PyLOH 1.4.3 – Discovering Copy Number Variations in Cancer Genomes

PyLOH 1.4.3

:: DESCRIPTION

PyLOH is a tool for discovering copy number variations in cancer genomes

::DEVELOPER

CBCL Lab (Computational Biology and Computational Learning) @ UCI

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/ Windows/MacOsX
  • Python

:: DOWNLOAD

  PyLOH

 :: MORE INFORMATION

Citation

Bioinformatics. 2014 Apr 21.
Deconvolving tumor purity and ploidy by integrating copy number alterations and loss of heterozygosity.
Li Y1, Xie X.

BaalChIP 1.12.0 – Bayesian Analysis of Allele-specific Transcription Factor Binding in Cancer Genomes

BaalChIP 1.12.0

:: DESCRIPTION

BaalChIP ( Bayesian Analysis of Allelic imbalances from ChIP-seq data) corrects for the effect of background allele frequency on the observed ChIP-seq read counts jointly analyses multiple ChIP-seq samples across a single variant.

::DEVELOPER

the Markowetz lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / MacOsX / Windows
  • R
  • BioCOnductor

:: DOWNLOAD

BaalChIP

:: MORE INFORMATION

Citation

Genome Biol, 18 (1), 39 2017 Feb 24
BaalChIP: A probabilistic framework for reconstructing intra-tumor phylogenies
I. de Santiago, W. Liu, K. Yuan, M. O’Reilly, CS. Chilamakuri, B. Ponder, K. Meyer, F. Markowetz