Illumina short-reads and 10X Genomics linked-reads sequencing data for MCF7 and a primary breast tumor sample
This dataset contains whole genome sequencing data from Illumina short-reads sequencing (2X150bp) and 10X Genomics linked-reads sequencing. Both the sequencing technologies were used to sequence MCF7 cell line and a primary breast triple-negative cancer sample. The fastq of paired-end reads for both the samples sequenced with both the technologies is available.
- 4 samples
- DAC: EGAC00001001424
- Technology: Illumina NovaSeq 6000
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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 |
---|---|---|
EGAS00001004093 | Other |
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 | |
---|---|---|---|---|
EGAF00003038264 | fastq.gz | 47.6 GB | ||
EGAF00003038265 | fastq.gz | 50.1 GB | ||
EGAF00003038266 | fastq.gz | 81.3 GB | ||
EGAF00003038267 | fastq.gz | 86.0 GB | ||
EGAF00003038268 | fastq.gz | 13.9 GB | ||
EGAF00003038269 | fastq.gz | 14.5 GB | ||
EGAF00003038270 | fastq.gz | 14.4 GB | ||
EGAF00003038271 | fastq.gz | 14.9 GB | ||
8 Files (322.6 GB) |