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R Ainscough

Researcher at Wellcome Trust Sanger Institute

Publications -  10
Citations -  26091

R Ainscough is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Human genome & Chromosome 19. The author has an hindex of 10, co-authored 10 publications receiving 24688 citations. Previous affiliations of R Ainscough 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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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.
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The DNA sequence and comparative analysis of human chromosome 20.

Panos Deloukas, +135 more
- 27 May 2004 - 
TL;DR: Comparative analysis of the sequence of chromosome 20 to whole-genome shotgun-sequence data of two other vertebrates provides an independent measure of the efficiency of gene annotation, and indicates that this analysis may account for more than 95% of all coding exons and almost all genes.