Literature DB >> 24746958

Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature.

Zehra Ordulu1, Kristen E Wong2, Benjamin B Currall1, Andrew R Ivanov2, Shahrin Pereira2, Sara Althari3, James F Gusella4, Michael E Talkowski5, Cynthia C Morton6.   

Abstract

With recent rapid advances in genomic technologies, precise delineation of structural chromosome rearrangements at the nucleotide level is becoming increasingly feasible. In this era of "next-generation cytogenetics" (i.e., an integration of traditional cytogenetic techniques and next-generation sequencing), a consensus nomenclature is essential for accurate communication and data sharing. Currently, nomenclature for describing the sequencing data of these aberrations is lacking. Herein, we present a system called Next-Gen Cytogenetic Nomenclature, which is concordant with the International System for Human Cytogenetic Nomenclature (2013). This system starts with the alignment of rearrangement sequences by BLAT or BLAST (alignment tools) and arrives at a concise and detailed description of chromosomal changes. To facilitate usage and implementation of this nomenclature, we are developing a program designated BLA(S)T Output Sequence Tool of Nomenclature (BOSToN), a demonstrative version of which is accessible online. A standardized characterization of structural chromosomal rearrangements is essential both for research analyses and for application in the clinical setting.
Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2014        PMID: 24746958      PMCID: PMC4067557          DOI: 10.1016/j.ajhg.2014.03.020

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  38 in total

1.  BLAT--the BLAST-like alignment tool.

Authors:  W James Kent
Journal:  Genome Res       Date:  2002-04       Impact factor: 9.043

2.  The human genome browser at UCSC.

Authors:  W James Kent; Charles W Sugnet; Terrence S Furey; Krishna M Roskin; Tom H Pringle; Alan M Zahler; David Haussler
Journal:  Genome Res       Date:  2002-06       Impact factor: 9.043

3.  Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.

Authors:  Emma Palmer; Helen Speirs; Peter J Taylor; Glenda Mullan; Gill Turner; Stewart Einfeld; Bruce Tonge; David Mowat
Journal:  Am J Med Genet A       Date:  2013-12-05       Impact factor: 2.802

Review 4.  Next-generation sequencing in the clinic: promises and challenges.

Authors:  Jiekun Xuan; Ying Yu; Tao Qing; Lei Guo; Leming Shi
Journal:  Cancer Lett       Date:  2012-11-19       Impact factor: 8.679

5.  Paris Conference (1971): Standardization in human cytogenetics.

Authors: 
Journal:  Cytogenetics       Date:  1972

6.  Chemical differentiation along metaphase chromosomes.

Authors:  T Caspersson; S Farber; G E Foley; J Kudynowski; E J Modest; E Simonsson; U Wagh; L Zech
Journal:  Exp Cell Res       Date:  1968-01       Impact factor: 3.905

7.  Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis.

Authors:  T Caspersson; M Hultén; J Lindsten; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

8.  An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature.

Authors: 
Journal:  Cytogenet Cell Genet       Date:  1978

9.  Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.

Authors:  Sarah Vergult; Ellen Van Binsbergen; Tom Sante; Silke Nowak; Olivier Vanakker; Kathleen Claes; Bruce Poppe; Nathalie Van der Aa; Markus J van Roosmalen; Karen Duran; Masoumeh Tavakoli-Yaraki; Marielle Swinkels; Marie-José van den Boogaard; Mieke van Haelst; Filip Roelens; Frank Speleman; Edwin Cuppen; Geert Mortier; Wigard P Kloosterman; Björn Menten
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

10.  The Database of Genomic Variants: a curated collection of structural variation in the human genome.

Authors:  Jeffrey R MacDonald; Robert Ziman; Ryan K C Yuen; Lars Feuk; Stephen W Scherer
Journal:  Nucleic Acids Res       Date:  2013-10-29       Impact factor: 16.971

View more
  25 in total

1.  Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.

Authors:  Cinthya J Zepeda-Mendoza; Jonas Ibn-Salem; Tammy Kammin; David J Harris; Debra Rita; Karen W Gripp; Jennifer J MacKenzie; Andrea Gropman; Brett Graham; Ranad Shaheen; Fowzan S Alkuraya; Campbell K Brasington; Edward J Spence; Diane Masser-Frye; Lynne M Bird; Erica Spiegel; Rebecca L Sparkes; Zehra Ordulu; Michael E Talkowski; Miguel A Andrade-Navarro; Peter N Robinson; Cynthia C Morton
Journal:  Am J Hum Genet       Date:  2017-07-20       Impact factor: 11.025

2.  Identification of ROBO1/2 and SCEL as candidate genes in Kallmann syndrome with emerging bioinformatic analysis.

Authors:  Zuobin Zhu; Xiaoxiao Han; Ying Li; Conghui Han; Mengqiong Deng; Yuhao Zhang; Qing Shen; Yijuan Cao; Zhenbei Li; Xitao Wang; Juan Gu; Xiaoyan Liu; Yaru Yang; Qiang Zhang; Fangfang Hu
Journal:  Endocrine       Date:  2019-07-19       Impact factor: 3.633

3.  Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis.

