Helping Children, Together
If you know of a child that may benefit from being part of Genomes in Need, please let us know by submitting a Support Request.
Genomes In Need enables genetic researchers, bioinformaticians and the global community to work together to analyze the genomes of children with severe, undiagnosed diseases.
Genomes In Need focuses on babies and children that suffer from an unknown disease that gets worse each day. Fortunately, there is hope.
When the genetic cause of the disease has been identified, doctors have been able to implement life-saving treatments and even cures for some of the children.1,2,3,4 Time is therefore of the essence in identifying the genetic cause of their disease.
Working together, we can solve these medical mysteries and provide hope for these children.
Participating in Genomes in Need is entirely free. All information and knowledge contributed to Genomes In Need are open source and publically available to all.
All data and information, including medical reports, are de-identified so that the child and the family remain anonymous.
Genomes in Need is sponsored by Sequencing.com.
1Genome (2015) Diagnosis Unknown
2MedScape (2013) Cutting-Edge DNA Sequencing Used to Diagnose Unknown Disease
3Forbes (2011) The First Child Saved By DNA Sequencing
4Science Daily (2010) Genetic sequencing used to identify and treat unknown disease