At a glance services by Genetics solutions Bangladesh

  • Primary metabolic disorders (Ammonia, Lactate, Urinary ketone bodies, ABG (Arterial blood Gas)
  • Metabolic disorder / Newborns Screening / IMD panels (Inborn metabolic disorders) / IEM’s (Inborn errors of metabolism) / TMS (Tandem Mass spectrometry)
  • Urinary CMV DNA quantitative by pcr
  • Amino acid quantitative (HPLC; high performance liquid chromatography)
  • Urinary organic acid / GCMS (Gas chromatography Mass spectrometry)
  • Cytogenetic (Blood, Bone marrow, POC/ Abortus materials, CVS/chorionic villus sampling, AF/Amniotic fluid, Cord Blood
  • FISH (Florescence in Situ Hybridization)
  • Microdeletion syndrome
  • FISH for Leukemia’s / Cancer
  • IHC / Immunohistrychemistry (More than 100 IHC can be done)Microarrays
  • Molecular tests (Pcr, rt-pcr & Sanger sequencing)
  • Infections disease (many bacterial & viral DNA, RNA; qualitative & quantitative including genotyping)
  • Biochemical tests
  • HLA & Immunogenic tests
  • MLPA (); deletion/ duplication
  • Sanger Sequencing (Single or double gene)
  • NIPT (Noninvasive prenatal testing)
  • Liquid biopsy
  • NGS (Next Generation Sequencing)
  • Genetic Tests (Single gene, Panel gene & disease wise gene)
  • Prenatal Diagnosis (40 genetic disease can be done in prenatally from CVS & AF if gene defect known)