دورية أكاديمية

Long Interspersed Element Sequencing (L1-Seq): A Method to Identify Somatic LINE-1 Insertions in the Human Genome.

التفاصيل البيبلوغرافية
العنوان: Long Interspersed Element Sequencing (L1-Seq): A Method to Identify Somatic LINE-1 Insertions in the Human Genome.
المؤلفون: Doucet TT; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA., Kazazian HH Jr; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA. kazazian@jhmi.edu.; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. kazazian@jhmi.edu.
المصدر: Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2016; Vol. 1400, pp. 79-93.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Humana Press Country of Publication: United States NLM ID: 9214969 Publication Model: Print Cited Medium: Internet ISSN: 1940-6029 (Electronic) Linking ISSN: 10643745 NLM ISO Abbreviation: Methods Mol Biol Subsets: MEDLINE
أسماء مطبوعة: Publication: Totowa, NJ : Humana Press
Original Publication: Clifton, N.J. : Humana Press,
مواضيع طبية MeSH: Genome, Human* , Genomics*/methods , Long Interspersed Nucleotide Elements*, Computational Biology/methods ; Genomic Library ; High-Throughput Nucleotide Sequencing ; Humans ; Reproducibility of Results
مستخلص: L1-seq is a high-throughput sequencing technique which is utilized to identify novel L1 insertions in genomic DNA samples of interest. Using special diagnostic nucleotides unique to the youngest and most active L1 sequence, we can amplify new somatic insertions. This technique has helped to establish the number of L1 insertions present in the general population as well as the variation among individuals with regard to their complement of active L1 elements. More recently, this technique has been employed to assess the level of retrotransposition occurring in various diseases such as cancer. These efforts try to establish a connection between the process of retrotransposition and disease development and/or progression.
References: Nat Genet. 2003 Sep;35(1):41-8. (PMID: 12897783)
Nat Genet. 2000 Apr;24(4):363-7. (PMID: 10742098)
Genome Res. 2014 Jul;24(7):1053-63. (PMID: 24823667)
Cell. 2013 Mar 28;153(1):101-11. (PMID: 23540693)
Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7124-8. (PMID: 1379734)
Nucleic Acids Res. 2015 Jan;43(Database issue):D43-7. (PMID: 25352549)
Proc Natl Acad Sci U S A. 2015 Sep 1;112(35):E4894-900. (PMID: 26283398)
Curr Opin Genet Dev. 2012 Jun;22(3):191-203. (PMID: 22406018)
Am J Hum Genet. 2003 Dec;73(6):1444-51. (PMID: 14628287)
Science. 2012 Aug 24;337(6097):967-71. (PMID: 22745252)
Science. 2014 Aug 1;345(6196):1251343. (PMID: 25082706)
Nature. 2011 Oct 30;479(7374):534-7. (PMID: 22037309)
Genome Res. 2012 Dec;22(12):2328-38. (PMID: 22968929)
Genome Res. 2010 Sep;20(9):1262-70. (PMID: 20488934)
Cell. 2012 Oct 26;151(3):483-96. (PMID: 23101622)
معلومات مُعتمدة: R01 GM099875 United States GM NIGMS NIH HHS
فهرسة مساهمة: Keywords: L1; LINE-1; Next-Generation DNA sequencing; Non-LTR retrotransposon; Retroelement
تواريخ الأحداث: Date Created: 20160220 Date Completed: 20161213 Latest Revision: 20220408
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC5340310
DOI: 10.1007/978-1-4939-3372-3_5
PMID: 26895047
قاعدة البيانات: MEDLINE
الوصف
تدمد:1940-6029
DOI:10.1007/978-1-4939-3372-3_5