Study

Multi-omics data of 1000 Inflammatory Bowel Disease patients

Study ID Alternative Stable ID Type
EGAS00001002702 Other

Study Description

Portal available at https://1000ibd.org Inflammatory bowel disease (IBD) is a chronic complex disease of the gastrointestinal (GI) tract. Patients with IBD can experience a wide range of symptoms, but the pathophysiological mechanisms that cause these individual differences in clinical presentation remain largely unknown. In consequence, IBD is currently classified into subtypes using clinical characteristics. If we are to develop a more targeted treatment approach, molecular subtypes of IBD need to be discovered that can be used as new drug targets. To achieve this, we need multiple layers of molecular data are generated from the same IBD patients.We initiated the 1000IBD project to prospectively follow more than 1000 IBD patients from the Northern provinces of the Netherlands. For these patients, we have collected a uniquely large number of phenotypes and generated multi-omics profiles. To date, 1,215 participants have been enrolled in the project and enrolment is on-going, with 609 patients being present in the first data release. Phenotype data collected for these participants ... (Show More)

Study Datasets 5 datasets.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001003935
Sequencing of V4 hypervariable region of 16S gene of microbiota present in feces of IBD patients
315
EGAD00001003936
Sequencing of V4 hypervariable region of 16S gene from microbiota present in intestinal biopsies of IBD patients
107
EGAD00001003991
Complete clinical phenotypic description of all patients; the number listed represents all the samples linked to the 609 patients present in the dataset. Please consult the key file to visualise the sample-patient relationship
1091
EGAD00001004194
Complete Microbiome Metagenomics from feces of 355 IBD patients; The sequencer used was the Illumina HiSeq 2000 with a paired end reads design, reflected in the 2 FastQ format files per sample.
Illumina HiSeq 2000 355
EGAD00010001495
Intensity files for Immunochip genotypes from blood
Illumina Immunochip 314

Who archives the data?

There are no publications available