Proposal summaries

These are research proposals that have been approved by the ALSPAC exec. The titles include a B number which identifies the proposal and the date on which the proposals received ALSPAC exec approval.

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B2545 - Reaction time variability as a risk marker

B number: 
B2545
Principal applicant name: 
Richard J. Linscott | Department of Psychology, University of Otago (New Zealand)
Co-applicants: 
Mr Simon Wallace, Ms Michela Verwey, Ms Alannah Corson Keogh, Assoc. Prof. Martin Sellbom
Title of project: 
Reaction time variability as a risk marker
Proposal summary: 

Intra-individual variability (IIV), a measure of transient within-person fluctuations in behavioural performance, is thought to reflect the stability of cognitive processing. Increased IIV is commonly observed in persons diagnosed with schizophrenia. However, the clinical significance of increased IIV is unclear for several reasons. IIV is associated with ADHD and general cognitive impairment; IIV typically changes through the life-span, and characteristically exhibits a decrease from early childhood through to adolescence. The objective of this project is to assess the relationship between IIV and psychotic experiences in children and adolescents, and the extent to which these associations are independent of developmental stage, cognitive impairments, and other potential confounders.

Date proposal received: 
Monday, 28 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Mental health - Psychology, Psychiatry, Cognition, Cognitive impairment, Mental health, Statistical methods, Cognition - cognitive function, Psychology - personality, Psychosis.

B2546 - Assortative mating in the UK population

B number: 
B2546
Principal applicant name: 
David Hugh-Jones | University of East Anglia (UK)
Co-applicants: 
Dr Beate St Pourcain
Title of project: 
Assortative mating in the UK population
Proposal summary: 

Inequality is transmitted across generations, with the children of rich parents doing better than those from poorer households. But why is this? One factor that can exacerbate it is the level of sorting in society. If wealthy and educated people form households with other wealthy, educated people, they can transmit a double dose of advantage to their children. Some of this advantage could even be genetic - for example, height is influenced by genes, and tall people do well in the labour market.

We'll look at how people "assort" with others, including whether people are genetically similar to their partners. This will help us understand how inequality works in the UK - and how the process may change over time, as marriage and labour market institutions alter.

Date proposal received: 
Thursday, 24 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Social Science, GWAS, Statistical methods, See Domingue et al. (2014) for techniques to estimate GAM.

B2538 - Air Pollution Risk and Genetic Liability for Autism and ADHD

B number: 
B2538
Principal applicant name: 
Amy Kalkbrenner | University of Wisconsin-Milwaukee (USA)
Co-applicants: 
Evie Stergiakouli, Christine Ladd-Acosta
Title of project: 
Air Pollution Risk and Genetic Liability for Autism and ADHD
Proposal summary: 

We will investigate whether exposure to air pollution from traffic during pregnancy or early childhood, leads to increased risk or severity of developmental disorders such as autism or attention deficits. We will additionally evaluate whether certain individuals are more at risk or are protected from these impacts due to their genetic make-up.

Date proposal received: 
Tuesday, 22 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Epidemiology, Developmental disorders - autism, Attention deficits, Statistical methods, Environment - enviromental exposure, pollution, Autism Air pollution ADHD Gene-environment interaction

B2540 - Dopamine related polymorphisms in healthy memory and dementia

B number: 
B2540
Principal applicant name: 
John Grogan | University of Bristol (Bristol)
Co-applicants: 
Dr Tom Gaunt
Title of project: 
Dopamine related polymorphisms in healthy memory and dementia
Proposal summary: 

Dopamine is a chemical in the brain involved in reward, pleasure, addiction, and memory. Recent evidence has linked it to memory performance, and even affecting memory decline in dementia patients. We will look to see if genetic differences that affect dopamine activity affect memory performance over time (i.e. does having higher levels of dopamine slow memory decline over age) and dementia progression.

