Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician | DNA Labs India Medical Team
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician
MBBS, MD (General Medicine)
🏅 Reg. No: 8052
Credentials
MBBS, MD (General Medicine)
Recognized By
Karnataka Medical Council
Registry Number
8052
Experience
—
Profiles
Tests Medically Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR
- 11Catecholamines Plasma Test
- 25Immunohistochemistry Single Marker with Interpretation Test
- 26Immunohistochemistry ALK-1 Test
- 3517-Hydroxy-Corticosteroids (17-OHCS) 24 Hour Urine Test
- 40SARS-CoV-2 Antibody IgG CLIA Test
- 52Acetylcholinesterase Amniotic Fluid Test
- 55Acetylcholine Receptor (AChR) Modulating Antibody Test
- 57ACTH Test
- 75AFP (Alpha Fetoprotein): Maternal Test
- 78Alkaptonuria Urine Qualitative Test
- 89Aluminium Serum Test
- 91Aluminium Dialysis Fluid Test
- 108AML ETO t(8;21) Gene Rearrangement PCR Qualitative Test
- 120ANCA-PR3 (Serine Proteinase 3 Antibodies) EIA Test
- 122Andrology Panel Test
- 125Anemia Panel 1 Test
- 128Antenatal Panel 1 Test
- 139Anti ds DNA Antibody Crithidia IFA Test
- 140Anti IA-2 (Insulinoma Associated Antigen) Test
- 142Anti Neutrophil Cytoplasmic Antibody (ANCA) Panel Serum Test
- 145Anti NMO (Neuromyelitis Optica) Panel Serum Test
- 146Anti Nuclear Antibody / Factor (ANA / ANF) EIA Test
- 147Anti Nuclear Antibody / Factor (ANA / ANF) IFA (HEP-2) Reflex to ENA Profile Test
- 149Anti NMO (Neuromyelitis Optica) Panel CSF Test
- 152Anti Sperm Antibody Serum Test
- 159Arginase Test
- 161Anti-MOG (Myelin Oligodendrocyte Glycoprotein) CSF Test
- 163Antithrombin III Antigen Test
- 164Antiphospholipid Antibody APLA Profile Test
- 166Arsenic Random Urine Test
- 170ASCA (Anti Saccharomyces Cerevisiae Antibody) IgA Test
- 184Autoimmune Hepatitis Panel Test
- 185Autoimmune Interstitial Lung Disease (ILD) Panel Test
- 188Bacterial Meningitis Confirmatory Panel Test
- 217Bone Marrow Trephine Biopsy Panel Test
- 219Bone Marrow Examination Panel 2 Test
- 222Bordetella Pertussis Antibody IgG Test
- 223Breast Monitor Panel Test
- 228Bupropion Test
- 230C1 Esterase Inhibitor Functional (C1 Inactivator Functional) Test
- 234C1q Complement Test
- 236C3 & C4 Complement Panel Test
- 252Campylobacter Antigen Stool Test
- 254Cancer Breast Comprehensive Panel Test
- 267Cannabinoids (Delta-9-THC Metabolites) / Marijuana Screen Urine Test
- 268Carbamazepine Free Test
- 269Carcinoid Tumor Panel Test
- 271Cardiolipin Antibodies Panel IgG IgA & IgM Test
- 272Cardiolipin Antibody IgA Test
- 275Cardiolipin Antibody IgM Test
- 280Centromere Antibody Test
- 285Catecholamines Fractionated 24-Hour Urine Test
- 287Cervical Screen Test
- 289Chimerism Post-Engraftment Test
- 295Chlamydia Antigen Rapid Test
- 305Chromosome Analysis for Hematologic Malignancy Test
- 321Chromotouch Chromosome SNP Microarray Optima Products of Conception Test
- 329Clonazepam Test
- 332Coagulation Profile 2 Test
- 333Clozapine Test
- 338Coccidioides Antibody Test
- 341Cocaine & Metabolite Screen Urine Test
- 343Complement Total (CH50) Test
- 354Cortisone (Compound E) 24 Hour Urine Test
- 366C-Peptide Stimulation by Glucagon Test
- 372Cryoglobulins Qualitative Test
- 373C-Reactive Protein Cardio hsCRP Test
- 375Cryptosporidium Antigen Stool Test
- 380Culture Aerobic Miscellaneous with Gram Stain Test
- 384Culture Aerobic Sputum Test
- 389Culture AFB (Mycobacterium) Rapid with PNB Test
- 393Culture Fungus Test
- 411Culture Campylobacter Test
- 413Culture Helicobacter Pylori Test
- 425Cultured Fungus Identification Test
- 426Cultured AFB Other Than Tuberculosis (MOTT) DST for Rapid Growers Test
- 438Cultured AFB Antitubercular DST Levofloxacin Test
- 439Cultured AFB Antitubercular DST Ofloxacin Test
- 451Cultured AFB Antitubercular DST Rifampicin Test
- 458Cystic Fibrosis Mutation Detection Test
- 469Cytomegalovirus (CMV) Avidity IgG Test
- 474Cytomegalovirus Interferon Gamma Release Assay (IGRA) Test
- 477Dengue Fever NS1 Antigen Rapid Test
- 480Deep Vein Thrombosis Panel (DVT Panel) Test
- 490DHEA (Dehydroepiandrosterone) Test
- 492Diabetes Type 1 Autoimmune Profile Test
- 501Diphtheria-Pertussis-Tetanus Antibody Panel IgG Test
- 506Endomysial Antibody IgA IFA Test
- 507DRPLA (Dentatorubral-Pallidoluysian Atrophy) Gene Analysis Test
- 509Endotoxin Test
- 523Epstein Barr Virus Antibodies to Viral Capsid Antigen (VCA) IgG & IgM Test
- 529Estradiol Ultrasensitive Test
- 531Everolimus Test
- 535Factor II Functional Test
- 546Factor XI Functional Test
- 552Felbamate Test
- 553Fever Panel 2 Test
- 571FISH - CLL Panel Test
- 575FISH - EGFR Gene Amplification Test
- 577FISH - C-MYC Amplification Test
- 579FISH - Ewing Sarcoma (EWS) 22q12 (EWSR1) Rearrangement Test
- 586FISH - NSCLC (Non-Small Cell Lung Cancer) ALK1 & ROS1 Test
- 590FISH - MDS Panel - Chromosomes 5q, 7q, 8q & 20q Test
- 599FISH - RET Gene (10q11.2) Rearrangement Test
- 601FISH - Opposite Sex BMT (XX / XY) Test
