PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data

Personal-genomics endeavors, such as the 1000 Genomes project, are generating maps of genomic structural variants by analyzing ends of massively sequenced genome fragments. To process these we developed Paired-End Mapper (PEMer; ). This comprises an analysis pipeline, compatible with several next-ge...

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Detalles Bibliográficos
Autores principales: Korbel, Jan O, Abyzov, Alexej, Mu, Xinmeng Jasmine, Carriero, Nicholas, Cayting, Philip, Zhang, Zhengdong, Snyder, Michael, Gerstein, Mark B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688268/
https://www.ncbi.nlm.nih.gov/pubmed/19236709
http://dx.doi.org/10.1186/gb-2009-10-2-r23

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