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Exome Sequencing for brazilian patients with Idiopathic Collapsing Glomerulopathy

This dataset contains 2 BAM files sequenced with Illumina NextSeq 500 e NovaSeq 600 and 20 files with variant calling sequenced with Illumina NextSeq 500 e NovaSeq 600.

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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
EGAS50000000064 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 Located in
EGAF50000054750 dedup-001 9.3 GB
EGAF50000054751 dedup-002 286.8 MB
EGAF50000054752 GRCh38 12.1 MB
EGAF50000054753 GRCh38 12.3 MB
EGAF50000054754 GRCh38 12.1 MB
EGAF50000054755 GRCh38 11.2 MB
EGAF50000054756 GRCh38 12.0 MB
EGAF50000054757 GRCh38 11.4 MB
EGAF50000054758 GRCh38 11.6 MB
EGAF50000054759 GRCh38 11.5 MB
EGAF50000054760 GRCh38 12.7 MB
EGAF50000054761 GRCh38 3.5 MB
EGAF50000054762 GRCh38 12.4 MB
EGAF50000054763 GRCh38 11.8 MB
EGAF50000054764 GRCh38 12.5 MB
EGAF50000054765 GRCh38 12.2 MB
EGAF50000054766 GRCh38 12.5 MB
EGAF50000054767 GRCh38 11.8 MB
EGAF50000054768 GRCh38 11.8 MB
EGAF50000054769 GRCh38 11.2 MB
EGAF50000054770 GRCh38 12.6 MB
EGAF50000054771 GRCh38 11.0 MB
22 Files (9.8 GB)