Literature DB >> 23589652

UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays.

Christopher Schroeder1, Marc Sturm, Andreas Dufke, Ulrike Mau-Holzmann, Thomas Eggermann, Sven Poths, Olaf Riess, Michael Bonin.   

Abstract

UNLABELLED: UPDtool is a computational tool for detection and classification of uniparental disomy (UPD) in trio SNP-microarray experiments. UPDs are rare events of chromosomal malsegregation and describe the condition of two homologous chromosomes or homologous chromosomal segments that were inherited from one parent. The occurrence of UPD can be of major clinical relevance. Though high-throughput molecular screening techniques are widely used, detection of UPDs and especially the subclassification remains complex. We developed UPDtool to detect and classify UPDs from SNP microarray data of parent-child trios. The algorithm was tested using five positive controls including both iso- and heterodisomic segmental UPDs and 30 trios from the HapMap project as negative controls. With UPDtool, we were able to correctly identify all occurrences of non-mosaic UPD within our positive controls, whereas no occurrence of UPD was found within our negative controls. In addition, the chromosomal breakage points could be determined more precisely than by microsatellite analysis. Our results were compared with both the gold standard, microsatellite analysis and SNPtrio, another program available for UPD detection. UPDtool is platform independent, light weight and flexible. Because of its simple input format, UPDtool may also be used with other high-throughput technologies (e.g., next-generation sequencing).
AVAILABILITY AND IMPLEMENTATION: UPDtool executables, documentation and examples can be downloaded from http://www.uni-tuebingen.de/uni/thk/de/f-genomik-software.html.

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Year:  2013        PMID: 23589652     DOI: 10.1093/bioinformatics/btt174

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


  12 in total

1.  Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism.

Authors:  Joanna Yuet-Ling Tung; Sophie Hon Yu Lai; Sandy Leung Kuen Au; Kit San Yeung; Anita Sik Yau Kan; Florence Loong; Diva D DeLeón; Jennifer M Kalish; Arupa Ganguly; Brian Hon Yin Chung; Kelvin Yuen Kwong Chan
Journal:  Int J Pediatr Endocrinol       Date:  2020-07-10

2.  Genome-wide UPD screening in patients with intellectual disability.

Authors:  Christopher Schroeder; Arif Bülent Ekici; Ute Moog; Ute Grasshoff; Ulrike Mau-Holzmann; Marc Sturm; Vanessa Vosseler; Sven Poths; Gudrun Rappold; Angelika Riess; Olaf Riess; Andreas Dufke; Michael Bonin
Journal:  Eur J Hum Genet       Date:  2014-05-07       Impact factor: 4.246

3.  Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing.

Authors:  Thomas Eggermann; Ann-Kathrin Heilsberg; Susanne Bens; Reiner Siebert; Jasmin Beygo; Karin Buiting; Matthias Begemann; Lukas Soellner
Journal:  J Mol Med (Berl)       Date:  2014-07       Impact factor: 4.599

4.  Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analyses.

Authors:  Florian Erger; Karin Burau; Michael Elsässer; Katharina Zimmermann; Ute Moog; Christian Netzer
Journal:  Eur J Hum Genet       Date:  2018-06-11       Impact factor: 4.246

5.  Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array.

Authors:  Mayuko Tamura; Tsuyoshi Isojima; Minae Kawashima; Hideki Yoshida; Keiko Yamamoto; Taichi Kitaoka; Noriyuki Namba; Akira Oka; Keiichi Ozono; Katsushi Tokunaga; Sachiko Kitanaka
Journal:  PLoS One       Date:  2015-07-08       Impact factor: 3.240

6.  A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders.

Authors:  Daniel A King; Tomas W Fitzgerald; Ray Miller; Natalie Canham; Jill Clayton-Smith; Diana Johnson; Sahar Mansour; Fiona Stewart; Pradeep Vasudevan; Matthew E Hurles
Journal:  Genome Res       Date:  2013-12-19       Impact factor: 9.043

7.  Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction.

Authors:  Sandra Chantot-Bastaraud; Svea Stratmann; Frédéric Brioude; Matthias Begemann; Miriam Elbracht; Luitgard Graul-Neumann; Madeleine Harbison; Irène Netchine; Thomas Eggermann
Journal:  Mol Cytogenet       Date:  2017-07-25       Impact factor: 2.009

8.  Mendelian Inconsistent Signatures from 1314 Ancestrally Diverse Family Trios Distinguish Biological Variation from Sequencing Error.

Authors:  Prachi Kothiyal; Wendy S W Wong; Dale L Bodian; John E Niederhuber
Journal:  J Comput Biol       Date:  2019-04-03       Impact factor: 1.479

9.  Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families.

Authors:  Anne S Soehn; Tim W Rattay; Stefanie Beck-Wödl; Karin Schäferhoff; David Monk; Marion Döbler-Neumann; Konstanze Hörtnagel; Agatha Schlüter; Montserrat Ruiz; Aurora Pujol; Stephan Züchner; Olaf Riess; Rebecca Schüle; Peter Bauer; Ludger Schöls
Journal:  Neurology       Date:  2016-06-17       Impact factor: 9.910

10.  Application of chromosomal microarray to investigate genetic causes of isolated fetal growth restriction.

Authors:  Gang An; Yuan Lin; Liang Pu Xu; Hai Long Huang; Si Ping Liu; Yan Hong Yu; Fang Yang
Journal:  Mol Cytogenet       Date:  2018-06-04       Impact factor: 2.009

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