# PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/penncnv-an-integrated-hidden-markov-model-designed-for-high-resolution-copy/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Kai Wang,Mingyao Li,Dexter Hadley,Rui Liu,Joseph Glessner,Struan F.A. Grant,Håkon Håkonarson,Maja Bućan |
| Citations | 1,914 |
| DOI | 10.1101/gr.6861907 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://genome.cshlp.org/content/17/11/1665.full.pdf |
| OpenAlex ID | https://openalex.org/W2149681218 |
| PMID | 17921354 |
| Type | preprint |
| Year | 2007 |

## Paper authors

- [Kai Wang](https://scholariq.org/researchers/kai-wang-2/)

## Paper primary topic

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Paper topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Gene expression and cancer classification](https://scholariq.org/topics/gene-expression-and-cancer-classification/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.