Evaluating the harmonisation potential of diverse cohort datasets.
Evaluating the harmonisation potential of diverse cohort datasets.
复制标题
DOI:
10.1007/s10654-023-00997-3
复制
发表时间:
2023-06
影响因子:
13.6
通讯作者:
Gallacher, John
中科院分区:
文献类型:
--
作者:
Bauermeister, Sarah;Phatak, Mukta;Sparks, Kelly;Sargent, Lana;Griswold, Michael;McHugh, Caitlin;Nalls, Mike;Young, Simon;Bauermeister, Joshua;Elliott, Paul;Steptoe, Andrew;Porteous, David;Dufouil, Carole;Gallacher, John
Data discovery, the ability to find datasets relevant to an analysis, increases scientific opportunity, improves rigour and accelerates activity. Rapid growth in the depth, breadth, quantity and availability of data provides unprecedented opportunities and challenges for data discovery. A potential tool for increasing the efficiency of data discovery, particularly across multiple datasets is data harmonisation.A set of 124 variables, identified as being of broad interest to neurodegeneration, were harmonised using the C-Surv data model. Harmonisation strategies used were simple calibration, algorithmic transformation and standardisation to the Z-distribution. Widely used data conventions, optimised for inclusiveness rather than aetiological precision, were used as harmonisation rules. The harmonisation scheme was applied to data from four diverse population cohorts.Of the 120 variables that were found in the datasets, correspondence between the harmonised data schema and cohort-specific data models was complete or close for 111 (93%). For the remainder, harmonisation was possible with a marginal a loss of granularity.Although harmonisation is not an exact science, sufficient comparability across datasets was achieved to enable data discovery with relatively little loss of informativeness. This provides a basis for further work extending harmonisation to a larger variable list, applying the harmonisation to further datasets, and incentivising the development of data discovery tools. The online version contains supplementary material available at 10.1007/s10654-023-00997-3.
登录
查看更多内容
DOI:
10.1186/s13195-017-0288-0
发表时间:
2017-08-29
期刊:
Alzheimer's research & therapy
影响因子:
--
作者:
Dufouil C;Dubois B;Vellas B;Pasquier F;Blanc F;Hugon J;Hanon O;Dartigues JF;Harston S;Gabelle A;Ceccaldi M;Beauchet O;Krolak-Salmon P;David R;Rouaud O;Godefroy O;Belin C;Rouch I;Auguste N;Wallon D;Benetos A;Pariente J;Paccalin M;Moreaud O;Hommet C;Sellal F;Boutoleau-Bretonniére C;Jalenques I;Gentric A;Vandel P;Azouani C;Fillon L;Fischer C;Savarieau H;Operto G;Bertin H;Chupin M;Bouteloup V;Habert MO;Mangin JF;Chêne G;MEMENTO cohort Study Group
通讯作者:
MEMENTO cohort Study Group
影响因子:
7.7
作者:
Steptoe, Andrew;Breeze, Elizabeth;Nazroo, James
通讯作者:
Nazroo, James
影响因子:
7.7
作者:
Smith, Blair H.;Campbell, Archie;Morris, Andrew D.
通讯作者:
Morris, Andrew D.
影响因子:
13.6
作者:
Pinot de Moira A;Haakma S;Strandberg-Larsen K;van Enckevort E;Kooijman M;Cadman T;Cardol M;Corpeleijn E;Crozier S;Duijts L;Elhakeem A;Eriksson JG;Felix JF;Fernández-Barrés S;Foong RE;Forhan A;Grote V;Guerlich K;Heude B;Huang RC;Järvelin MR;Jørgensen AC;Mikkola TM;Nader JLT;Pedersen M;Popovic M;Rautio N;Richiardi L;Ronkainen J;Roumeliotaki T;Salika T;Sebert S;Vinther JL;Voerman E;Vrijheid M;Wright J;Yang TC;Zariouh F;Charles MA;Inskip H;Jaddoe VWV;Swertz MA;Nybo Andersen AM;LifeCycle Project Group
通讯作者:
LifeCycle Project Group
影响因子:
7.7
作者:
O'Connor, Meredith;Moreno-Betancur, Margarita;Goldfeld, Sharon;Wake, Melissa;Patton, George;Dwyer, Terence;Tang, Mimi L. K.;Saffery, Richard;Craig, Jeffrey M.;Loke, Jane;Burgner, David;Olsson, Craig A.;Investigators, LifeCourse Cohort
通讯作者:
Investigators, LifeCourse Cohort