Genome Biology

official impact factor 6.89

Open Access Research

Finishing the finished human chromosome 22 sequence

Charlotte G Cole1, Owen T McCann1, John E Collins1, Karen Oliver1, David Willey1, Susan M Gribble1, Fengtang Yang1, Karen McLaren1, Jane Rogers1, Zemin Ning1, David M Beare1 and Ian Dunham1,2*

Author Affiliations

1 The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK

2 EMBL-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD, UK

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Genome Biology 2008, 9:R78 doi:10.1186/gb-2008-9-5-r78

Published: 13 May 2008

Additional files

Additional data file 1:

Clone libraries used in this work.

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Additional data file 2:

Coordinates of the gaps and deletions addressed in this work on numerous genome builds and the tile path file specification for chromosome 22.

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Additional data file 3:

The table and tpf file from Additional data file 1 in tab delimited text format.

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Additional data file 4:

STSs used in clone library screening as referred to in Figures S4-S13.

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Additional data file 5:

Long PCR products generated.

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Additional data file 6:

Clones identified as mapping to human chromosome 22p or 22cen.

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Additional data file 7:

Figures S1-S15.

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