bibliographic entry 8003969 [be/8003969]
https://w3id.org/oc/corpus/be/8003969

is a

• bibliographic reference

content

• Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, et al (2007) PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 17: 1665–1674. PMID: 17921354

references

• https://w3id.org/oc/corpus/br/228849