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Short read alignment with populations of genomes

Summary: The increasing availability of high-throughput sequencing technologies has led to thousands of human genomes having been sequenced in the past years. Efforts such as the 1000 Genomes Project further add to the availability of human genome variation data. However, to date, there is no method...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Huang, Lin, Popic, Victoria, Batzoglou, Serafim
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2013
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3694645/
https://ncbi.nlm.nih.gov/pubmed/23813006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt215
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