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Primary Lung Cancer whole genome study

Genomic libraries (500 bps) will be generated from total genomic DNA derived from lung cancer patients and subjected to short paired end sequencing on the llumina platform. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.

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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
EGAS00001000354 Cancer Genomics

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
EGAF00000156235 bam 24.0 GB
EGAF00000156236 bam 21.9 GB
EGAF00000156237 bam 16.9 GB
EGAF00000156238 bam 26.8 GB
EGAF00000162423 bam 20.8 GB
EGAF00000164121 bam 30.0 GB
EGAF00000164122 bam 33.7 GB
EGAF00000164123 bam 34.5 GB
EGAF00000164124 bam 34.5 GB
EGAF00000164125 bam 37.7 GB
EGAF00000167239 bam 33.1 GB
EGAF00000188425 bam 15.4 GB
EGAF00000188426 bam 12.4 GB
EGAF00000188427 bam 11.6 GB
EGAF00000188428 bam 12.8 GB
EGAF00000234398 bam 31.6 GB
EGAF00000234399 bam 32.8 GB
EGAF00000234400 bam 33.1 GB
EGAF00000234401 bam 30.6 GB
EGAF00000234402 bam 30.7 GB
EGAF00000234403 bam 37.4 GB
EGAF00000278984 bam 32.0 GB
22 Files (594.1 GB)