Genomics

Dataset Information

0

HipSci RNASEQ Usher syndrome and congenital eye defects

ABSTRACT: The HipSci project brings together diverse constituents in genomics, proteomics, cell biology and clinical genetics to create a UK national iPS cell resource and use it to carry out cellular genetic studies. In this sub-study we perform RNAseq on iPS lines from Usher syndrome and congenital eye defects.

PROVIDER: EGAS00001001997 | EGA |

REPOSITORIES: EGA

Json Xml

Similar Datasets

Genomics HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
| EGAS00001002008 | EGA
Genomics HipSci Whole Exome sequencing Usher syndrome and congenital eye defects
| EGAS00001001985 | EGA
Genomics HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
| EGAS00001002023 | EGA
Transcriptomics HipSci Illumina 450K Methylation analysis _open access data for healthy volunteers
2015-11-16 | E-MTAB-4059 | biostudies-arrayexpress
Transcriptomics HipSci HumanHT 12v4 Expression BeadChip analysis _open access data for healthy volunteers
2015-11-16 | E-MTAB-4057 | biostudies-arrayexpress
Genomics HipSci RNASEQ Congenital hyperinsulinia
| EGAS00001001988 | EGA
Genomics HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
| EGAS00001002010 | EGA
Genomics HipSci Whole Exome sequencing Congenital hyperinsulinia
| EGAS00001001977 | EGA
Transcriptomics RNA-seq of coding RNA in human fibroblasts, PBMCs and induced pluripotent stem cells (iPS cells) as part of the HipSci project
2016-06-22 | E-MTAB-4748 | biostudies-arrayexpress
Genomics HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
| EGAS00001002025 | EGA