Literature DB >> 22228013

The challenges of studying complex and dynamic regions of the human genome.

Edward J Hollox1.   

Abstract

Recent work has emphasised that the human genome is not simple and static, but complex and dynamic. This review focuses on the regions that are particularly hard to dissect and analyse, yet hold clues to how the genome changes during evolution and disease. I begin by summarising recent key advances in the understanding of the variable structure of our genome, and then I discuss a medley of methods that may allow us to analyse this structure in fine detail. In the final part, I describe potential future developments in this field, and make an argument that, just as we routinely genotype single-nucleotide polymorphisms now and will routinely re-sequence genomes in the near future, we should be aiming to physically re-map the individual human genome for each individual we study.

Entities:  

Mesh:

Year:  2012        PMID: 22228013     DOI: 10.1007/978-1-61779-507-7_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

1.  Determination of haplotypes at structurally complex regions using emulsion haplotype fusion PCR.

Authors:  Jess Tyson; John A L Armour
Journal:  BMC Genomics       Date:  2012-12-11       Impact factor: 3.969

2.  Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region.

Authors:  Kiana Mohajeri; Stuart Cantsilieris; John Huddleston; Bradley J Nelson; Bradley P Coe; Catarina D Campbell; Carl Baker; Lana Harshman; Katherine M Munson; Zev N Kronenberg; Milinn Kremitzki; Archana Raja; Claudia Rita Catacchio; Tina A Graves; Richard K Wilson; Mario Ventura; Evan E Eichler
Journal:  Genome Res       Date:  2016-10-07       Impact factor: 9.043

3.  Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs.

Authors:  Bridgett M vonHoldt; Emily Shuldiner; Ilana Janowitz Koch; Rebecca Y Kartzinel; Andrew Hogan; Lauren Brubaker; Shelby Wanser; Daniel Stahler; Clive D L Wynne; Elaine A Ostrander; Janet S Sinsheimer; Monique A R Udell
Journal:  Sci Adv       Date:  2017-07-19       Impact factor: 14.136

4.  Low copy number of the salivary amylase gene predisposes to obesity.

Authors:  Mario Falchi; Julia Sarah El-Sayed Moustafa; Petros Takousis; Francesco Pesce; Amélie Bonnefond; Johanna C Andersson-Assarsson; Peter H Sudmant; Rajkumar Dorajoo; Mashael Nedham Al-Shafai; Leonardo Bottolo; Erdal Ozdemir; Hon-Cheong So; Robert W Davies; Alexandre Patrice; Robert Dent; Massimo Mangino; Pirro G Hysi; Aurélie Dechaume; Marlène Huyvaert; Jane Skinner; Marie Pigeyre; Robert Caiazzo; Violeta Raverdy; Emmanuel Vaillant; Sarah Field; Beverley Balkau; Michel Marre; Sophie Visvikis-Siest; Jacques Weill; Odile Poulain-Godefroy; Peter Jacobson; Lars Sjostrom; Christopher J Hammond; Panos Deloukas; Pak Chung Sham; Ruth McPherson; Jeannette Lee; E Shyong Tai; Robert Sladek; Lena M S Carlsson; Andrew Walley; Evan E Eichler; Francois Pattou; Timothy D Spector; Philippe Froguel
Journal:  Nat Genet       Date:  2014-03-30       Impact factor: 38.330

5.  Understanding the Early Evolutionary Stages of a Tandem Drosophilamelanogaster-Specific Gene Family: A Structural and Functional Population Study.

Authors:  Bryan D Clifton; Jamie Jimenez; Ashlyn Kimura; Zeinab Chahine; Pablo Librado; Alejandro Sánchez-Gracia; Mashya Abbassi; Francisco Carranza; Carolus Chan; Marcella Marchetti; Wanting Zhang; Mijuan Shi; Christine Vu; Shudan Yeh; Laura Fanti; Xiao-Qin Xia; Julio Rozas; José M Ranz
Journal:  Mol Biol Evol       Date:  2020-09-01       Impact factor: 16.240

6.  Systematic transcriptome wide analysis of lncRNA-miRNA interactions.

Authors:  Saakshi Jalali; Deeksha Bhartiya; Mukesh Kumar Lalwani; Sridhar Sivasubbu; Vinod Scaria
Journal:  PLoS One       Date:  2013-02-06       Impact factor: 3.240

7.  Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication.

Authors:  Stuart Cantsilieris; Patrick S Western; Paul N Baird; Stefan J White
Journal:  BMC Genomics       Date:  2014-05-01       Impact factor: 3.969

Review 8.  Genetic Variations in Vesicoureteral Reflux Sequelae.

Authors:  David S Hains; Andrew L Schwaderer
Journal:  Pathogens       Date:  2016-02-02

9.  Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD).

Authors:  Felix Grassmann; Stuart Cantsilieris; Anja-Sabrina Schulz-Kuhnt; Stefan J White; Andrea J Richardson; Alex W Hewitt; Brendan J Vote; Denise Schmied; Robyn H Guymer; Bernhard H F Weber; Paul N Baird
Journal:  J Neuroinflammation       Date:  2016-04-18       Impact factor: 8.322

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.