Laboratory Services offered by
Department of Hematology
PGIMER Research A Block (Anand Building), Fifth Floor
Blood and Marrow morphology (Room No. H-12)
Bone marrow aspiration and trephine biopsy
Bone marrow/ blood cell cytochemistry
Complete blood count (CBC)/(hemogram/smear/reticulocyte count etc.)
Erythrocyte sedimentation rate (ESR)
Immunohistochemistry (per antibody)
Peripheral smear (blood film morphology)
Body fluid analysis (Room No. 125, New OPD and Room No. 24, EMOPD, Nehru Hospital)
CSF cell count and microscopic examination
Urine chemistry
Urine microscopy
Coagulation (Room No. H-7)
ADAMTS-13 activity assay by CLIA
Anti Beta 2 glycoprotein-1 (GP1)
Anti cardiolipin antibody
Anti-thrombin-III assay
Anti Xa assay for heparin
Coagulation screen-PT APTT fibrinogen
Correction studies in coagulation
D-dimer assay quantitative
Factor ii assay
Factor inhibitor
Factor ix assay
Factor v assay
Factor vii assay
Factor viii assay
Factor x assay
Factor xi assay
Factor xiii antigen assay
Fibrinogen assay
Flow cytometric assay for platelet function disorders
Hemophilia – DNA diagnosis
Inhibitor screen
INR
Lupus anticoagulant
Platelet function test/ platelet aggregation studies
Platelets associated antibody
Protein C
Protein S
Prothrombin time
PTTK/APTT
Ristocetin cofactor activity (RICOF)
Screening of heparin induced thrombocytopenia antibody (HIT-IGG) assay
Von willebrand antigen assay (VWF antigen)
Von willebrand factor- collagen binding assay
Cytogenetics (Room No. H-9)
Chromosomal breakage studies from peripheral blood
FISH panel i for Hematology-single probe
FISH panel ii for Hematology-two/ three probe
FISH panel iii for Hematology- four or more probes or on sorted cells
Flow Cytometry (Room No. H-4)
Extended panel per monoclonal instead of flow cytometric immunophenotyping individual monoclonal antibody
Flow cytometric assay for minimal residual disease
Flow cytometric assay for paroxysmal nocturnal hemoglobinuria (PNH)
Flow cytometric ema dye binding assay for hereditary spherocytosis
Flow cytometric enumeration of hematopoietic stem cells
Flow cytometric immunophenotyping for leukemia/lymphoma
Flow cytometric osmotic fragility test
Flow cytometric test for G6PD deficiency
Flow cytometry for DNA index
Flow cytometry for platelet function defect
Hemolytic and Nutritional Anemia (Room No. H-16)
Auto haemolysis
Coombs’ test
Foetal haemoglobin
G6PD enzyme activity assay
G6PD screening test
Ham’s test
Heinz bodies
Hemoglobin electrophoresis and high performance liquid chromatography
Incubated osmotic fragility (RBC)
Iron profile including Ferritin, Serum iron, TIBC
Met-haemoglobin estimation
Nutritional anemia profile: Serum Iron, TIBC, Transferrin saturation, Ferritin, B12 and Folate assay
Osmotic fragility (RBC)
Presumptive test of hemolysis (plasma hemoglobin)
Presumptive test of hemolysis (urine hemoglobin)
Reticulocyte count
Screening for thalassemias & hemoglobinopathies by HPLC
Sickling test
Sucrose lysis test
Unstable hemoglobins
Urine hemosiderin
Molecular Hematology (Room No. H-10/H-14)
Antenatal diagnosis of Hemoglobinopathies(e.g. Thalassemia) and inherited bleeding disorders (e.g. Hemophilia )
Chimerism analysis by DNA sequencer
Copy number variation by MLPA
Digital droplet PCR testing
DNA-based mutation detection in thalassemia
DNA-based mutation testing for single gene disorders
DNA-based mutation testing in leukemia (per mutation)
Fragment analysis for single gene mutation
Fragment analysis for two gene mutation
IGHV gene mutation status
Immunoglobulin receptor clonality analysis
Lineage specific chimerism by DNA sequencer
Microarray high sensitivity
Microarray medium sensitivity
Molecular testing by real time quantitative PCR (rq-PCR) in leukemia
Molecular testing by reverse transcriptase PCR (rt-PCR) in leukemia
Next generation sequencing for hematological disorders
Sanger sequencing 2-4 reaction bidirectional
Sanger sequencing 5-10 reaction bidirectional
Sanger sequencing single reaction bidirectional
TCR gene rearrangement