- 602FISH - Prenatal Screening Panel Chromosomes 13, 18, 21, X & Y Test
- 618FISH - Monosomy 7 / del(7q31) for AML / MDS Test
- 635Galactose-1-Phosphate Quantitative Blood Test
- 639Galactosemia (Epimerase) Quantitative Blood Test
- 640Galactosemia Panel 2 Test
- 646Ganglioside GD1a Antibody IgG Test
- 648Ganglioside GM1 Antibodies IgG & IgM Test
- 661Ganglioside Antibody Profile IgM Test
- 667Glomerular Basement Membrane (GBM) Antibody IFA Test
- 675Glucagon Test
- 680Growth Hormone (GH) Test
- 696Helicobacter Pylori Antibodies Panel IgA & IgG Test
- 698Hemoglobin HPLC/Electrophoresis Test
- 702Hepatitis A Antibody (Anti-HAV) IgM Test
- 703Heparin Induced Thrombocytopenia (HIT) / Anti Platelet Factor 4-Heparin (PF4-H) IgG Quantitative Test
- 718Hepatitis C Viral Combo Test
- 729Hepatitis Delta Antibody (Anti-HDV) IgM Test
- 752Histo/ IHC/Cyto Digitization of Slides 6 to 10 Slides Test
- 756Histopathology Biopsy: Second Opinion Test
- 757Histopathology Direct Immunofluorescence (DIF) Kidney Biopsy Test
- 758Histopathology Direct Immunofluorescence (DIF) Skin / Conjunctival Biopsy Panel Test
- 762Histopathology Biopsy: Medium Specimen Test
- 765Histopathology Kidney: Biopsy Second Opinion Test
- 777HLA - AB (Class 1) Typing Test
- 793HLA - DR2 (DRB1*02) Test
- 797HLA - Narcolepsy (DRB115 DQB106:02 DQA1*01:02) Test
- 801HLA DNA High Resolution Typing - B Locus Test
- 808HLA Typing Test for Donor and Recipient
- 822HLA Pre-Transplant Workup Sensitized Recipient Panel 4 Test
- 829Homocysteine Quantitative Serum Test
- 841Hypersensitivity Pneumonitis Screen Test
- 844Hydroxyproline Plasma Test
- 850IGF - I & Growth Hormone Panel Test
- 852IGF Binding Protein-1 IGFBP-1 Test
- 858IMD Panel Quantitative Blood Test
- 860Imipramine Test
- 861Immune Complex Detection by C1q Binding Test
- 872Immunoglobulin IgE Serum Test
- 875Immunoglobulin IgG Synthesis Index & Rate Test
- 892Immunohistochemistry Digital Breast Cancer Panel 3 Test
- 893Immunohistochemistry SATB2 Test
- 894Immunohistochemistry MUC5AC Test
- 896Immunohistochemistry OLIG2 Test
- 903Immunohistochemistry Breast Cancer Panel 2 Test
- 909Immunohistochemistry 34-Beta E12 / HMW-CK Test
- 910Immunohistochemistry Ber-Ep4 (EpCAM) Test
- 933Immunohistochemistry Cytokeratin-20 (CK-20) Test
- 937Immunohistochemistry Epithelial Membrane Antigen (EMA) Test
- 940Immunohistochemistry Melan-A Test
- 959Immunohistochemistry Actin (Smooth Muscle Actin) Test
- 1004Immunohistochemistry IgA (Polyclonal) Test
- 1021Immunohistochemistry P16 Test
- 1022Immunohistochemistry MDM2 Test
- 1025Immunohistochemistry PD-L1 SP142 Test
- 1031Immunohistochemistry Progesterone Receptor (PR) Test
- 1045Immunohistochemistry TdT Test
- 1048Immunohistochemistry Thyroid Stimulating Hormone (TSH) Test
- 1073Immunophenotyping by Flow Cytometry CD38 Test
- 1083Immunophenotyping by Flow Cytometry CD8 Test
- 1098Immunotyping Serum Test
- 1100Immunohistochemistry Napsin-A Test
- 1103Infliximab Antibody Test
- 1115Insulin Antibodies Highly Sensitive Test
- 1116Infertility Screening Panel Females Test
- 1119Interleukin-6 (IL-6) Extended Panel Test
- 1124Islet Cell Antibody in Dilutions Test
- 1141Kidney Panel Extended Test
- 1146KRAS Mutation Codon 12 & 13 Test
- 1153Lead 24 Hour Urine Test
- 1160Leishmania (Kala Azar) rK-39 Antibody Serum Test
- 1161Leptospira Antibody IgG Test
- 1162Leishmania (Kala Azar) Antibody IgG Test
- 1163Leptin Test
- 1166Leptospira Antibodies Panel IgG & IgM Test
- 1176Lipoprotein Fractionation Ultracentrifugation Test
- 1192Lung Cancer Mutation Panel Test
- 1224Mercury 24 Hour Urine Test
- 1232Methotrexate Test
- 1243Minimal Residual Disease (MRD) Analysis for T-ALL Test
- 1247Mitochondrial Antibody (AMA) IFA Test
- 1251Mixing Studies - APTT with Prothrombin Time Studies Test
- 1254MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test
- 1260Multiple Sclerosis Panel 1 Test
- 1267Multiple Myeloma Comprehensive Profile Test
- 1272Myasthenia Gravis Panel Test
- 1273Mycoplasma Pneumoniae IgG & IgM Antibodies Panel Serum Test
- 1277Myelin Associated Glycoprotein-Sulfated Glucuronic Paragloboside Autoantibody (MAG-SGPG) IgM Test
- 1280Myositis Profile Extended IgG: 16 Antigens Test
- 1291Neuronal (Paraneoplastic) Autoantibodies Profile Advanced Test
- 1293Neuronal (Paraneoplastic) Autoantibodies Profile Test
- 1299Newborn Screening Panel 5 Test
- 1306Niemann Pick Disease Quantitative Blood Test
- 1309Nickel 24 Hour Urine Test
- 1310Newborn Screening Panel 8 Test
- 1314Nortriptyline Test
- 1326Nx Gen Sequencing: Albinism Test
- 1350Nx Gen Sequencing: Usher Syndrome Test
- 1353Oligoclonal Bands IgG CSF & Serum Test
- 1379Orotic Acid Test
- 1384Osteoporosis Panel Test
- 1392Prolactin Serum Test
- 1406SCA-17 (Spinocerebellar Ataxia): TBP Gene Mutation Test
- 1414Serotonin (5-HT) 24 Hour Urine Test
- 1417Tacrolimus FK506 Test
- 1419Tacrolimus Genotyping (CYP3A5) Test
- 1431Testosterone Panel Total & Free Test
