The Genome Foundation has a rich portfolio of services on offer. We continue to innovate to expand the breadth & depth of our offerings whilst expanding the reach of these services to the underserved corners of India. The current services on offer include:

  • Diagnostic services for
    • Genetic disorders
    • Infectious Diseases and Cancer
    • DNA Fingerprinting (Civil, Forensic, Agriculture, Wild Life, etc)
  • Regenerative Medicine (Stem cell technology)
  • Training in Medical Biotechnology & Bioinformatics
  • Public awareness and Mass Education

MOLECULAR DIAGNOSTIC SERVICES PROVIDED AT GENOME FOUNDATION
Test / Panel Test subset Reporting Time
Beta thalassemia (HBB gene) a. whole gene sequencing 2weeks
  b. single mutation screening as per doctor’s request 2weeks
  c. screening of seven common mutation 2weeks
Sickle cell Anemia (HbS mutation)   2weeks
Duchenne Muscular Dystrophy a. 24 exon screening(deletion/duplication) 2weeks
  b. deletion/duplication screening of 79 exons 2weeks
  c. carrier analysis 2weeks
Spinal Muscular Atrophy a. exon 7 & 8 deletion screening 2weeks
  b.carrier analysis 2weeks
Mitochondrial gene Mutation a. LHONs disease 2weeks
  b. Leighs disease 2weeks
  c. Mutation screening as per doctor’s request 2weeks
CFTR gene a. Four common mutation 3 weeks
  b. Delta 508 mutation 2weeks
MTHFR gene a.1298A>C 2weeks
  b.677C>T 2weeks
Huntington’s Disease   2weeks
CAG repeats in Androgen Receptor
genefor Baldness
  2weeks
Non-SyndromicHearing Loss (NSHL)
(GJB2) exon2 screening
  2weeks
DNA Finger printing   2weeks
Cardiomyopathy MYBPC3 Gene-25 base pair deletion 2weeks
Prenatal sample testing+ Maternal
cell contamination check
  2 weeks
DNA isolation   1 week
Congenital Glaucoma   2 weeks
     
KARYOTYPING AND FISH SERVICES PROVIDED AT GENOME FOUNDATION
Tests done with Karyotyping Nature of specimen Reporting time
1.Trisomy18, 13, 21 Peripheral Blood 2 weeks
2.Males with extra Y    
3.TURNERS SYNDROME    
4.XY females    
5. Testsdone with FISH MULTI COLOURPROBE FOR 18, X,Y & 13, 21 3 days
  •Quick Detection of Trisomies(13,18,21)
using interphasenuclei.
 
  •Aneuploidiesinvolving X, Y chromosome  
  Chromosomal Translocations(BCR-ABL)  
     

*Other probes related to Haematological Cancer / other disorders will be acquired as per request from Physicians/ Surgeons

 

For further details, please see attached or visit our diagnostic center at Prasad Hospitals, Nacharam, Hyderabad (Map Link),

Email: genomefoundation@gmail.com 

Tel: Mr Gaurav Gupta: +91 78427 80533 or Dr Lalji Singh: +91 98480 37558

 

 

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