Date proposal received: 
Monday, 21 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Epidemiology, Computer simulations/modelling/algorithms, Statistical methods, Linear regressions will be used to determine association between outcomes and exposures, adjusting for "confounders" where appropriate., Ageing, Cognition - cognitive function, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc., Neurology

B2539 - A genetic underpinning of Optimism - 02/10/2015

B number: 
B2539
Principal applicant name: 
Robyn Wootton | Integrative Epidemiology Unit, University of Bristol (United Kingdom)
Co-applicants: 
Ms Robyn Wootton
Title of project: 
A genetic underpinning of Optimism
Proposal summary: 

Optimism is a complex behavioural trait estimated to be around 40% heritable. This is supposed to be the result of many genes of small effects, as well as complex environmental interactions. This study uses the method of genome-wide association studies (GWAS) to search for single nucleotide polymorphisms (SNPs - specific common variation found in DNA) which relates to levels of optimism and hopefulness. A GWAS of optimism in a sample of twins (TEDS) found two genetic markers known as single nucleotide polymorphisms (SNPS) to be associated.

The next stage of this research is to see if these significant SNPs are replicable in the ALSPAC sample. The overall aim of the research is to be able to better understand what characterises positive psychological aspects of wellbeing and use this information to better inform wellbeing interventions.

Date proposal received: 
Friday, 18 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Genetics

B2541 - Social Origins Cognitive Ability and Educational Attainment A Birth Cohort and Life-Course Perspective

B number: 
B2541
Principal applicant name: 
Mollie Bourne | Department of Social Policy and Intervention, University of Oxford
Co-applicants: 
Dr Erzsebet Bukodi, Dr John Goldthorpe, Bastian Betthaeuser
Title of project: 
Social Origins, Cognitive Ability and Educational Attainment: A Birth Cohort and Life-Course Perspective
Proposal summary: 

If one takes children who at an early age had similar scores on tests of their cognitive ability, one still finds significant differences in their later life educational attainment. How far are these differences related to their social origins? This is the overarching research question that we address – in more detail than in previous work and with reference to the twenty-first as well as to the twentieth century. To do so, we will use data relating to cohorts of children born in 1946, 1958, 1970 and the early 1990s. These data contain detailed information on the results of individuals’ performance on tests of cognitive ability at around age 10, on their parents’ social class, status and education – i.e. on their families’ economic, socio-cultural and specifically educational resources – and also on their own educational careers through into adult life and on the qualifications, academic and vocational, that they have obtained. On this basis, we will be able to give an answer to the question posed above: that is, by comparing, for each cohort, the subsequent educational attainment of children who at around age 10 were of similar ability and by ascertaining how far differences in their attainment are associated with their social origins. This question is of major academic interest in the field of social mobility. But it is also highly relevant to a range of current policy issues relating to the most effective means of offsetting the effects of disadvantaged social origins on individuals’ educational and subsequent socioeconomic attainment.

Date proposal received: 
Wednesday, 16 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Social Science

B2507 - Replication of interaction between dietary fish intake and genetic variants for gestational weight gain - 02/10/2015

B number: 
B2507
Principal applicant name: 
Lavinia Paternoster | MRC IEU, SSCM, University of Bristol (United Kingdom)
Co-applicants: 
Charles Laurin, Lars Henrik Ängquist
Title of project: 
Replication of interaction between dietary fish intake and genetic variants for gestational weight gain
Proposal summary: 

A study in the Danish National Birth Cohort (DNBC) has identified an interaction between the PPARG Pro12Ala variant and dietary fish intake in association with gestational weight gain. We aim to replicate this association in ALSPAC.

Date proposal received: 
Wednesday, 9 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Genetics, Pregnancy - e.g. reproductive health, postnatal depression, birth outcomes, etc., Statistical methods, Birth outcomes, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc., Nutrition - breast feeding, diet

B2542 - Does atopic disease impact later educational and occupational attainment

B number: 
B2542
Principal applicant name: 
Sinead Langan | London School of Hygiene and Tropical Medicine (United Kingdom)
Co-applicants: 
Liam Smeeth , Katrine Abuabara, Martin McKee
Title of project: 
Does atopic disease impact later educational and occupational attainment?
Proposal summary: 

The burden of atopic diseases is quickly rising.[1] The focus in most published research is on medical outcomes, rather than a holistic approach, focusing on the wider impact of atopy on social outcomes.

