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Christine Lloyd

Researcher at Wellcome Trust Sanger Institute

Publications -  17
Citations -  33630

Christine Lloyd is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Genome & Human genome. The author has an hindex of 14, co-authored 17 publications receiving 31837 citations. Previous affiliations of Christine Lloyd include Wellcome Trust.

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Journal ArticleDOI

Initial sequencing and analysis of the human genome.

Eric S. Lander, +248 more
- 15 Feb 2001 - 
TL;DR: The results of an international collaboration to produce and make freely available a draft sequence of the human genome are reported and an initial analysis is presented, describing some of the insights that can be gleaned from the sequence.
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Initial sequencing and comparative analysis of the mouse genome.

Robert H. Waterston, +222 more
- 05 Dec 2002 - 
TL;DR: The results of an international collaboration to produce a high-quality draft sequence of the mouse genome are reported and an initial comparative analysis of the Mouse and human genomes is presented, describing some of the insights that can be gleaned from the two sequences.
Journal ArticleDOI

The DNA sequence of the human X chromosome

Mark T. Ross, +282 more
- 17 Mar 2005 - 
TL;DR: This analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome.
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The DNA sequence of human chromosome 22

Ian Dunham, +223 more
- 02 Dec 1999 - 
TL;DR: The sequence of the euchromatic part of human chromosome 22 is reported, which consists of 12 contiguous segments spanning 33.4 megabases, contains at least 545 genes and 134 pseudogenes, and provides the first view of the complex chromosomal landscapes that will be found in the rest of the genome.
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DNA sequence and analysis of human chromosome 9

Andrew J. Mungall, +170 more
- 23 Oct 2003 - 
TL;DR: Analysis of the sequence reveals many intra- and interchromosomal duplications, including segmental duplications adjacent to both the centromere and the large heterochromatic block, and detects recently duplicated genes that exhibit different rates of sequence divergence, presumably reflecting natural selection.