- 1434Tetanus Toxoid Antibody IgG Test
- 1440Testosterone Stimulation by HCG Test
- 1443Tissue Transglutaminase (tTG) Antibody IgG Test
- 1445TPMT (Thiopurine Methyl Transferase) Genotyping Test
- 1457Troponin-T High Sensitive Test
- 1525DRD5 Gene Attention Deficit-Hyperactivity Disorder NGS Genetic Test
- 1553HSPB1 Gene CMT2F NGS Genetic Test
- 1558SBF2 Gene CMT4B2 NGS Genetic Test
- 1561CC2D2A Gene COACH syndrome NGS Genetic Test
- 1573COQ2 Gene Coenzyme Q10 deficiency type 1 NGS Genetic Test
- 1593PLCB1 Gene Early infantile epileptic encephalopathy type 12 NGS Genetic Test
- 1594PIGA Gene Early infantile epileptic encephalopathy type 20 NGS Genetic Test
- 1621FXN Gene Friedreich ataxia NGS Genetic Test
- 1651TMEM67 Gene Joubert syndrome type 6 NGS Genetic Test
- 1673CACNA1S Gene Malignant hyperthermia type 5 NGS Genetic Test
- 1713ZNF674 Gene Mental retardation, X-linked type 92 NGS Genetic Test
- 1760MYOT Gene Myotilinopathy NGS Genetic Test
- 1779PARK7 Gene PARK7 Parkinson NGS Genetic Test
- 1797POLG2 Gene Progressive external ophthalmoplegia with mitochondrial deletions type 4, autosomal dominant NGS Genetic Test
- 1798SELENON Gene Rigid spine muscular dystrophy NGS Genetic Test
- 1815ENTPD1 Gene SPG64 NGS Genetic Test
- 1819CYP7B1 Gene SPG5A NGS Genetic Test
- 1845GRM1 Gene Spinocerebellar ataxia type 13, autosomal recessive NGS Genetic Test
- 1853PEX19 Gene Zellweger syndrome NGS Genetic Test
- 1921CTSD Gene Ceroid lipofuscinosis neuronal type 10 NGS Genetic Test
- 1925ABCB4 Gene Cholestasis progressive intrahepatic type 3 NGS Genetic Test
- 1962CTNS Gene Cystinosis, nephropathic NGS Genetic Test
- 1968GLYCTK Gene D-glyceric aciduria NGS Genetic Test
- 1973F2 Gene Factor II deficiency NGS Genetic Test
- 1986FANCI Gene Fanconi anemia type I NGS Genetic Test
- 1998GALE Gene Galactose epimerase deficiency NGS Genetic Test
- 2039PFKM Gene Glycogen storage disease type 7 NGS Genetic Test
- 2078APOA2 Gene Hypercholesterolemia, familial, modifier of NGS Genetic Test
- 2094HOGA1 Gene Hyperoxaluria type 3 NGS Genetic Test
- 2150HNF1A Gene Maturity-onset diabetes of the young type 3 NGS Genetic Test
- 2151CEL Gene Maturity-onset diabetes of the young type 8 NGS Genetic Test
- 2192NAGS Gene N-acetylglutamate synthase deficiency NGS Genetic Test
- 2218PSAP Gene Prosaposin deficiency NGS Genetic Test
- 2236PKLR Gene Pyruvate kinase deficiency with hemolytic anemia NGS Genetic Test
- 2250SUOX Gene Sulfite oxidase deficiency NGS Genetic Test
- 2258SFTPC Gene Surfactant metabolism dysfunction type 2 NGS Genetic Test
- 2322GIPC3 Gene Deafness, autosomal recessive type 15 NGS Genetic Test
- 2328RDX Gene Deafness, autosomal recessive type 24 NGS Genetic Test
- 2345TIMM8A Gene Opticoacoustic nerve atrophy with dementia NGS Genetic Test
- 2402LAMA3 Gene Epidermolysis bullosa, junctional, Herlitz type NGS Genetic Test
- 2408MATN3 Gene Epiphyseal dysplasia, multiple, type 5 NGS Genetic Test
- 2416NFKB2 Gene Immunodeficiency common variable type 10 NGS Genetic Test
- 2444MT-TK Gene MERRF syndrome, MT-TK related NGS Genetic Test
- 2526MYH7 Gene Cardiomyopathy, familial hypertrophic type 1 NGS Genetic Test
- 2559ACTA2 Gene Aortic aneurysm, familial thoracic type 6 NGS Genetic Test
- 2577SLC3A1 Gene Cystinuria NGS Genetic Test
- 2589F12 Gene Factor XII deficiency NGS Genetic Test
- 2601SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test
- 2622NPHS1 Gene Nephrosis, Finnish type NGS Genetic Test
- 2631LEP Gene Obesity due to leptin deficiency NGS Genetic Test
- 2654SECISBP2 Gene Thyroid hormone metabolism abnormal NGS Genetic Test
- 2655P2RY12 Gene Bleeding disorder, platelet-type 8 NGS Genetic Test
- 2657ACTN1 Gene Bleeding disorder, platelet-type 15 NGS Genetic Test
- 2660HBB Gene Delta-beta thalassemia NGS Genetic Test
- 2661HBG2 Gene Cyanosis, transient neonatal NGS Genetic Test
- 2663RPS26 Gene Diamond-Blackfan anemia type 10 NGS Genetic Test
- 2664RPL15 Gene Diamond-Blackfan anemia type 12 NGS Genetic Test
- 2695JAK2 Gene Thrombocytosis, familial, JAK2 related NGS Genetic Test
- 2709HSD17B4 Gene D-bifunctional protein deficiency NGS Genetic Test
- 2752TLR5 Gene Legionnaire disease, susceptibility to NGS Genetic Test
- 2767CEP135 Gene Microcephaly, autosomal recessive type 8 NGS Genetic Test
- 2771STIL Gene Microcephaly, autosomal recessive type 7 NGS Genetic Test
- 2778YWHAE Gene Miller Dieker lissencephaly syndrome NGS Genetic Test
- 2806EMX2 Gene Schizencephaly NGS Genetic Test
- 2809HESX1 Gene Septooptic dysplasia NGS Genetic Test
- 2815TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly NGS Genetic Test
- 2834SUFU Gene Basal cell nevus syndrome NGS Genetic Test
- 2876ANTXR1 Gene Hemangioma capillary infantile NGS Genetic Test
- 2884RUNX1 Gene Leukemia, acute myeloid NGS Genetic Test
- 2890MC1R Gene Melanoma, cutaneous malignant NGS Genetic Test
- 2894MITF Gene Melanoma, cutaneous malignant NGS Genetic Test