Data are conflicting regarding atopic diseases and educational attainment. No study has assessed the effect of the three major atopic diseases simultaneously. Although these diseases frequently co-occur, understanding the most predictive phenotypes is important to tailoring interventions. Previous studies have demonstrated that children with rhinitis were 40% more likely to drop a grade between winter and final GCSE examinations, and 70% more likely to drop a grade if they were taking sedating antihistamines during examinations.[3] There are no studies of the effect of childhood eczema on educational attainment. There are contrasting study findings in asthma, with some studies of asthma reporting no effect, adverse effects, and some describing a benefit in terms of exam results. A recent study reported that social adversity and ethnicity was associated with poor exam performance, while asthma was associated with 1.1% increase in exam scores.[4]
Multiple factors may lead to worsened educational attainment. These include absenteeism from school due to ill health. Atopic diseases can also lead to “presenteeism” and poor concentration at school. Depression and anxiety, sleeplessness and ADHD have been associated with eczema and may lead to impaired educational attainment. Medication use including antihistamines and oral corticosteroid use could impact educational outcomes and thus hinder later occupational attainment.

Existing birth cohort data have the potential to answer many critical questions in relation to educational and occupational attainment. We will utilize ALSPAC data to test the hypothesis that atopic diseases are associated with worse education and occupational attainment.

Date proposal received: 
Monday, 7 September, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Epidemiology

B2519 - Prevalence of Chlamydia in young adulthood

B number: 
B2519
Principal applicant name: 
John Macleod | ALSPAC (United Kingdom)
Co-applicants: 
Title of project: 
Prevalence of Chlamydia in young adulthood
Proposal summary: 

Chlamydia is a common Sexually Transmitted Infection (STI) that often has no symptoms so is not recognised and treated. Untreated Chlamydia can have serious reproductive health consequences in women and because of this we have a National Chlamydia Screening Programme. There are still many unanswered questions about risk factors for Chlamydia, influences on participation in screening and long term health effects of infection. Participants in the ALSPAC TF4 clinic were offered Chlamydia testing within the National Screening Programme. This found that infection was less common than in previous surveys but that infection was much more common in people experiencing social disadvantage. We want to study whether this is still true at age 24 and also lay the groundwork for later studies looking at long term effects of Chlamydia. We also want to add information from Chlamydia tests in the Age 24 clinic to other information we have on infection over the lifetime from previous tests, questionnaires and blood tests to build a full picture of lifetime infection with Chlamydia and the effects of this on health.

Date proposal received: 
Monday, 24 August, 2015
Date proposal approved: 
Friday, 2 October, 2015
Keywords: 
Epidemiology, Sexually transmitted diseases, chlamydia, gonorrhoea, Statistical methods, Nucleic Acid Amplification Testing, Biological samples -e.g. blood, cell lines, saliva, etc., Chlamydia, sexual health

B2520 - Psychological adjustment to chronic illness in youth A longitudinal exploration of emerging mental health issues

B number: 
B2520
Principal applicant name: 
Ann Marie Brady | Queen Mary University of London (United Kingdom)
Co-applicants: 
Dr. Jessica Deighton, Miss Ann Marie Brady
Title of project: 
Psychological adjustment to chronic illness in youth: A longitudinal exploration of emerging mental health issues
Proposal summary: 

The World Health Organisation has defined the current era as one of epidemiological transition, where chronic medical issues are overtaking acute and even infectious disease as one of the most significant challenges facing health care providers internationally. Healthcare providers are struggling to provide the necessary medical resources needed to treat the growing population of people living with long-term health issues over a prolonged period of time – for example, in 2012, the Department of Health estimated that 70% of the annual healthcare in England spend could be attributed to those living with long-term conditions, and estimated that this figure would only rise in the coming decades. Highly implicit in these costs are the mental health issues which are disproportionately prevalent among this population. Co-morbid mental illness in the context of chronic physical illness has been established to lead to poorer physical health outcomes, decreased quality of life and increased healthcare expenditure. Therefore, interventions to reduce the burden of chronic illness in recent years have become increasingly focused on improving the well-being of people living with long-term medical issues.

