis of Cancer-Related Variants.
JCO Clin Cancer Inform. 2020 Mar;4:310-317. doi: 10.1200/CCI.19.00132. PMID: 32228266; PMCID: PMC7113103.

CRAVAT: cancer-related analysis of variants toolkit.
Douville C, Carter H, Kim R, Niknafs N, Diekhans M, Stenson PD, Cooper DN, Ryan M, Karchin R.
Bioinformatics. 2013 Mar 1;29(5):647-8. doi: 10.1093/bioinformatics/btt017. Epub 2013 Jan 16.

CancerVar – Cancer Variants interpretation

CancerVar

:: DESCRIPTION

CancerVar is a bioinformatics software tool for clinical interpretation of somatic variants.

::DEVELOPER

Wang Genomics Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

CancerVar

:: MORE INFORMATION

Citation

Li Q, Ren Z, Zhou Y, Wang K.
CancerVar: a web server for improved evidence-based clinical interpretation of cancer somatic mutations and copy number abnormalities.
bioRxiv, 2020.