Difference between revisions of "CopySeq"
(Created page with "{{Bioinformatics application |sw summary=CopySeq analyzes the depth-of-coverage of whole genome resequencing data to predict CNVs and to infer quantitative locus copy-number geno...") |
|||
| Line 6: | Line 6: | ||
|input format=BAM, SVF | |input format=BAM, SVF | ||
|output format=tab-delimited file | |output format=tab-delimited file | ||
| − | |language=Java 1.6 | + | |language=Java 1.6, R |
|os=Mac OS X 10.5, Linux, | |os=Mac OS X 10.5, Linux, | ||
}} | }} | ||
Revision as of 13:38, 13 April 2011
|
Application data |
|
| Biological application domain(s) | Structural variants, Copy number estimation, Genotyping, Personal genomics |
|---|---|
| Technology | Illumina/Solexa |
| Maintained? | Yes |
| Input format(s) | BAM, SVF |
| Output format(s) | tab-delimited file |
| Programming language(s) | Java 1.6, R |
| Operating system(s) | Mac OS X 10.5, Linux |
Summary: CopySeq analyzes the depth-of-coverage of whole genome resequencing data to predict CNVs and to infer quantitative locus copy-number genotypes.
"Error: no local variable "counter" was set." is not a number.
Description
Links
References
To add a reference for CopySeq, enter the PubMed ID in the field below and click 'Add'.
[ edit box ]
Search for "CopySeq" in the SEQanswers forum / BioStar or:
| Web Search | Wiki Sites | Scientific |
|---|---|---|
