Article
Short read alignment with populations of genomes.
Bioinformatics (Oxford, England) - 1 Jul 2013
Huang Lin, Popic Victoria, Batzoglou Serafim
Abstract excerpt
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 that can map reads of a newly sequenced human genome to a large collection of genomes. Instead, methods rely on...
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