Publications by authors named "Annie Lui"

The domestic dog, Canis familiaris, is a well-established model system for mapping trait and disease loci. While the original draft sequence was of good quality, gaps were abundant particularly in promoter regions of the genome, negatively impacting the annotation and study of candidate genes. Here, we present an improved genome build, canFam3.

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We have sequenced the genomes of 18 isolates of the closely related human pathogenic fungi Coccidioides immitis and Coccidioides posadasii to more clearly elucidate population genomic structure, bringing the total number of sequenced genomes for each species to 10. Our data confirm earlier microsatellite-based findings that these species are genetically differentiated, but our population genomics approach reveals that hybridization and genetic introgression have recently occurred between the two species. The directionality of introgression is primarily from C.

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Comparative analysis of multiple genomes in a phylogenetic framework dramatically improves the precision and sensitivity of evolutionary inference, producing more robust results than single-genome analyses can provide. The genomes of 12 Drosophila species, ten of which are presented here for the first time (sechellia, simulans, yakuba, erecta, ananassae, persimilis, willistoni, mojavensis, virilis and grimshawi), illustrate how rates and patterns of sequence divergence across taxa can illuminate evolutionary processes on a genomic scale. These genome sequences augment the formidable genetic tools that have made Drosophila melanogaster a pre-eminent model for animal genetics, and will further catalyse fundamental research on mechanisms of development, cell biology, genetics, disease, neurobiology, behaviour, physiology and evolution.

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Chromosome 17 is unusual among the human chromosomes in many respects. It is the largest human autosome with orthology to only a single mouse chromosome, mapping entirely to the distal half of mouse chromosome 11. Chromosome 17 is rich in protein-coding genes, having the second highest gene density in the genome.

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Article Synopsis
  • The study presents a complete sequence of human chromosome 15, accompanied by a detailed gene catalogue.
  • Chromosome 15 is characterized by high rates of segmental duplication, particularly in two areas which are important for understanding genetic disorders like Prader-Willi and Angelman syndromes.
  • The researchers identified that most duplications have a common ancestry and that gaps in the genome sequence may arise from structural differences between genetic variants, contributing to ongoing challenges in mapping the human genome.
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Article Synopsis
  • - A high-quality draft genome sequence of the domestic dog has been completed, revealing its evolutionary significance and the diverse traits among various breeds.
  • - The research includes a detailed map of single nucleotide polymorphisms (SNPs), which helps understand genetic diversity within and among dog breeds.
  • - This SNP map facilitates genome-wide association studies that can identify genes linked to diseases and traits, benefiting both human and canine health.
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Chromosome 18 appears to have the lowest gene density of any human chromosome and is one of only three chromosomes for which trisomic individuals survive to term. There are also a number of genetic disorders stemming from chromosome 18 trisomy and aneuploidy. Here we report the finished sequence and gene annotation of human chromosome 18, which will allow a better understanding of the normal and disease biology of this chromosome.

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