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Exome Sequencing data from infertility cases.

This dataset includes exome sequencing (ES) from a cohort of patients with infertility. Sequencing was performed on genomic DNA extracted from blood, using Agilent SureSelect XT Low Input exome capture and Illumina NovaSeq 6000 paired-end sequencing and is intended to facilitate research into novel genetic causes of infertility.

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Reproductive failure NGS Data Access Policy (RI-MUHC, Slim Lab)

Access to these controlled human sequencing and phenotype data is restricted to qualified researchers with local REC/IRB approval and an institutional signature on a Data Access Agreement. Permitted uses include research on human reproduction, infertility, gametogenesis, and related biomedical questions. Re-identification is prohibited; data must not be redistributed. Results must be reported in aggregate only; publications must acknowledge the data source.

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
EGAS50000001320 Exome Sequencing

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
EGAF50000451708 fastq.gz 6.3 GB
EGAF50000451709 fastq.gz 6.5 GB
EGAF50000451710 fastq.gz 7.4 GB
EGAF50000451711 fastq.gz 7.6 GB
EGAF50000451712 fastq.gz 3.3 GB
EGAF50000451713 fastq.gz 3.4 GB
EGAF50000451714 fastq.gz 6.3 GB
EGAF50000451715 fastq.gz 6.4 GB
EGAF50000451716 fastq.gz 6.3 GB
EGAF50000451717 fastq.gz 6.3 GB
EGAF50000451718 fastq.gz 3.2 GB
EGAF50000451719 fastq.gz 3.2 GB
EGAF50000451720 fastq.gz 3.2 GB
EGAF50000451721 fastq.gz 3.2 GB
EGAF50000451722 fastq.gz 4.6 GB
EGAF50000451723 fastq.gz 4.6 GB
16 Files (81.9 GB)