- 2918PALB2 Gene Pancreatic cancer type 3, susceptibility to NGS Genetic Test
- 2933AAAS Full Gene Sequence Analysis (Allogrove Syndrome)
- 2943ALL PCR Panel Cytogenetics + PCR (BCR/ABL,TEL/AML1,MLL, E2A]
- 2945Bone Marrow for Karyotyping
- 2951Bone Marrow Aspirate Morphology
- 2970cKIT Mutation Screening (Exons 9, 11, 13, 17) AML
- 2986Cytochrome P450 2D6 Genotyping (CYP2D6 - Alleles)
- 2988Criggler Najjar Syndrome
- 2992Fetal Blood For Karyotyping
- 2996Epstein Barr Virus Qualitative PCR
- 3023Hb Electrophoresis by HPLC
- 3036Herpes Simplex Virus Type 1 & Type 2 (HSV 1 & 2) Qualitative PCR
- 3044Huntington Disease (HD) Mutation Screening
- 3061Inv(16) (AML M4Eo)
- 3079Methylenetetrahydrofolate Reductase (MTHFR), Factor V (F5), Factor II (F2)
- 3081m-FISH
- 3094Microcephaly Gene Panel
- 3102Myeloproliferative Leukemia Mutation Screening (MPL - S505N; W515L)
- 3103MYD88 Gene Mutation Analysis
- 3105Myeloproliferative Neoplasia (MPN) Panel (BCR QLT,JAK2 PANEL,CALR, MPL)
- 3108MYEOV/IgH (MM)
- 3122NTRK3
- 3125Oncomine Comprehensive Assay
- 3134Pancreatic Mutation Panel
- 3147Peripheral Blood for Karyotyping (Single)
- 3148Peripheral Blood for High Resolution Couple Karyotyping
- 3150Plasmacytosis
- 3151PML/RARA Qualitative [BCR 1 & 3]
- 3152PML/RARA (AML - M3 [APML])
- 3160Prader-Willi Syndrome (Karyotyping + FISH)
- 3165Prenatal Diagnostic Screening by Karyotyping
- 3170QF PCR [Any One Marker]+ Karyotyping
- 3176Quadruple Marker
- 3179RET (NSCLC)
- 3185Review of 10-15 Slide and Block
- 3203Small Biopsy Bottle No 6
- 3208Small Biopsy Bottle No 9
- 3212Spino Cerebral Ataxia (SCA - Single Form)
- 3214Synovial Sarcoma [SS18]
- 3218Targeted Mutation Analysis (More Than 2 Mutations)
- 3227TORCH Panel Real Time PCR
- 3231VNTR Chimerism Study [POST-BMT]
- 3237Warfarin Therapeutic Response Predictive Assay (VKORC1 & CYP2C9)
- 3245Clinical Exome Next Generation Sequencing Test
- 3246Pregnancy Non-Invasive Prenatal NIPT Test
- 3252BAS Congo Virus Viral Load Quantitative Test
- 3256Beta-Actin Quantitative Test
- 3259BCR/ABL Major Quantitative Test
- 3272Campylobacter Jejuni (RNA Detection) Qualitative Test
- 3312Hepatitis A Virus (HAV) Viral Load Quantitative Test
- 3313Hepatitis A Virus (HAV) (RNA Detection) Qualitative Test
- 3326HSV 1 & 2 Viral Load Quantitative Test
- 3348Streptococcus Mutans Bacterial Load Test
- 3360Treponema Palladium (Syphilis) Bacterial Load Test
- 3362TNF (RNA Detection) Qualitative Test
- 3370Celery Allergen Test
- 3371Fish Allergen Test
- 3373Soy Allergen Test
- 3374Walnut / Pecan Allergen Test
- 3392Wheat GMO Testing
- 3403MeDIP Sequencing
- 3408Targeted Sequencing- Below 50 Kb
- 3415RNA Viral Metagenome Sequencing
- 3429Bacterial Transcriptome Library Preparation
- 3443Rabies Antibody Test for human
- 3450Longevity Epigenetic DNA Methylation Biological Age BioAge DNA Test
- 3464Autogen Plus Panel Test
- 3475HLA - B15 (B*15) Test
- 3485IBD (Inflammatory Bowel Disease) Screening Panel Test
- 3487HLA Pre-Transplant Workup Sensitized Recipient Panel 5 Test
- 3491Immunophenotyping by Flow Cytometry CD2 Test
- 3502Immunophenotyping by Flow Cytometry: Leukemia Monitoring Panel-Hairy Cell Test
- 3509Interleukin-6 (IL-6) Mini Panel Test
- 3518Ovarian Cancer Panel Test
- 3520Oxalate 24 Hour Urine Test
- 3525Parietal Cell Antibody IFA in Dilutions Test
- 3529Parvovirus B19 Antibody IgM Test
- 3531Parietal Cell Antibody IFA Test
- 3533Peritoneal Equilibrium Test (PET) Test
- 3541Phenol Test
- 3544Phosphatidylserine Antibodies Panel IgG & IgM Test
- 3548Phosphatidylserine Antibody IgG Test
- 3550Phosphatidylserine Antibody IgM Test
- 3552Phospholipid Antibody IgG Test
- 3554Phospholipid Antibody IgM Test
- 3555Pigeon Feathers IgE Test
- 3556PIK3CA Mutation Analysis Test
- 3561Plasminogen Activator Inhibitor-1/SERPINE-1 4G/5G Genotyping Test
- 3584Prothrombin Time Studies Test
- 3586Purkinje Cell Cytoplasmic Antibody Type Tr (DNER) Test
- 3587Respiratory Comprehensive Panel Test
- 3600Rett Syndrome Detection Test
- 3601Respiratory Panel 4 Test
- 3602Rheumatoid Factor IgA Test
- 3609Reticulin IgA Antibody Test
- 3611Rubella (German Measles) Antibodies Panel IgG & IgM Test
- 3614Rubella (German Measles) Antibody IgM Test
- 3616SARS-CoV-2 Antibodies Profile Test
- 3619Rubella IgG Advantage Test
- 3627SCA (Spinocerebellar Ataxia) Profile: Any 4 Markers Test
- 3636SCA-14 (Spinocerebellar Ataxia): PRKCG Gene Mutation Test
- 3648Sm/RNP Antibody Test
- 3652Smooth Muscle Antibody (ASMA) IFA in Dilutions Test
- 3654Sperm DNA Fragmentation DFI Test
- 3673Striated/Skeletal Muscle Antibody (ASKA) IFA Test
- 3680TB Platinum Interferon Gamma Release Assay (IGRA) Test
- 3683Testosterone Free Test
- 3716Tumor Necrosis Factor (TNF) Alpha Test
- 3719U1RNP Antibodies Test
- 3724Vasculitis Panel Test
- 3727Varicella Zoster Virus (VZV) Qualitative PCR Test
- 3733Vitamin B12 Binding Capacity Unsaturated Transcobalamin Test
- 3736Vitamin B12 Cyanocobalamin Test
