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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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Huang, Lin, Popic, Victoria, Batzoglou, Serafim
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Oxford University Press 2013
Θέματα:
Διαθέσιμο Online: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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