Children and adolescents have been noticeably absent in the larger discourse on chronic illness and its related consequences. However, such an exclusion is severely curtailing our understanding of the course of chronic illness, especially when it comes to understanding the development of mental health issues among this population. In the general population, epidemiologists have been unable to establish whether it is chronic illness that causes the individual to become mentally distressed, or whether it is mental health issues, although they may not be diagnosed, that give rise to a number of behaviours which puts the individual at an increased risk for developing chronic illness. However, lifestyle factors cannot modify the development of chronic health conditions in younger populations, meaning that a disproportionate occurrence of mental health conditions would indicate some factor, specifically relating to living with chronic illness, that mediates the occurrence of mental health issues in this age group. Therefore, a specific focus on younger age groups could provide unique insight into critical factors mediating the relationship between chronic illness and mental health, in order to guide the provision of effective interventions both to this age group, and people living with long-term illness more generally. However, there are such significant limitations to the quality of the existing research focusing on mental health issues in chronically ill youths, that it cannot even be established that a disproportionate level of mental health issues truly exists among this population. This research project aims to address the limitations in previous research, in order to more thoroughly investigate the relationship between living with a chronic illness in childhood and adolescence and consequent psychological adjustment.

Date proposal received: 
Wednesday, 29 July, 2015
Date proposal approved: 
Wednesday, 30 September, 2015
Keywords: 
Epidemiology, Behaviour - e.g. antisocial behaviour, risk behaviour, etc., Bone disorders - arthritis, osteoporosis, Diabetes, Gastrointestinal, Mental health, Obesity, Pain, Respiratory - asthma, Statistical methods, Childhood - childcare, childhood adversity, Development, Psychology - personality, Physical - activity, fitness, function, Chronic Illness; Chronic Disease; Chronic Medical Issues

B2532 - Abnormal metabolic measures in adolescents with pyschotic experiences - 24/09/2015

B number: 
B2532
Principal applicant name: 
Nomi Werbeloff (UCL, Division of Psychiatry, UK)
Co-applicants: 
David Osborn (UCL, Division of Psychiatry, UK), Joseph F Hayes (UCL, Division of Psychiatry, UK)
Title of project: 
Abnormal metabolic measures in adolescents with pyschotic experiences
Proposal summary: 

To examine whether people with psychotic experiences at age 18 are more likely to have abnormal metabolic measures in the period preceding the onset of such symptoms, and at what time point are these abnormalities evident. If there will be evidence of an association between metabolic disorders and psychotic experiences, we will then examine whether this association is specific to psychotic experiences or occurs across a range of psychiatric disorders.

Date proposal received: 
Friday, 11 September, 2015
Date proposal approved: 
Thursday, 24 September, 2015
Keywords: 
Metabolomics, Psychology
Primary keyword: 

2527 - The Cultural Transmission of BMI

B number: 
2527
Principal applicant name: 
Stacey Cherny | University of Hong Kong (Hong Kong)
Co-applicants: 
Prof. Pak Chung Sham
Title of project: 
The Cultural Transmission of BMI
Proposal summary: 

The body mass index (BMI) has long been used in population studies in order to quantify obesity
and is known to predict cardiovascular events. Especially in childhood BMI the influence of family environment has attracted considerable interest. Thus previous research has shown that maternal BMI is an excellent predictor for the BMI of the offspring. However, it is unclear to what extent maternal genetic factors contribute to the offspring’s BMI beyond genetic transmission. This effect is also called cultural transmission (CT) and can be defined as the transmission of environmental factors from the parent to the offspring generation. CT can be divided into two components. Environmental influence caused by parental genetic factors
and components transmitted exclusively via the environment. Thus the aim of this proposal is to
partition CT into genetic and environmental aspects to further elucidate the maternal influence
on BMI.

Date proposal received: 
Friday, 4 September, 2015
Date proposal approved: 
Thursday, 24 September, 2015
Keywords: 
Statistics/methodology, Obesity, Epigenetics, GWAS, Statistical methods, BMI, Environment - enviromental exposure, pollution, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc., Statistical methods

B2526 - Vitamin D status and adiposity in school-age children - 24/09/2015

B number: 
B2526
Principal applicant name: 
Rebecca Richmond | MRC Integrative Epidemiology Unit, University of Bristol (UK)
Co-applicants: 
Trudy Voortman, Miss Rebecca Richmond
Title of project: 
Vitamin D status and adiposity in school-age children
Proposal summary: 

Vitamin D deficiency has been associated with adiposity in adults and adolescents. However, there is limited information about this association in young children and the direction of causality.