- 3754Von Willebrand Factor Ristocetin Cofactor Activity (vWF) Test
- 3765SLC45A2 Gene Albinism, Oculocutaneous Type 4 NGS Genetic Test
- 3779CRYBB3 Gene Cataract, Autosomal Recessive Congenital Nuclear Type 2 NGS Genetic Test
- 3785FYCO1 Gene Cataract, Autosomal Recessive Congenital Type 2 NGS Genetic Test
- 3792SORD Gene Cataract, Congenital NGS Genetic Test
- 3795NHS Gene Cataract, X-Linked NGS Genetic Test
- 3800ACO2 Gene Cerebellar-Retinal Degeneration, Infantile NGS Genetic Test
- 3803PAX6 Gene Coloboma, Ocular, Autosomal Dominant NGS Genetic Test
- 3808YAP1 Gene Coloboma, Ocular, with or without Hearing Impairment, Cleft Lip/Palate, and/or Mental Retardation NGS Genetic Test
- 3811RPGRIP1 Gene Cone-Rod Dystrophy Type 13 NGS Genetic Test
- 3820C21ORF2 Gene Cone-Rod Dystrophy, C21ORF2 Related NGS Genetic Test
- 3823CACNA1F Gene Cone-Rod Dystrophy, X-Linked Type 3 NGS Genetic Test
- 3838LTBP2 Gene Glaucoma, Primary Type 3D NGS Genetic Test
- 3845RB1 Gene Hereditary Retinoblastoma NGS Genetic Test
- 3864ATP1A3 Gene Alternating Hemiplegia of Childhood Type 2 NGS Genetic Test
- 3865NOS3 Gene Alzheimer Disease Type 1 NGS Genetic Test
- 3869RTN3 Gene Alzheimers Disease, RTN3 Related NGS Genetic Test
- 3877GSN Gene Amyloidosis, Finnish Type NGS Genetic Test
- 3885ANG Gene Amyotrophic Lateral Sclerosis Type 9 NGS Genetic Test
- 3890FUS Gene Amyotrophic Lateral Sclerosis Type 6 NGS Genetic Test
- 3914PTCHD1 Gene Autism Susceptibility, X-Linked Type 4 NGS Genetic Test
- 3942F5 Gene Budd-Chiari Syndrome NGS Genetic Test
- 3946PHOX2B Gene Central Hypoventilation Syndrome with or without Hirschsprung Disease NGS Genetic Test
- 3950NSDHL Gene CHILD Syndrome NGS Genetic Test
- 3952CIZ1 Gene Cervical Dystonia NGS Genetic Test
- 3959LITAF Gene CMT1C NGS Genetic Test
- 3962LRSAM1 Gene CMT2P NGS Genetic Test
- 3965MPZ Gene CMT4E NGS Genetic Test
- 3969PRX Gene CMT4F NGS Genetic Test
- 3978KARS1 Gene CMTRIB NGS Genetic Test
- 3979TUBB3 Gene Cortical dysplasia, complex, with other brain malformations, type 1 NGS Genetic Test
- 3982TUBB2A Gene Cortical dysplasia, complex, with other brain malformations, type 5 NGS Genetic Test
- 3987PRNP Gene Creutzfeldt-Jakob disease NGS Genetic Test
- 3991MT-CO2 Gene Cytochrome c oxidase 2 deficiency NGS Genetic Test
- 3998MAPT Gene Dementia, frontotemporal NGS Genetic Test
- 4000ITM2B Gene Dementia, familial, Danish type NGS Genetic Test
- 4001PSEN1 Gene Dementia, frontotemporal NGS Genetic Test
- 4005OCRL Gene Dent disease type 2 NGS Genetic Test
- 4012SCN9A Gene Dravet syndrome, modifier of NGS Genetic Test
- 4030PNKP Gene Early infantile epileptic encephalopathy type 10 NGS Genetic Test
- 4032GUF1 Gene Early infantile epileptic encephalopathy type 40 NGS Genetic Test
- 4033GRIN2D Gene Early infantile epileptic encephalopathy type 46 NGS Genetic Test
- 4035SLC2A1 Gene DYT8 NGS Genetic Test
- 4038FGF12 Gene Early infantile epileptic encephalopathy type 47 NGS Genetic Test
- 4052MT-TR Gene Encephalomyopathy, mitochondrial, MT-TR related NGS Genetic Test
- 4056BSCL2 Gene Encephalopathy, progressive, with or without lipodystrophy NGS Genetic Test
- 4068GABRA1 Gene Epilepsy, childhood absence type 4, susceptibility to NGS Genetic Test
- 4080HCN2 Gene Epilepsy, HCN2 related NGS Genetic Test
- 4087CHD2 Gene Epileptic encephalopathy, childhood-onset NGS Genetic Test
- 4097ROBO3 Gene Gaze palsy, horizontal, with progressive scoliosis NGS Genetic Test
- 4111DPAGT1 Gene Glycosylation disorder type 1J NGS Genetic Test
- 4119FLNA Gene Heterotopia, periventricular, ED variant NGS Genetic Test
- 4123WNK1 Gene HSAN2A NGS Genetic Test
- 4126ELP1 Gene HSAN3 NGS Genetic Test
- 4142GLRA1 Gene Hyperekplexia NGS Genetic Test
- 4148CACNA1S Gene Hypokalemic periodic paralysis type 1 NGS Genetic Test
- 4151DARS Gene Hypomyelination with brainstem and spinal cord involvement and leg spasticity NGS Genetic Test
- 4162GALC Gene Krabbe disease NGS Genetic Test
- 4171NDUFAF3 Gene Leigh syndrome NGS Genetic Test
- 4175NDUFS3 Gene Leigh syndrome NGS Genetic Test
- 4191PDHA1 Gene Leigh syndrome, X-linked NGS Genetic Test
- 4192HSPD1 Gene Leukodystrophy hypomyelinating type 4 NGS Genetic Test
- 4202TCAP Gene Limb-Girdle Muscular Dystrophy, autosomal recessive type 2G NGS Genetic Test
- 4206FKRP Gene Limb-girdle muscular dystrophy, autosomal recessive type 2I NGS Genetic Test
- 4209FKTN Gene Limb-girdle muscular dystrophy, autosomal recessive type 2M NGS Genetic Test
- 4211TRAPPC11 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2S NGS Genetic Test
- 4213OCRL Gene Lowe oculocerebrorenal syndrome NGS Genetic Test
- 4218KDM5C Gene Mental retardation X-linked, syndromic, Claes-Jensen type NGS Genetic Test
- 4225EPB41L1 Gene Mental retardation, autosomal dominant type 11 NGS Genetic Test
- 4226HEPACAM Gene Megalencephalic leukoencephalopathy with subcortical cysts 2A NGS Genetic Test
- 4244SYNGAP1 Gene Mental retardation, autosomal dominant type 5 NGS Genetic Test
