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Deep sequencing analysis of human iPSC-specific SNVs in donor cell population

CR products were obtained from each target loci using genomic DNA from human iPS cells. Subsequently, PCR products are pooled and subjected to Illumina library preparation. The library will be sequenced either by HiSeq or MiSeq. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see

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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
EGAS00001000373 Resequencing

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
EGAF00000163182 bam 613.7 MB
EGAF00000163183 bam 257.1 MB
EGAF00000163184 bam 1.1 GB
EGAF00000163185 bam 460.1 MB
EGAF00000163186 bam 1.1 GB
EGAF00000163187 bam 454.6 MB
EGAF00000163263 bam 1.1 GB
EGAF00000163264 bam 439.0 MB
EGAF00000163265 bam 263.9 MB
EGAF00000163266 bam 278.0 MB
EGAF00000163267 bam 284.9 MB
EGAF00000163268 bam 233.9 MB
EGAF00000163269 bam 177.9 MB
EGAF00000163270 bam 145.9 MB
EGAF00000164212 bam 410.0 MB
EGAF00000164213 bam 432.7 MB
EGAF00000164214 bam 439.7 MB
EGAF00000164215 bam 362.7 MB
EGAF00000164216 bam 282.3 MB
EGAF00000164217 bam 229.4 MB
EGAF00000166817 bam 13.2 GB
EGAF00000166818 bam 5.8 GB
EGAF00000167250 bam 11.3 GB
EGAF00000167251 bam 5.0 GB
24 Files (44.4 GB)