Date proposal received: 
Thursday, 3 September, 2015
Date proposal approved: 
Thursday, 24 September, 2015
Keywords: 
Epidemiology

B2522 - Generation of summary linkage disequilibrium statistics for gene set enrichment analysis using the ALSPAC genotype data - 24/09/2015

B number: 
B2522
Principal applicant name: 
Beate St Pourcain | MRCIEU, MPI for Psycholinguistics
Co-applicants: 
Johannes Waage, Simon Fisher
Title of project: 
Generation of summary linkage disequilibrium statistics for gene set enrichment analysis using the ALSPAC genotype data
Proposal summary: 

This project extends research collaborations with COPSAC within the UK10K project. The project will generate a summary of genetic relationships between genetic variants, which will help to improve the power of gene-set enrichment analyses. The summary of genetic relationships will be available to ALSPAC users and shared with COPSAC.

Date proposal received: 
Tuesday, 1 September, 2015
Date proposal approved: 
Thursday, 24 September, 2015
Keywords: 
Genetics, Statistical methods, Gene set enrichment analysis

B2536 - Genetic risk factors for childhood dental caries - 18/09/2015

B number: 
B2536
Principal applicant name: 
Simon Haworth | MRC IEU, Bristol (Bristol)
Co-applicants: 
Mr Simon Haworth
Title of project: 
Genetic risk factors for childhood dental caries
Proposal summary: 

Dental caries (decay) is a common disease in children. The consequences of dental caries include pain and infection and this has a major impact on children and their families. In severe cases children may require a general anaesthetic for removal of decayed teeth. Dental caries runs in families and about 50% of the risk of caries is due to genetic factors. Despite this, the individual genetic factors responsible are not well understood, probably because previous studies have been too small to find individual genetic factors. We have been asked to contribute data from ALSPAC to a new analysis, which will have a larger overall study size than previous analyses, and a greater chance of finding new genetic factors.

Date proposal received: 
Wednesday, 16 September, 2015
Date proposal approved: 
Friday, 18 September, 2015
Keywords: 
Epidemiology, Dental caries, GWAS, Childhood - childcare, childhood adversity, Dental, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc.

B2535 - Lifecourse epidemiological investigations of Eyes and Vision CLOSER workpackage 4

B number: 
B2535
Principal applicant name: 
Jugnoo S Rahi | UCL Institute of Child Health (UK)
Co-applicants: 
Phillippa Cumberland, Antonietta Chianca, Cathy Williams, Prof Jez Guggenheim
Title of project: 
Lifecourse epidemiological investigations of Eyes and Vision (CLOSER workpackage 4)
Proposal summary: 

Refractive error (e.g. myopia) is an important public health concern worldwide, as the most common cause of impaired vision. There is increasing interest in the affect of social position on visual health, considering the whole range of severity including those with mild impairment. ALSPAC is included in our programme of work within CLOSER (Cohort & Longitudinal Studies Enhancement Resource) which is investigating visual function and refractive error, making comparisons both within and across UK-based cohort and longitudinal studies. We will apply life course epidemiological approaches to investigate biological, environmental and lifestyle factors influencing the development of refractive error and the biological and social factors that influence visual health. We will also investigate the health and social outcomes associated with impaired visual health and with refractive error. Using several studies, which started recruitment at different times, we will assess any changes over time in both risk factors and outcomes which may help to identify modifiable risk factors.

Date proposal received: 
Tuesday, 15 September, 2015
Date proposal approved: 
Friday, 18 September, 2015
Keywords: 
Ophthalmology, Refractive error, specifically myopia, and visual impairment, Statistical methods, Life course epidemiology, Statistical methods, Vision, visual acuity, refractive error, self-report

B2530 - statistical method development and application for genetic fine mapping using meta-analysis summary statistics - 18/09/2015

B number: 
B2530
Principal applicant name: 
Jie Zheng | MRC IEU (UK)
Co-applicants: 
Dr. Tom Gaunt, Dr. Santiago Rodriguez , Prof Dave Evans
Title of project: 
statistical method development and application for genetic fine mapping using meta-analysis summary statistics
Proposal summary: 

This project is aiming to develop a genetic fine mapping tool (HAPRAP) using meta-analysis summary statistics only. The method can be used as a model selection approach for 2 sample MR.
We are also aiming to apply HAPRAP to all public available GWAS meta-analysis summary statistics.