- 4251GRIN1 Gene Mental retardation, autosomal dominant type 8 NGS Genetic Test
- 4252KIF1A Gene Mental retardation, autosomal dominant type 9 NGS Genetic Test
- 4259HERC2 Gene Mental retardation, autosomal recessive type 38 NGS Genetic Test
- 4279AP1S2 Gene Mental retardation, X-linked type 59 NGS Genetic Test
- 4280ARHGEF6 Gene Mental retardation, X-linked type 46 NGS Genetic Test
- 4281TSPAN7 Gene Mental retardation, X-linked type 58 NGS Genetic Test
- 4282RAB39B Gene Mental retardation, X-linked type 72 NGS Genetic Test
- 4285DLG3 Gene Mental retardation, X-linked type 90 NGS Genetic Test
- 4292MT-TS1 Gene MERRF/MELAS overlap syndrome, MT-TS1 related NGS Genetic Test
- 4297MT-ND4L Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4299MT-ND5 Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4300MT-ND4 Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4306NDUFAF4 Gene Mitochondrial complex I deficiency NGS Genetic Test
- 4310SDHAF1 Gene Mitochondrial complex II deficiency NGS Genetic Test
- 4315UQCRC2 Gene Mitochondrial complex III deficiency NGS Genetic Test
- 4324AKAP1 Gene Mitochondrial Disorders, AKAP1 related NGS Genetic Test
- 4327MFF Gene Mitochondrial encephalomyopathy NGS Genetic Test
- 4332PUS1 Gene Mitochondrial myopathy and sideroblastic anemia type 1 NGS Genetic Test
- 4338NFU1 Gene Multiple mitochondrial dysfunctions syndrome type 1 NGS Genetic Test
- 4347DMD Gene Muscular dystrophy, Becker type NGS Genetic Test
- 4351LMNA Gene Muscular dystrophy, congenital, LMNA related NGS Genetic Test
- 4358DMD Gene Muscular dystrophy, Duchenne type NGS Genetic Test
- 4359POMGNT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A8 NGS Genetic Test
- 4360POMT2 Gene Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2 NGS Genetic Test
- 4364DAG1 Gene Muscular dystrophy-dystroglycanopathy (limb-girdle), type C9 NGS Genetic Test
- 4365POMGNT1 Gene Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3 NGS Genetic Test
- 4368CAPN1 Gene Muscular-skeletal disorder, CAPN1 related NGS Genetic Test
- 4375DYSF Gene Myopathy, distal with anterior tibial onset NGS Genetic Test
- 4387COL6A2 Gene Myosclerosis, autosomal recessive NGS Genetic Test
- 4397MT-TV Gene Neonatal death due Leigh syndrome, MT-TV related NGS Genetic Test
- 4413ADAM22 Gene Neurodevelopmental disorder, ADAM22 related NGS Genetic Test
- 4414HSPB8 Gene Neuronopathy distal hereditary motor type 2A NGS Genetic Test
- 4415EOMES Gene Neuronal migration disorder NGS Genetic Test
- 4416IGHMBP2 Gene Neuronopathy distal hereditary motor type 6 NGS Genetic Test
- 4419PMP22 Gene Neuropathy with liability to pressure palsies [HNPP] NGS Genetic Test
- 4423POLG Gene Neuropathy with sensory ataxic, dysarthria, and ophthalmoparesis NGS Genetic Test
- 4433GNE Gene Nonaka myopathy NGS Genetic Test
- 4434NDP Gene Norrie disease NGS Genetic Test
- 4439ALX4 Gene Parietal foramina type 2 NGS Genetic Test
- 4449PLP1 Gene Pelizaeus-Merzbacher disease NGS Genetic Test
- 4453PEX3 Gene Peroxisome biogenesis disorder type 10A NGS Genetic Test
- 4459PEX1 Gene Peroxisome biogenesis disorder type 1B NGS Genetic Test
- 4472TSEN2 Gene Pontocerebellar hypoplasia type 2B NGS Genetic Test
- 4485ALS2 Gene Primary lateral sclerosis, juvenile NGS Genetic Test
- 4486NDN Gene Prader-Willi syndrome NGS Genetic Test
- 4491RUBCN Gene Salih ataxia NGS Genetic Test
- 4492RRM2B Gene Progressive external ophthalmoplegia with mitochondrial deletions type 5, autosomal dominant NGS Genetic Test
- 4493MYH7 Gene Scapuloperoneal myopathy, MYH7 related NGS Genetic Test
- 4506KCNQ3 Gene Seizures, benign neonatal, type 2 NGS Genetic Test
- 4517L1CAM Gene SPG1 NGS Genetic Test
- 4523ERLIN2 Gene SPG18 NGS Genetic Test
- 4528DDHD1 Gene SPG28 NGS Genetic Test
- 4532C19orf12 Gene SPG43 NGS Genetic Test
- 4538AP4B1 Gene SPG47 NGS Genetic Test
- 4564PPP2R2B Gene Spinocerebellar ataxia type 12, autosomal dominant NGS Genetic Test
- 4569CWF19L1 Gene Spinocerebellar ataxia type 17, autosomal recessive NGS Genetic Test
- 4602UROC1 Gene Urocanase deficiency NGS Genetic Test
- 4603CSTB Gene Unverricht-Lundborg disease NGS Genetic Test
- 4607CRPPA Gene Walker-Warburg syndrome NGS Genetic Test
- 4640ST6GAL2 Gene Beta-Galactosamide alpha-2,6-Sialyltransferase 2 deficiency NGS Genetic Test
- 4648HSD3B7 Gene Bile acid synthesis defect type 1, congenital NGS Genetic Test
- 4675FANCA Gene Fanconi anemia type A NGS Genetic Test
- 4692COG8 Gene Glycosylation disorder type 2H NGS Genetic Test
- 4713IGF1R Gene Insulin-like growth factor resistance NGS Genetic Test
- 4719L2HGDH Gene L-2-hydroxyglutaric aciduria NGS Genetic Test
- 4727SLC25A3 Gene Mitochondrial phosphate carrier deficiency NGS Genetic Test
- 4760PRPS1 Gene Deafness, X-linked type 1 NGS Genetic Test
- 4812ATP2A2 Gene Acrokeratosis verruciformis NGS Genetic Test
- 4860C1QA Gene C1q deficiency NGS Genetic Test
- 4862C5 Gene C5 deficiency NGS Genetic Test
- 4911COL3A1 Gene Ehlers-Danlos syndrome type 3 NGS Genetic Test
