{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T12:09:56Z","timestamp":1762430996966},"reference-count":19,"publisher":"Oxford University Press (OUP)","issue":"19","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Summary: There are several experimental contexts in which it is important to identify DNA integration sites, such as insertional mutagenesis screens, gene and enhancer trap applications, and gene therapy. We previously developed an assay to identify millions of integrations in multiplexed barcoded samples at base-pair resolution. The sheer amount of data produced by this approach makes the mapping of individual sites non-trivial without bioinformatics support. This article presents the Genomic Integration Site Tracker (GeIST), a command-line pipeline designed to map the integration sites produced by this assay and identify the samples from which they came. GeIST version 2.1.0, a more adaptable version of our original pipeline, can identify integrations of murine leukemia virus, adeno-associated virus, Tol2 transposons or Ac\/Ds transposons, and can be adapted for other inserted elements. It has been tested on experimental data for each of these delivery vectors and fine-tuned to account for sequencing and cloning artifacts.<\/jats:p>\n               <jats:p>Availability and implementation: GeIST uses a combination of Bash shell scripting and Perl. GeIST is available at http:\/\/research.nhgri.nih.gov\/software\/GeIST\/.<\/jats:p>\n               <jats:p>Contact: \u00a0burgess@mail.nih.gov<\/jats:p>","DOI":"10.1093\/bioinformatics\/btv350","type":"journal-article","created":{"date-parts":[[2015,6,7]],"date-time":"2015-06-07T00:01:38Z","timestamp":1433635298000},"page":"3219-3221","source":"Crossref","is-referenced-by-count":6,"title":["GeIST: a pipeline for mapping integrated DNA elements"],"prefix":"10.1093","volume":"31","author":[{"given":"Matthew C.","family":"LaFave","sequence":"first","affiliation":[{"name":"Translational and Functional Genomics Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-8004, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gaurav K.","family":"Varshney","sequence":"additional","affiliation":[{"name":"Translational and Functional Genomics Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-8004, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shawn M.","family":"Burgess","sequence":"additional","affiliation":[{"name":"Translational and Functional Genomics Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-8004, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2015,6,6]]},"reference":[{"key":"2023020202304224000_btv350-B1","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1038\/ng.2847","article-title":"Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model","volume":"46","author":"Bard-Chapeau","year":"2014","journal-title":"Nat. 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