Cost effective assay choice for rare disease study designs

被引:2
作者
Campbell, Desmond D. [1 ,2 ]
Porsch, Robert M. [1 ]
Cherny, Stacey S. [1 ,2 ,4 ]
Capra, Valeria [5 ]
Merello, Elisa [5 ]
De Marco, Patrizia [5 ]
Sham, Pak C. [1 ,2 ]
Garcia-Barcelo, Maria-Merce [3 ]
机构
[1] Univ Hong Kong, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Ctr Genom Sci, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Hong Kong, Hong Kong, Peoples R China
[5] Ist Giannina Gaslini, I-16148 Genoa, Italy
关键词
WES; WGS; High-throughput assay; Rare disease; Study design; MUTATIONS; ASSOCIATION; VARIANTS;
D O I
10.1186/s13023-015-0226-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
High throughput assays tend to be expensive per subject. Often studies are limited not so much by the number of subjects available as by assay costs, making assay choice a critical issue. We have developed a framework for assay choice that maximises the number of true disease causing mechanisms 'seen', given limited resources. Although straightforward, some of the ramifications of our methodology run counter to received wisdom on study design. We illustrate our methodology with examples, and have built a website allowing calculation of quantities of interest to those designing rare disease studies.
引用
收藏
页数:8
相关论文
共 28 条
  • [1] [Anonymous], HUM GENET EMBRYOL
  • [2] [Anonymous], RARE DIS STUDY CALCU
  • [3] [Anonymous], GENOME RES
  • [4] [Anonymous], CAUSES M J EPIDEMIOL
  • [5] NEUROCRISTOPATHIES - UNIFYING CONCEPT OF DISEASE ARISING IN NEURAL CREST MALDEVELOPMENT
    BOLANDE, RP
    [J]. HUMAN PATHOLOGY, 1974, 5 (04) : 409 - 429
  • [6] Rare-disease genetics in the era of next-generation sequencing: discovery to translation
    Boycott, Kym M.
    Vanstone, Megan R.
    Bulman, Dennis E.
    MacKenzie, Alex E.
    [J]. NATURE REVIEWS GENETICS, 2013, 14 (10) : 681 - 691
  • [7] Estimating the human mutation rate using autozygosity in a founder population
    Campbell, Catarina D.
    Chong, Jessica X.
    Malig, Maika
    Ko, Arthur
    Dumont, Beth L.
    Han, Lide
    Vives, Laura
    O'Roak, Brian J.
    Sudmant, Peter H.
    Shendure, Jay
    Abney, Mark
    Ober, Carole
    Eichler, Evan E.
    [J]. NATURE GENETICS, 2012, 44 (11) : 1277 - 1281
  • [8] Large Numbers of Genetic Variants Considered to be Pathogenic are Common in Asymptomatic Individuals
    Cassa, Christopher A.
    Tong, Mark Y.
    Jordan, Daniel M.
    [J]. HUMAN MUTATION, 2013, 34 (09) : 1216 - 1220
  • [9] Origins and functional impact of copy number variation in the human genome
    Conrad, Donald F.
    Pinto, Dalila
    Redon, Richard
    Feuk, Lars
    Gokcumen, Omer
    Zhang, Yujun
    Aerts, Jan
    Andrews, T. Daniel
    Barnes, Chris
    Campbell, Peter
    Fitzgerald, Tomas
    Hu, Min
    Ihm, Chun Hwa
    Kristiansson, Kati
    MacArthur, Daniel G.
    MacDonald, Jeffrey R.
    Onyiah, Ifejinelo
    Pang, Andy Wing Chun
    Robson, Sam
    Stirrups, Kathy
    Valsesia, Armand
    Walter, Klaudia
    Wei, John
    Tyler-Smith, Chris
    Carter, Nigel P.
    Lee, Charles
    Scherer, Stephen W.
    Hurles, Matthew E.
    [J]. NATURE, 2010, 464 (7289) : 704 - 712
  • [10] Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
    de Ligt, Joep
    Willemsen, Marjolein H.
    van Bon, Bregje W. M.
    Kleefstra, Tjitske
    Yntema, Helger G.
    Kroes, Thessa
    Vulto-van Silfhout, Anneke T.
    Koolen, David A.
    de Vries, Petra
    Gilissen, Christian
    del Rosario, Marisol
    Hoischen, Alexander
    Scheffer, Hans
    de Vries, Bert B. A.
    Brunner, Han G.
    Veltman, Joris A.
    Vissers, Lisenka E. L. M.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (20) : 1921 - 1929