- 4954MLPH Gene Griscelli syndrome type 3 NGS Genetic Test
- 4982CDSN Gene Hypotrichosis type 2 NGS Genetic Test
- 4989ALOXE3 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic Test
- 4990NIPAL4 Gene Ichthyosiform erythroderma, congenital, nonbullous type 1 NGS Genetic Test
- 4999CYP4F22 Gene Ichthyosis, lamellar type 3 NGS Genetic Test
- 5020IL21R Gene Immunodeficiency, primary, autosomal recessive, IL21R-related NGS Genetic Test
- 5028PECAM1 Gene Immunological disorder, PECAM1 related NGS Genetic Test
- 5044DSG1 Gene Keratosis palmoplantaris striata type 1 NGS Genetic Test
- 5060CHRND Gene Multiple pterygium syndrome lethal type NGS Genetic Test
- 5074WNT10A Gene Odontoonychodermal dysplasia NGS Genetic Test
- 5097KRT17 Gene Pachyonychia congenita type 2 NGS Genetic Test
- 5107CSTA Gene Peeling skin syndrome type 4 NGS Genetic Test
- 5157ERCC2 Gene Trichothiodystrophy NGS Genetic Test
- 5195CACNA1C Gene Brugada syndrome type 3 NGS Genetic Test
- 5262DTNA Gene Left ventricular noncompaction 1, with or without congenital heart defects NGS Genetic Test
- 5305TRDN Gene Ventricular tachycardia, catecholaminergic polymorphic type 5 NGS Genetic Test
- 5313HTRA1 Gene CARASIL NGS Genetic Test
- 5314RASA1 Gene Capillary malformation-arteriovenous malformation NGS Genetic Test
- 5332NOS2 Gene Hypertension, susceptibility to NGS Genetic Test
- 5356Atypical hemolytic uremic syndrome Panel NGS Genetic Test
- 5373BBS12 Gene Bardet-Biedl syndrome type 12 NGS Genetic Test
- 5397INHBA Gene FSH releasing protein deficiency NGS Genetic Test
- 5399UGT1A1 Gene Gilbert syndrome NGS Genetic Test
- 5469ANKS6 Gene Nephronophthisis type 16 NGS Genetic Test
- 5485PRKCSH Gene Polycystic liver disease NGS Genetic Test
- 5488PKD2 Gene Polycystic kidney disease type 2, autosomal dominant NGS Genetic Test
- 5498SCNN1B Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic Test
- 5504BICC1 Gene Renal cystic dysplasia, cystic, susceptibility to NGS Genetic Test
- 5511CRB2 Gene Ventriculomegaly with cystic kidney disease NGS Genetic Test
- 5515LAS1L Gene Wilson-Turner syndrome NGS Genetic Test
- 5533KISS1 Gene Hypogonadotropic hypogonadism NGS Genetic Test
- 5542SOHLH1 Gene Oogenesis dysfunction NGS Genetic Test
- 5544BMP15 Gene Ovarian dysgenesis type 2 NGS Genetic Test
- 5564BTK Gene Agammaglobulinemia and isolated hormone deficiency NGS Genetic Test
- 5572ATRX Gene Alpha-thalassemia/mental retardation syndrome NGS Genetic Test
- 5575HSPA9 Gene Anemia, sideroblastic, type 4 NGS Genetic Test
- 5600KLF1 Gene Lutheran inhibitor blood group NGS Genetic Test
- 5602AMN Gene Megaloblastic anemia type 1 NGS Genetic Test
- 5611CSF3R Gene Neutrophilia, hereditary NGS Genetic Test
- 5630HBD Gene Thalassemia, delta NGS Genetic Test
- 5642DLL4 Gene Adams-Oliver syndrome type 6 NGS Genetic Test
- 5652FGFR2 Gene Apert syndrome NGS Genetic Test
- 5671UPB1 Gene Beta-ureidopropionase deficiency NGS Genetic Test
- 5677ERCC6L2 Gene Bone marrow failure syndrome type 2 NGS Genetic Test
- 5688TFAP2A Gene Branchiooculofacial syndrome NGS Genetic Test
- 5703RET Gene Central hypoventilation syndrome, congenital NGS Genetic Test
- 5722CRLF1 Gene Cold-induced sweating syndrome NGS Genetic Test
- 5738WDR19 Gene Cranioectodermal dysplasia type 4 NGS Genetic Test
- 5748ALX4 Gene Frontonasal dysplasia type 2 NGS Genetic Test
- 5753HOXA13 Gene Guttmacher syndrome NGS Genetic Test
- 5765PKD1L1 Gene Heterotaxy, visceral type 8, autosomal NGS Genetic Test
- 5769EDN3 Gene Hirschsprung disease NGS Genetic Test
- 5784FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic Test
- 5787SMN1 Gene Spinal muscular atrophy type 4 NGS Genetic Test
- 5803TTC7A Gene Intestinal atresia, multiple NGS Genetic Test
- 5805KDM6A Gene Kabuki syndrome type 2 NGS Genetic Test
- 5809FGFR1 Gene Kallmann syndrome type 2 NGS Genetic Test
- 5819KANSL1 Gene Koolen syndrome NGS Genetic Test
- 5833FBN1 Gene Marfan syndrome NGS Genetic Test
- 5835ORC1 Gene Meier-Gorlin syndrome type 1 NGS Genetic Test
- 5844MMP13 Gene Metaphyseal anadysplasia type 1 NGS Genetic Test
- 5862ALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic Test
- 5872BRAF Gene Noonan syndrome type 7 NGS Genetic Test
- 5884IRF6 Gene Orofacial cleft type 6 NGS Genetic Test
- 5887TCTN3 Gene Orofaciodigital syndrome type 4 NGS Genetic Test
- 5896LAMC1 Gene Pelvic organ prolapse, LAMC1 related NGS Genetic Test
- 5921ATR Gene Seckel syndrome type 1 NGS Genetic Test
- 5922CENPJ Gene Seckel syndrome type 4 NGS Genetic Test
- 5923CEP63 Gene Seckel syndrome type 6 NGS Genetic Test
- 5929PIK3R1 Gene SHORT syndrome NGS Genetic Test
- 5933ZBTB16 Gene Skeletal defects, genital hypoplasia, and mental retardation NGS Genetic Test
- 5936FOXP2 Gene Speech-language disorder type 1 NGS Genetic Test
- 5940NKX3-2 Gene Spondylo-megaepiphyseal-metaphyseal dysplasia NGS Genetic Test
- 5946HOXD13 Gene Syndactyly type 1 NGS Genetic Test
