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Tracey Honan

Researcher at Broad Institute

Publications -  5
Citations -  6601

Tracey Honan is an academic researcher from Broad Institute. The author has contributed to research in topics: Genome & Molecular evolution. The author has an hindex of 5, co-authored 5 publications receiving 6215 citations.

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Genome sequence, comparative analysis and haplotype structure of the domestic dog

Kerstin Lindblad-Toh, +241 more
- 08 Dec 2005 - 
TL;DR: A high-quality draft genome sequence of the domestic dog is reported, together with a dense map of single nucleotide polymorphisms (SNPs) across breeds, to shed light on the structure and evolution of genomes and genes.
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Evolution of genes and genomes on the Drosophila phylogeny.

Andrew G. Clark, +429 more
- 08 Nov 2007 - 
TL;DR: 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 Conformation Capture Carbon Copy (5C): A massively parallel solution for mapping interactions between genomic elements

TL;DR: A high-throughput 3C approach, 3C-Carbon Copy (5C), that employs microarrays or quantitative DNA sequencing using 454-technology as detection methods that should be widely applicable for large-scale mapping of cis- and trans- interaction networks of genomic elements and for the study of higher-order chromosome structure.
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Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences

Tarjei S. Mikkelsen, +238 more
- 10 May 2007 - 
TL;DR: A high-quality draft of the genome sequence of the grey, short-tailed opossum is reported, indicating a strong influence of biased gene conversion on nucleotide sequence composition, and a relationship between chromosomal characteristics and X chromosome inactivation.
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High-resolution description of antibody heavy-chain repertoires in humans

TL;DR: Deep sequencing is used to characterize the diversity of the heavy-chain CDR3 region, the most important contributor to antibody binding specificity, and the constituent V, D, and J segments that comprise it and finds that, during the stepwise D-J and then V-DJ recombination events, the choice of D andJ segments exert some bias on each other; however, it is found that the V segment is essentially independent of both.