Commit 5bb34689 authored by Amonida Zadissa's avatar Amonida Zadissa
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Added description for 'Encode Duke excluded regions'.

parent 8377fc74
......@@ -5,3 +5,4 @@ Tilepath BAC clones upon which the current genomic assembly was based. Colours
1Mb clone set Clones were selected at approximately 1MB intervals in the genome to help identify breakpoints of chromosomal rearrangements. Fluorescence in situ hybridisation (FISH) mapped clones are marked by a black triangle in the upper left corner. Gold clones are also in the tilepath.
32k clone set Clones were re-arrayed by and available at <a rel="external" href="http://bacpac.chori.org/pHumanMinSet.htm">CHORI</a>. Fluorescence in situ hybridisation (FISH) mapped clones are marked by a black triangle in the upper left corner. Gold clones are also in the tilepath.
30k clone set Clone positions were determined by a Wellcome Trust Sanger Institute <a rel="external" href="https://decipher.sanger.ac.uk/perl/application?action=arraytypes;array_id=20">internal project</a>.
Encode Duke excluded regions Encode Duke excluded regions | Genomic regions that have been problematic for short sequence tag signal detection (such as satellites and rRNA genes). These regions were generated at Duke University's <a rel="external" href="http://www.genome.duke.edu/index.php">Institute for Genome Sciences & Policy (IGSP)</a> and <a rel="external" href="http://www.ebi.ac.uk/">European Bioinformatics Insitute (EBI)</a>.
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