Authors:  Zehra Ordulu; Tammy Kammin; Harrison Brand; Vamsee Pillalamarri; Claire E Redin; Ryan L Collins; Ian Blumenthal; Carrie Hanscom; Shahrin Pereira; India Bradley; Barbara F Crandall; Pamela Gerrol; Mark A Hayden; Naveed Hussain; Bibi Kanengisser-Pines; Sibel Kantarci; Brynn Levy; Michael J Macera; Fabiola Quintero-Rivera; Erica Spiegel; Blair Stevens; Janet E Ulm; Dorothy Warburton; Louise E Wilkins-Haug; Naomi Yachelevich; James F Gusella; Michael E Talkowski; Cynthia C Morton
Journal:  Am J Hum Genet       Date:  2016-10-13       Impact factor: 11.025

4.  Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis†.

Authors:  Kusumika Mukherjee; Kana Ishii; Vamsee Pillalamarri; Tammy Kammin; Joan F Atkin; Scott E Hickey; Qiongchao J Xi; Cinthya J Zepeda; James F Gusella; Michael E Talkowski; Cynthia C Morton; Richard L Maas; Eric C Liao
Journal:  Hum Mol Genet       Date:  2016-01-11       Impact factor: 6.150

5.  Study of structural chromosome abnormalities to increase the understanding of human genetic diversity: a commentary on signature of backward replication slippage at the copy number variation junction.

Authors:  Keiko Wakui
Journal:  J Hum Genet       Date:  2014-10-09       Impact factor: 3.172

6.  Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.

Authors:  M J Macera; A Sobrino; B Levy; V Jobanputra; V Aggarwal; A Mills; C Esteves; C Hanscom; S Pereira; V Pillalamarri; Z Ordulu; C C Morton; M Talkowski; D Warburton
Journal:  Prenat Diagn       Date:  2015-02-04       Impact factor: 3.050

7.  Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin.

Authors:  Cinthya J Zepeda-Mendoza; Alexandra Bardon; Tammy Kammin; David J Harris; Helen Cox; Claire Redin; Zehra Ordulu; Michael E Talkowski; Cynthia C Morton
Journal:  Eur J Hum Genet       Date:  2018-01-10       Impact factor: 4.246

8.  Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation.

Authors:  Daniel Nilsson; Maria Pettersson; Peter Gustavsson; Alisa Förster; Wolfgang Hofmeister; Josephine Wincent; Vasilios Zachariadis; Britt-Marie Anderlid; Ann Nordgren; Outi Mäkitie; Valtteri Wirta; Max Käller; Francesco Vezzi; James R Lupski; Magnus Nordenskjöld; Elisabeth Syk Lundberg; Claudia M B Carvalho; Anna Lindstrand
Journal:  Hum Mutat       Date:  2016-12-05       Impact factor: 4.878

9.  Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome.

Authors:  Ming Lei; Satomi Mitsuhashi; Noriko Miyake; Tohru Ohta; Desheng Liang; Lingqian Wu; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2019-04-15       Impact factor: 3.172

10.  Implication of LRRC4C and DPP6 in neurodevelopmental disorders.

Authors:  Gilles Maussion; Cristiana Cruceanu; Jill A Rosenfeld; Scott C Bell; Fabrice Jollant; Jin Szatkiewicz; Ryan L Collins; Carrie Hanscom; Ilaria Kolobova; Nicolas Menjot de Champfleur; Ian Blumenthal; Colby Chiang; Vanessa Ota; Christina Hultman; Colm O'Dushlaine; Steve McCarroll; Martin Alda; Sebastien Jacquemont; Zehra Ordulu; Christian R Marshall; Melissa T Carter; Lisa G Shaffer; Pamela Sklar; Santhosh Girirajan; Cynthia C Morton; James F Gusella; Gustavo Turecki; Dimitri J Stavropoulos; Patrick F Sullivan; Stephen W Scherer; Michael E Talkowski; Carl Ernst
Journal:  Am J Med Genet A       Date:  2016-10-19       Impact factor: 2.802

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.