<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ryder E</submitter><funding>Medical Research Council</funding><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>615-29</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2013729</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>177(1)</volume><pubmed_abstract>We describe a second-generation deficiency kit for Drosophila melanogaster composed of molecularly mapped deletions on an isogenic background, covering approximately 77% of the Release 5.1 genome. Using a previously reported collection of FRT-bearing P-element insertions, we have generated 655 new deletions and verified a set of 209 deletion-bearing fly stocks. In addition to deletions, we demonstrate how the P elements may also be used to generate a set of custom inversions and duplications, particularly useful for balancing difficult regions of the genome carrying haplo-insufficient loci. We describe a simple computational resource that facilitates selection of appropriate elements for generating custom deletions. Finally, we provide a computational resource that facilitates selection of</pubmed_abstract><journal>Genetics</journal><pubmed_title>The DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource.</pubmed_title><pmcid>PMC2013729</pmcid><funding_grant_id>G8225539</funding_grant_id><funding_grant_id>G18877</funding_grant_id><pubmed_authors>Nickel C</pubmed_authors><pubmed_authors>Stocker H</pubmed_authors><pubmed_authors>Ryder E</pubmed_authors><pubmed_authors>Chan YS</pubmed_authors><pubmed_authors>Marhold J</pubmed_authors><pubmed_authors>Szidonya J</pubmed_authors><pubmed_authors>Bautista-Llacer R</pubmed_authors><pubmed_authors>Maroy P</pubmed_authors><pubmed_authors>Serras F</pubmed_authors><pubmed_authors>Morley T</pubmed_authors><pubmed_authors>Ekstrom K</pubmed_authors><pubmed_authors>Johnson G</pubmed_authors><pubmed_authors>Dorner C</pubmed_authors><pubmed_authors>Kube M</pubmed_authors><pubmed_authors>Kauk A</pubmed_authors><pubmed_authors>Webster J</pubmed_authors><pubmed_authors>Schenkel H</pubmed_authors><pubmed_authors>Hafen E</pubmed_authors><pubmed_authors>Reuter G</pubmed_authors><pubmed_authors>Punset A</pubmed_authors><pubmed_authors>Coulson D</pubmed_authors><pubmed_authors>Pflugfelder G</pubmed_authors><pubmed_authors>Klimm M</pubmed_authors><pubmed_authors>Baisch H</pubmed_authors><pubmed_authors>Hugentobler C</pubmed_authors><pubmed_authors>Mechler B</pubmed_authors><pubmed_authors>Ashburner M</pubmed_authors><pubmed_authors>Rasmuson-Lestander A</pubmed_authors><pubmed_authors>Drummond J</pubmed_authors><pubmed_authors>Apelt C</pubmed_authors><pubmed_authors>Gubb D</pubmed_authors><pubmed_authors>Russell S</pubmed_authors><pubmed_authors>Corominas M</pubmed_authors><pubmed_authors>Roote J</pubmed_authors><pubmed_authors>Blows F</pubmed_authors><pubmed_authors>Pal M</pubmed_authors><pubmed_authors>Rudolph T</pubmed_authors></additional><is_claimable>false</is_claimable><name>The DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource.</name><description>We describe a second-generation deficiency kit for Drosophila melanogaster composed of molecularly mapped deletions on an isogenic background, covering approximately 77% of the Release 5.1 genome. Using a previously reported collection of FRT-bearing P-element insertions, we have generated 655 new deletions and verified a set of 209 deletion-bearing fly stocks. In addition to deletions, we demonstrate how the P elements may also be used to generate a set of custom inversions and duplications, particularly useful for balancing difficult regions of the genome carrying haplo-insufficient loci. We describe a simple computational resource that facilitates selection of appropriate elements for generating custom deletions. Finally, we provide a computational resource that facilitates selection of</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Sep</publication><modification>2025-04-05T08:50:24.227Z</modification><creation>2019-03-27T02:21:40Z</creation></dates><accession>S-EPMC2013729</accession><cross_references><pubmed>17720900</pubmed><doi>10.1534/genetics.107.076216</doi></cross_references></HashMap>