4 - transcriptome (.bam) files, 2 -called somatic mutations (.vcf) files and 2 coverage (.csv) files
The dataset contains 4 .bam whole transcriptome files that were generated from 2 tumor samples (one .bam file per sample was created using exome-capture (hybrid capture) and the other .bam file was created using ribo-repletion (inverse mRNA selection) library preparation technology). The dataset also contains 2 somatic mutations (.vcf - sample) files (one per sample) which serve as input for Vardetector package (vardetector/vardetector at main · julijselb/vardetector) to produce somatic coverage over those mutations from the .bam file. Therefore, the dataset also contains 4- .csv files (number of reads per somatic mutation that contain the somatic mutation variant and the ones that do not contain the somatic mutation variant) that serve as outputs of the Vardetector package.
- 02/12/2025
- 4 samples
- DAC: EGAC50000000820
- Technology: Illumina NovaSeq X
DUO:0000006 version: 2021-02-23
health or medical or biomedical research
This data use permission indicates that use is allowed for health/medical/biomedical purposes; does not include the study of population origins or ancestry.
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:0000021 version: 2021-02-23
ethics approval required
This data use modifier indicates that the requestor must provide documentation of local IRB/ERB approval.
DUO:0000024 version: 2021-02-23
publication moratorium
This data use modifier indicates that requestor agrees not to publish results of studies until a specific date.
DUO:0000028 version: 2021-02-23
institution specific restriction
This data use modifier indicates that use is limited to use within an approved institution.
UCG Institutional approval policy
To obtain the data, the Golnik University Clinic Institutional Review Board must approve the request, regarding the potential data usage and the compliance of usage with ethics guidelines
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 |
|---|---|---|
| EGAS50000001419 | Transcriptome Analysis |
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
i
|
|---|---|---|---|---|
| EGAF50000499895 | csv | 274.6 kB |
|
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| EGAF50000499896 | bam | 3.5 GB |
|
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| EGAF50000499897 | csv | 355.4 kB |
|
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| EGAF50000499898 | bam | 4.7 GB |
|
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| EGAF50000499899 | vcf | 6.8 MB |
|
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| EGAF50000499900 | csv | 237.3 kB |
|
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| EGAF50000499901 | bam | 3.1 GB |
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| EGAF50000499902 | csv | 407.8 kB |
|
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| EGAF50000499903 | bam | 5.2 GB |
|
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| EGAF50000499904 | vcf | 8.2 MB |
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| 10 Files (16.5 GB) | ||||
