Difference between revisions of "ERDS"
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|sw summary=ERDS is a free, open-source software, designed for detection of copy number variants (CNVs) on human genomes from next generation sequence data. It uses paired Hidden Markov models (PHMM) based on the expected distribution of read depth of short reads and the presence of heterozygous sites. ERDS is NOT good for whole exome data. | |sw summary=ERDS is a free, open-source software, designed for detection of copy number variants (CNVs) on human genomes from next generation sequence data. It uses paired Hidden Markov models (PHMM) based on the expected distribution of read depth of short reads and the presence of heterozygous sites. ERDS is NOT good for whole exome data. | ||
|bio domain=Copy number estimation | |bio domain=Copy number estimation | ||
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== Description == | == Description == | ||
Latest revision as of 22:41, 19 December 2015
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Application data |
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| Biological application domain(s) | Copy number estimation |
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| Maintained? | Maybe |
Summary: ERDS is a free, open-source software, designed for detection of copy number variants (CNVs) on human genomes from next generation sequence data. It uses paired Hidden Markov models (PHMM) based on the expected distribution of read depth of short reads and the presence of heterozygous sites. ERDS is NOT good for whole exome data.
"Error: no local variable "counter" was set." is not a number.
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