Abstract
We present a program to improve haplotype reconstruction by incorporating information from paired-end reads, and demonstrate its utility on simulated data. We find that given a fixed coverage, longer reads (implying fewer of them) are preferable. Availability: The executable and user manual can be freely downloaded from. © 2009 The Author(s).
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CITATION STYLE
APA
Long, Q., MacArthur, D., Ning, Z., & Tyler-Smith, C. (2009). HI: Haplotype improver using paired-end short reads. Bioinformatics, 25(18), 2436–2437. https://doi.org/10.1093/bioinformatics/btp412
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