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Showing 1 to 3 of 3 for “"Short read sequences"”.

  1. A GPU program to compute SNP-SNP interactions in genome-wide association studies

    … in the next generation sequencing technologies, short read sequences of human genome are made more accessible. Paired end sequencing of short reads is currently the most sensitive method for detecting somatic mutations that arise during tumor development. In this study, a novel approach to …

    njit Repository record for A GPU program to compute SNP-SNP interactions in genome-wide association studies (opens in a new tab)

  2. Rarity, cause or consequence: comparative landscape genomics of six lichenized fungi with contrasting range sizes, life histories, and morphologies

    … patterns associated with rarity in related widespread and range-restricted lichenized fungi sampled throughout the Appalachian Mountains of eastern North America. This research produced robust genomic datasets for widespread species (Punctelia rudecta, Lepraria finkii, and Usnea strigosa) and rare …

    eastern-wash Repository record for Rarity, cause or consequence: comparative landscape genomics of six lichenized fungi with contrasting range sizes, life histories, and morphologies (opens in a new tab)

  3. Statistical Methods For Assessing Structural Change In Human & Microbial Genomes

    … sequencing. However, due to large numbers of short read sequences, the accuracy of high-throughput sequencing data remains a challenge in that the data obtained from next-generation sequencing often has higher error rates, which may impact downstream genomic analysis. Even if the downstream …

    uthsc Repository record for Statistical Methods For Assessing Structural Change In Human & Microbial Genomes (opens in a new tab)