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Closing gaps in the human genome using sequencing by synthesis.
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Schanzer, Andres
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Closing gaps in the human genome using sequencing by synthesis.
Garber M, Zody MC, Arachchi HM, Berlin A, Gnerre S, Green LM, Lennon N, Nusbaum C. Closing gaps in the human genome using sequencing by synthesis. Genome Biol. 2009; 10(6):R60.
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PubMed
subject areas
Base Sequence
Cell Line
Chromosomes, Human, Pair 15
Genome, Human
Humans
Sequence Analysis, DNA
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Manuel Garber PhD