Date proposal received: 
Thursday, 10 September, 2015
Date proposal approved: 
Friday, 18 September, 2015
Keywords: 
Genetics, GWAS, Statistical methods, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc., Statistical methods

B2528 - The impact of cycle proficiency training on cycle-related behaviours and accidents in adolescence - 18/09/2015

B number: 
B2528
Principal applicant name: 
Alison Teyhan | University of Bristol (United Kingdom)
Co-applicants: 
John Macleod, Rosie Cornish, Andy Boyd
Title of project: 
The impact of cycle proficiency training on cycle-related behaviours and accidents in adolescence
Proposal summary: 

Education is one strategy to reduce cycle-related accidents, and many countries have training courses for children. In the UK, the National Cycle Proficiency Scheme (NCPS) was first introduced in 1947. A typical course takes place during the final years of primary school and 40% of children participate by their twelfth birthday. Despite the significant resources invested in child cycle training both in the UK and elsewhere, there has been little scientific evaluation of their outcomes.

Date proposal received: 
Tuesday, 8 September, 2015
Date proposal approved: 
Friday, 18 September, 2015
Keywords: 
Epidemiology, Accident prevention; cycle training; cycle behaviours

B2521 - The influence of the onset of puberty on skin pigmentation and sun exposure patterns in pre and post-pubertal children

B number: 
B2521
Principal applicant name: 
Carolina Bonilla | School of Social and Community Medicine (United Kingdom)
Co-applicants: 
Dr. Sarah Lewis
Title of project: 
The influence of the onset of puberty on skin pigmentation and sun exposure patterns in pre and post-pubertal children
Proposal summary: 

Skin pigmentation differs between the sexes. In most populations, women exhibit lighter skin than men, which could be a consequence of requiring greater quantities of vitamin D to support pregnancy and lactation, of having more subcutaneous adipose tissue with less melanogenesis-stimulating androgens than men, and/or of a preference of males for fairer females(1,2). Among pre-pubertal children, however, girls are usually darker than boys, but this appears to reverse at the onset of puberty(1,3). We propose to use genetic variants strongly associated with age at menarche and Tanner stage (a measurement of pubertal development in adolescents)(4,5) to examine the relationship between puberty initiation and pigmentation changes, with particular emphasis on the consequences that these changes bring to sun exposure patterns and vitamin D levels, in ALSPAC children. Additionally, we will assess the role that androgens and estrogens play in eliciting gender pigmentation differences, using a similar framework.

Date proposal received: 
Thursday, 27 August, 2015
Date proposal approved: 
Friday, 11 September, 2015
Keywords: 
Anthropology, skin pigmentation sun exposure, Dermatology, Genetics - e.g. epigenetics, mendelian randomisation, UK10K, sequencing, etc., Hormones - cortisol, IGF, thyroid, Puberty, Sex differences, pigmentation, puberty

B2523 - Using genetic data to re-index ALSPAC and identify new data/samples - 11/09/2015

B number: 
B2523
Principal applicant name: 
Nicholas Timpson | UoB and MRC IEU (Bristol)
Co-applicants: 
Dr George McMahon, Dr Gibran Hemani
Title of project: 
Using genetic data to re-index ALSPAC and identify new data/samples
Proposal summary: 

This project has the simple objective to reassess the current ALSPAC ID system (which summarises individual identification and relatedness through pregnancy identifiers and birth order) using genetic data. Data and sample identification is an ongoing challenge within the ALSPAC study and studies more generally and the availability of genetic data on (in principle) all participants allows for a re-indexing of samples uniquely and relative to each other in terms of relatedness. There is an academic component to this in understanding the level of relatedness (cryptic or otherwise) in this sample and also a practical aim to this in that this will allow (i) the confirmation of existing IDs and (ii) the proper identification of sample relatedness where sample IDs exist, but no information as to the contribution to family status is available. This will be done solely with genetic data and as such will not be subject to administrative error.

Date proposal received: 
Thursday, 27 August, 2015
Date proposal approved: 
Friday, 11 September, 2015
Keywords: 
Genetics

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