CNANorm

From SEQwiki
Jump to: navigation, search

Application data

Created by Stefano Berri and Arief Gusnanto
Biological application domain(s) Cancer biology, Copy number estimation, Genomics
Principal bioinformatics method(s) Peak calling, Standardisation and normalisation
Technology Illumina
Created at University of Leeds
Maintained? Yes
Input format(s) Delimited Text, SAM, BAM
Output format(s) Delimited Text
Programming language(s) R, Perl
Software libraries SAMtools
Licence GPLv2
Operating system(s) Linux, Mac OS X, Windows

Summary: A normalization method for Copy Number Aberration in cancer samples.

"Error: no local variable "counter" was set." is not a number.

Description

Performs ratio, GC content correction and normalization of data obtained using low coverage (one read every 100-10,000 bp) high throughput sequencing. It performs a "discrete" normalization looking for the ploidy of the genome. It will also provide tumour content if at least two ploidy states can be found.



Links


References

  1. . 2011. Bioinformatics


To add a reference for CNANorm, enter the PubMed ID in the field below and click 'Add'.

 


Search for "CNANorm" in the SEQanswers forum / BioStar or:

Web Search Wiki Sites Scientific