Chi8 v1 – GPU program for Detecting Significant Interacting SNPs with the Chi-square 8-df test

Chi8 v1

:: DESCRIPTION

Chi8 is a program that calculates the chi-square 8 degree of freedom test between all pairs of SNPs in a brute force manner on a Graphics Processing Unit.
Usman Roshan

::DEVELOPER

Usman Roshan

:: SCREENSHOTS

n/a

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 Chi8

:: MORE INFORMATION

Citation

Chi8: a GPU program for detecting significant interacting SNPs with the Chi-square 8-df test.
Al-Jouie A, Esfandiari M, Ramakrishnan S, Roshan U.
BMC Res Notes. 2015 Sep 14;8:436. doi: 10.1186/s13104-015-1392-5.

SiGPAT 0.1 – Finding significant Expression Patterns of Gene Set

SiGPAT 0.1

:: DESCRIPTION

SiGPAT is a useful tool based on gene set analysis for microarray data. It can find significant expression patterns of gene sets by pri-defined biological knowledge. To be unique to other tools, SiGPAT assignes two statistics for each gene sets and classifies expression patterns of gene sets form two dimension distribution of set-level statistics. The tool was evaluated with better performance than current tools such as GSEA and SAM-GS

::DEVELOPER

Zuguang Gu

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Windows/Linux/MacOsX
  • R package

:: DOWNLOAD

  SiGPAT

:: MORE INFORMATION

LAMPLINK v1.12 – Detection of Statistically Significant Epistatic Interactions

LAMPLINK v1.12

:: DESCRIPTION

The LAMPLINK can detect statistically significant epistatic interactions of two or more SNPs from GWAS data. This software can be used in the same way as the widely used GWAS analysis software PLINK, but LAMPLINK has the additional options for the detection of epistatic interactions with LAMP, which is a multiple testing procedure for combinatorial effects discovery. You can apply LAMPLINK to an analysis pipeline with PLINK simply by replacing plink with lamplink and adding the –lamp option.

::DEVELOPER

LAMPLINK team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • Python
  • C++ Compiler

:: DOWNLOAD

  LAMPLINK

:: MORE INFORMATION

Citation

LAMPLINK: detection of statistically significant SNP combinations from GWAS data.
Terada A, Yamada R, Tsuda K, Sese J.
Bioinformatics. 2016 Jul 13. pii: btw418.

MultiMotif – Finding Statistically Significant labeled Motifs in multi-relational networks

MultiMotif

:: DESCRIPTION

MultiMotif is a tool for finding statistically significant labeled motifs in multi-relational networks with analytically derived p-values. MultiMotif uses a custom version of RI algorithm for counting occurrences of labeled motifs in a graph and implements an analytical model to assess motifs significance without generating random graphs. MultiMotif works on both directed and undirected networks and handle non-induced labeled motifs.

::DEVELOPER

MultiMotif team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / Windows
  • Java

:: DOWNLOAD

MultiMotif

:: MORE INFORMATION

Citation:

Micale G, Pulvirenti A, Ferro A, Giugno R, Shasha D (2019).
Fast methods for finding significant motifs on labelled multi-relational networks.
Journal of Complex Networks, doi:10.1093/comnet/cnz008

LFM-Pro – Detection of Significant Local Structural Sites in Proteins

LFM-Pro

:: DESCRIPTION

LFM-Pro (Local Feature Mining in Proteins) is a framework for automatically discovering family specific local sites and the features associated with these sites.

::DEVELOPER

Sacan Bioinformatics Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Windows/Linux
  • Matlab

:: DOWNLOAD

 LFM-Pro

:: MORE INFORMATION

Citation

Ahmet Sacan, Ozgur Ozturk, Hakan Ferhatosmanoglu, and Yusu Wang.
LFM-Pro: A Tool for Detecting Significant Local Structural Sites in Proteins.
Bioinformatics, 23(6):709-716, 2007

MutSig Beta – Detect Significantly Mutated Genes

MutSig Beta

:: DESCRIPTION

MutSig (for “Mutation Significance”) is a package of tools for analyzing mutation data.  It operates on a cohort of patients and identifies mutations, genes, and other genomic elements predicted to be driver candidates.  MutSig was developed for the use case of somatic mutations, i.e. mutations that occurred during the development of cancer, and this documentation uses language specific to somatic mutations.  However, MutSig has also been used for analysis of germline mutations and is completely applicable to that use case also.

::DEVELOPER

The Cancer Genome Analysis (CGA) group

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 MutSig

:: MORE INFORMATION

Citation

Shantanu Banerji,et al.
Sequence analysis of mutations and translocations across breast cancer subtypes
Nature 486, 405–409 (21 June 2012) doi:10.1038/nature11154

SAIC – Identify Significant Consensus Aberrations in Cancer Genome

SAIC

:: DESCRIPTION

SAIC (Significant Aberrations in Cancer) is a software to identify significant consensus aberrations in cancer genome.

::DEVELOPER

Computational Bioinformatics & Bio-imaging Laboratory (CBIL)

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Windows / Linux / MacOsX
  • C Compiler

:: DOWNLOAD

 SAIC

:: MORE INFORMATION