Illumina genome sequencing data for HICF2 craniosynostosis families (Genome Medicine)
BAM files for two families recruited to the HICF2 genome sequencing project due to craniosynostosis. One family is a singleton and the other is an affected mother-daughter duo.
- 3 samples
- DAC: EGAC00001003438
- Technologies: Illumina HiSeq 2500, Illumina HiSeq 4000
Genetic Basis of Craniofacial Malformations Protocol (London-Riverside REC;09/H0706/20)
Genetic Basis of Craniofacial Malformations data access policy The individual(s) have agreed that their de-identified research data may be deposited in managed databases where it can be accessed on request by other investigators undertaking approved research, in both the public and private sectors, in the UK and internationally. To assist the DAC, we therefore request that applicants provide i) a brief description of the research question being addressed, ii) any associated REC approval, and iii) confirm that they will not try to identify any individual(s).
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 |
|---|---|---|
| EGAS00001007575 | Whole Genome Sequencing |