- 5954C12orf57 Gene Temtamy syndrome NGS Genetic Test
- 5971LRIG2 Gene Urofacial syndrome NGS Genetic Test
- 5972WNT7A Gene Ulna and fibula, absence of, with severe limb deficiency NGS Genetic Test
- 5977EPG5 Gene Vici syndrome NGS Genetic Test
- 5979FAT4 Gene Van Maldergem syndrome type 2 NGS Genetic Test
- 5986FBN1 Gene Weill-Marchesani syndrome, dominant type 2 NGS Genetic Test
- 5987WRN Gene Werner syndrome NGS Genetic Test
- 5991Breast Cancer BRCA1 BRCA2 Gene Test
- 5992CDH1 Gene Gastric cancer, hereditary diffuse NGS Genetic Test
- 5994KIT Gene Gastrointestinal stromal tumor, familial NGS Genetic Test
- 5997KRAS Gene Leukemia, acute myelogenous NGS Genetic Test
- 5999KIT Gene Leukemia, acute myeloid NGS Genetic Test
- 6001SUFU Gene Medulloblastoma, desmoplastic, familial NGS Genetic Test
- 6002CHEK2 Gene Li-Fraumeni syndrome type 2 NGS Genetic Test
- 6005RET Gene Multiple endocrine neoplasia type 2B NGS Genetic Test
- 6008PDGFRA Gene PDGFRA, selective sequencing of exons 12, 14 and 18 NGS Genetic Test
- 6010AIP Gene Pituitary adenoma, growth hormone-secreting, due to AIP germline mutation NGS Genetic Test
- 6016STAG1 Gene Prostate cancer NGS Genetic Test
- 6018ZNF783 Gene Prostate cancer NGS Genetic Test
- 6020ELAC2 Gene Prostate cancer, hereditary type 2, susceptibility to NGS Genetic Test
- 6021RET Gene RET, selective sequencing of exons 5, 8, 10, 11 and 13-16 NGS Genetic Test
- 6024SRGAP1 Gene Thyroid cancer type 2, nonmedullary, susceptibility to NGS Genetic Test
- 6026BAP1 Gene Tumor predisposition syndrome NGS Genetic Test
- 6028CYLD Gene Trichoepithelioma, multiple familial, type 1 NGS Genetic Test
- 6039Ataxia Gene Panel
- 6047Beta Thalassemia -12 Common Mutations Screening (Single)
- 6054Beta Thalassemia-HBB Full Gene Analysis (Couple)
- 6086Prenatal Delta Beta-Thalassaemia Mutation Screening
- 6089DMD Mutation Screening (79 Exons) [Prenatal]
- 6090DMD Carrier Screening (79 Exons)
- 6094DMD/BMD Mutation Screening (26 Exons) [Prenatal]
- 6105Genome Signature (HRD)
- 6107HbE (Hemoglobin E) Mutation Screening [Prenatal]
- 6131MECP2 Full Gene Mutation Analysis (RETT Syndrome)
- 6132MDS Panel (Cytogenetics + FISH [del(5q), del(7q), del(20q)])
- 6170Klebsiella Pneumonia (RNA Detection) Qualitative Test
- 6171Jak-2 Mutation Detection (RNA Detection) Qualitative Test
- 6220PML/RARA Quantitative Test
- 6238Rabies Detection RNA Qualitative PCR Test Humans
- 6249Trichomonas Vaginalis (RNA Detection) Qualitative Test
- 6260Hospital Baby Exchange Maternity DNA Test
- 6272Birds DNA Test
- 6276The Non-Invasive Prenatal (NIPT) Twins Test
- 6277FISH - Trisomy 13 / Patau Syndrome Test
- 6278FISH for X and Y
- 6279FISH - Trisomy 18 / Edward Syndrome Test
- 6282FISH for Pre or Postnatal Diagnosis Chromosome 13 21
- 6284FISH for Pre or Postnatal Diagnosis Chromosome 18, X Y
- 6286FISH for Pre or Postnatal Diagnosis Chromosome 13 22
- 6288FISH for Pre or Postnatal Diagnosis Chromosome 13 23
- 6294NIPT Advanced for 23 Chromosomes
- 6296Dog DNA Test
- 6297Whole Exome Sequencing + Chromosomal Microarray
- 6299LGMD NGS Panel
- 6300Genealogy Telomere Age Testing
- 6302Horse DNA Test
- 6304Thyroid Prognostication NGS Panel
- 6305Buffalo DNA Test
- 6311Canola / Rapeseed GMO Testing
- 6315Corn or Soy Flour, Grits, Meal, Flakes GMO Testing
- 6319DNA Extraction from Solid Tissue - Plant
- 6327DNA Extraction from Swab or Filter
- 6332DNA QC and Quantitation - Nanodrop
- 6340Bacterial Genome Sequencing, De Novo Assembly and Annotation - Illumina and ONT Hybrid
- 6341Fungal Genome Sequencing, De Novo Assembly and Annotation - Illumina
- 6342Fungal Genome Sequencing and Reference Based Analysis
- 6343Cattle Genome Sequencing and Variant Calling-30X
- 6352DNA Viral Genome Sequencing and Analysis
- 6356ChIP Sequencing and Analysis
- 6357SELEX Sequencing and Analysis
- 6364Cattle Genome Sequencing-30X
- 6377Shotgun Metagenome Sequencing Data Analysis
- 6380DNA Viral Metagenome Sequencing Data Analysis
- 6382Bacterial Genome De Novo Assembly and Annotation-Illumina
- 6383Fungal Genome Reference Based Data Analysis-Illumina
- 6384Bacterial Genome De Novo Assembly and Annotation-Illumina and ONT Hybrid
- 6395DNA Viral Genome Sequencing Data Analysis
- 6400ChIP Sequencing Data Analysis
- 6402SELEX Sequencing Data Analysis
- 6408ATAC Sequencing Data Analysis
- 6428Eukaryotic SmallRNA Sequencing and Analysis
- 6429Eukaryotic mRNA Sequencing Reference Based Data Analysis
- 6432Eukaryotic mRNA Sequencing De Novo Data Analysis
- 6434Metatranscriptome Sequencing Data Analysis
- 6435RNA Viral Metagenome Sequencing Data Analysis
- 6438Sequencing Library QC-qPCR
- 6449Comprehensive Ophthalmic Genetic Disorder Panel
- 6453Hereditary Cancer Panel
- 6455Predictive Genetic Testing for Cancer
- 6456Kardiogen Polygenic Risk Score Test
- 6457Molecular Karyotyping for Amniotic Fluid Test
Articles Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR
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