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Nanopore targeted sequencing of the CFTR gene in Moroccan patients with suspected cystic fibrosis

This dataset contains fastq files sequencing with Oxford Nanopore (MK1C)

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DUO:0000012
version: 2021-02-23

research specific restrictions

This data use modifier indicates that use is limited to studies of a certain research type.

DUO:0000016
version: 2021-02-23

genetic studies only

This data use modifier indicates that use is limited to genetic studies only (i.e., studies that include genotype research alone or both genotype and phenotype research, but not phenotype research exclusively)

DUO:0000018
version: 2021-02-23

not for profit, non commercial use only

This data use modifier indicates that use of the data is limited to not-for-profit organizations and not-for-profit use, non-commercial use.

DUO:0000042
version: 2021-02-23

general research use

This data use permission indicates that use is allowed for general research use for any research purpose.

DUO:0000043
version: 2021-02-23

clinical care use

This data use modifier indicates that use is allowed for clinical use and care.

LRS_CFTR gene sequencing_Moroccan cohort

Access to the human genetic data generated from the CFTR gene sequencing study of Moroccan cystic fibrosis patients at the University of Bern is restricted to protect participant confidentiality and comply with ethical and legal regulations. These data are considered sensitive because they may contain potentially identifiable genetic information. Access will be granted only to qualified researchers for legitimate scientific purposes, following review and approval by the Data Access Committee (DAC). Approved researchers must submit a Data Access Agreement outlining the intended use of the data and must agree not to attempt reidentification of participants, not to share the data with third parties, and to maintain it securely in accordance with institutional and legal requirements. All data use must comply with participant consent, ethical approvals, and applicable data protection legislation. For any inquiries or data access requests, please contact: nada.elmakhzen@unibe.ch

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS50000001423 Resequencing

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Quality Report
Located in
EGAF50000500106 fastq.gz 578.3 MB
EGAF50000500107 fastq.gz 761.5 MB
EGAF50000500108 fastq.gz 597.9 MB
EGAF50000500109 fastq.gz 606.7 MB
EGAF50000500110 fastq.gz 154.1 MB
EGAF50000500111 fastq.gz 146.7 MB
EGAF50000500112 fastq.gz 550.1 MB
EGAF50000500113 fastq.gz 146.3 MB
EGAF50000500114 fastq.gz 524.3 MB
9 Files (4.1 GB)