Literature DB >> 17138589

Visualization of genomic aberrations using Affymetrix SNP arrays.

André Müller1, Karlheinz Holzmann, Hans A Kestler.   

Abstract

MOTIVATION: DNA copy number aberrations are frequently found in different types of cancer. Recent developments of microarray-based approaches have broadened the knowledge on number and structure of such aberrations. High-density single nucleotide polymorphism (SNP) microarrays provide an extremely high resolution with up to 500,000 SNPs per genome. Owing to the enormous amount of data the detection of common aberrations in large datasets is a great challenge. We describe a novel open source software tool--IdeogramBrowser--which was specifically designed for use with the Affymetrix SNP arrays. It provides an interactive karyotypic visualization of multiple aberration profiles and direct links to GeneCards. Visualization of consensus regions together with gene representation allows the explorative assessment of the data. AVAILABILITY: IdeogramBrowser and its source code are freely available under a creative commons license and can be obtained from http://www.informatik.uni-ulm.de/ni/staff/HKestler/ideo/. IdeogramBrowser is a platform independent Java application.

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Year:  2006        PMID: 17138589     DOI: 10.1093/bioinformatics/btl608

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  12 in total

1.  Identification of germline genomic copy number variation in familial pancreatic cancer.

Authors:  Wigdan Al-Sukhni; Sarah Joe; Anath C Lionel; Nora Zwingerman; George Zogopoulos; Christian R Marshall; Ayelet Borgida; Spring Holter; Aaron Gropper; Sara Moore; Melissa Bondy; Alison P Klein; Gloria M Petersen; Kari G Rabe; Ann G Schwartz; Sapna Syngal; Stephen W Scherer; Steven Gallinger
Journal:  Hum Genet       Date:  2012-06-05       Impact factor: 4.132

2.  Pan-colonic field defects are detected by CGH in the colons of UC patients with dysplasia/cancer.

Authors:  Lisa A Lai; Rosa Ana Risques; Mary P Bronner; Peter S Rabinovitch; David Crispin; Ru Chen; Teresa A Brentnall
Journal:  Cancer Lett       Date:  2012-03-02       Impact factor: 8.679

3.  3D Network exploration and visualisation for lifespan data.

Authors:  Rolf Hühne; Viktor Kessler; Axel Fürstberger; Silke Kühlwein; Matthias Platzer; Jürgen Sühnel; Ludwig Lausser; Hans A Kestler
Journal:  BMC Bioinformatics       Date:  2018-10-23       Impact factor: 3.169

4.  Upregulation of FOXM1 induces genomic instability in human epidermal keratinocytes.

Authors:  Muy-Teck Teh; Emilios Gemenetzidis; Tracy Chaplin; Bryan D Young; Michael P Philpott
Journal:  Mol Cancer       Date:  2010-02-26       Impact factor: 27.401

5.  Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2.

Authors:  Ulrich Pannicke; Manfred Hönig; Isabell Hess; Claudia Friesen; Karlheinz Holzmann; Eva-Maria Rump; Thomas F Barth; Markus T Rojewski; Ansgar Schulz; Thomas Boehm; Wilhelm Friedrich; Klaus Schwarz
Journal:  Nat Genet       Date:  2008-11-30       Impact factor: 38.330

6.  Currents in contemporary bioethics. Identifying consanguinity through routine genomic analysis: reporting requirements.

Authors:  Amy L McGuire; Melody J Wang; Frank J Probst
Journal:  J Law Med Ethics       Date:  2012       Impact factor: 1.718

7.  In-silico human genomics with GeneCards.

Authors:  Gil Stelzer; Irina Dalah; Tsippi Iny Stein; Yigeal Satanower; Naomi Rosen; Noam Nativ; Danit Oz-Levi; Tsviya Olender; Frida Belinky; Iris Bahir; Hagit Krug; Paul Perco; Bernd Mayer; Eugene Kolker; Marilyn Safran; Doron Lancet
Journal:  Hum Genomics       Date:  2011-10       Impact factor: 4.639

8.  Olorin: combining gene flow with exome sequencing in large family studies of complex disease.

Authors:  James A Morris; Jeffrey C Barrett
Journal:  Bioinformatics       Date:  2012-10-10       Impact factor: 6.937

9.  FISH Oracle: a web server for flexible visualization of DNA copy number data in a genomic context.

Authors:  Malte Mader; Ronald Simon; Sascha Steinbiss; Stefan Kurtz
Journal:  J Clin Bioinforma       Date:  2011-07-28

10.  Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.

Authors:  Jian Li; Tielin Yang; Liang Wang; Han Yan; Yinping Zhang; Yan Guo; Feng Pan; Zhixin Zhang; Yumei Peng; Qi Zhou; Lina He; Xuezhen Zhu; Hongyi Deng; Shawn Levy; Christopher J Papasian; Betty M Drees; James J Hamilton; Robert R Recker; Jing Cheng; Hong-Wen Deng
Journal:  PLoS One       Date:  2009-11-23       Impact factor: 3.240

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