U N Mehta Institute Of Cardiology & Research Center - Gujarat
41256576 e tender for rate contract for medical laboratory blood testing outsource service (part 2) for u n mehta institute of cardiology and research centre (affiliated to b. j. medical college & nabh accredited) ahmedabad, gujarat, india. jacobsen syndrome (jbs),jak2 panel,jak2 v617f mutation by pcr,jak2 v617f mutation by sanger,jak2 v617f with reflex to exon 12,jc virus qualitative,jo 1 antibody,joubert and meckel gruber syndromes panel 18 genes,joubert syndrome (jbts) panel,juvenile polyposis syndrome bmpr1a, smad4,juvenile polyposis syndrome (jps),kabuki syndrome (kabuk) panel,kabuki syndrome panel kdm6a, kmt2d,kallmann syndrome 1 (kal1),kappa light chain,karyotype amniotic fluid,karyotype bone marrow,karyotype peripheral blood (couple),karyotype peripheral blood (husband),karyotype peripheral blood (single),karyotype products of conception,karyotype chorionic villus sampling,karyotype peripheral blood for hematological malignancy,ki 67 (ihc marker),kit and pdgfra mutation panel,kit mutations,kleefstra syndrome,klinefelter syndrome,koh examination for csf,koh preparation for fungus,koolen de vries syndrome (kdvs),krabbe disease test galc,l1 syndrome,lacosamide level,lactate level,lactate level (csf),lambda light chain,lamotrigine level,lap score,lbc pap + pcr hpv dna,lbc pap smear,ldh fluid,ldh isoenzymes,ldh serum,ldl cholesterol (direct),lead urine spot,lead level,lead level in liver biopsy,left ventricular noncompaction panel (lvnc): actc1, dsp, hcn4, lamp2, lm na, mybpc3, myh7pln, ryr2, scn5a, taz, tnni3, tnnt2, tp m1, vcl, dtna, ldb3, prdm16,lft liver function test (sgpt, sgot, billirubin total and direct, alkaline phosphatase, total protein, albumin, globulin, ag ratio),legionella igm,legionella pneumophila ag urine,legionella urinary antigen,leigh syndrome ndufs8,leigh syndrome (ls),leigh syndrome, x linked,leismania igg (ho),leismania igm (ho),leptin serum,leptospira by pcr,leptospira detection by smear examination,leptospira igg,leptospira igm,leri weill dyschondrosteosis (lwd),lesch nyhan syndrome (lns),leucocyte adhesion defect (lad),leukodystrophy, demyelinating, adult onset, autosomal dominant (adld),levetiracetam,lh,li fraumeni syndrome tp53,ligase iv syndrome test lig4,limb girdle muscular dystrophy panel 31 genes,lipase,lipase fluid,lipid profile,lipoprotein (a),liquid biopsy somatic cancer panel,liquid egfr,lissencephaly (lis) panel,lissencephaly, x linked (lisx) panel,lithium,liver profile by immunoblot,lkm 1 antibody by if,lkm antibodies elisa,loeys dietz syndrome panel smad3, tgfb2, tgfbr1, tgfbr 2, fbn1, tgfb3,long qt syndrome panel akap9, ank2, cacna1c, cav3, kcne1, kcne2, kcnh2, kcnj2, kcnj5, kcnq1, scn4b, scn5a, snta1,lowe oculocerebrorenal syndrome (ocrl),lp (a) (lipoprotein a),lubs x linked mental retardation syndrome (mrxsl),lujan syndrome test med12,lung adenocarcinoma braf,lung adenocarcinoma egfr by arms pcr,lung adenocarcinoma egfrby sanger,lung adenocarcinoma kras,lung cancer panel somatic mutations (egfr, kras, braf),lung cancer targeted gene panel (egfr kras braf met erbb2 alk1 ros1),lupus anticoagulant (la),lyme disease ( borrelia burgdorferi igm & igg ),lymphocyte subset analysis,lymphoproliferative syndrome, x linked, 1 (xlp1),lynch syndrome mlh1, msh2, msh6, pms2 (offered as single gene if there is a kfm or if there?s ihc negative staining),lynch syndrome panel epcam, mlh1, msh2, msh6, mutyh, pms2,macrocephaly/autism syndrome,magnesium,magnesium 24 hour urine,magnesium urine spot,malaria parasites,malarial antigen (rapid card) test,malignant hyperthermia susceptibility panel cacna1s, ryr1,mandibulofacial dysostosis, guion almeida type,manganese level,maple syrup urine disease panel bckdha, bckdhb, dbt,marfan syndrome (mfs),mcad common mutation analysis acadm,mdr and xdr,mdr and xdr tb rapid genotyping test,mdr tb rapid genotyping test 1st line (inh & rifampicin) lpa,mdr tb rapid genotyping test 1st line(inh and rifampicin),mds kt+fish panel (karyotyping fish del 5q del 7q del 20q cep 8),measels (rubeola) antibody igg,measels (rubeola) antibody igm,measles (rubeola) igg antibody,melanoma panel 11 genes,melanoma pancreatic cancer syndrome panel cdk4, cdkn2a,meningitis (viral) profile igg & igm by clia,mercury blood by icpms,metabolic disorder panel,metabolic study for stone,metachondromatosis (metcds),metachromatic leukodystrophy test arsa, aspa, galc, hexa, hexb,metachromatic leukodystrophy (mld),metagenome_db (metagenome genome database),metanephrine free plasma,metanephrine 24 hour urine,metatranscriptome sequencing & analysis,meth haemoglobin,methionine,methotrexate,methyl malonic acid qualitative,urine,methylmalonic acid quantitative serum,methylmalonic acidemia panel mmaa, mmab, mmachc, mm adhc, mut,mgmt methylation test,mic by e strip,micophthalmia, syndromic (mcops) panel,microalbumin,microalbumin/creatinine ratio urine,microarray product of conception,microarray 315k,microarray 315k prenatal with mcc,microarray 750k,microarray 750k prenatal with mcc,microbial identification contig (mid c),microbial identification report (mid r),microbial identification sequence (mid s),microfilaria antibody by card,microfilaria by ps,microfilaria by smear,microfilaria detection by card,microsatellite (per well tube/reaction) (sample 4),microsatellite instability (msi),microvascular complications of diabetes 1 (mvcd1),miller dieker lissencephaly syndrome (mdls),minimal residual disease by flow cytometry,mitochondrial disease panel (37 genes),mll (mixed lineage leukemia gene (mll),mlst 01 (multilocus sequence typing (mlst),mm fish and karyotyping panel,mm fish panel,modified acid fast stain,modified zn stain,mog panel,mog with nmo panel csf,mog with nmo panel seum,mohr tranebjaerg syndrome (mts),monomeric prolactin,monomeric prolactin (active prolactin),mowat wilson syndrome (mows),mp by card method,mpl w 515/s 505 mutation analysis,ms mlpa,mtb pcr,mtb/ntm pcr,mtb mdr (rif/inh),mtb xdr (fluoroquinolones/ injectable drugs),mthfr by pcr,mthfr by sanger,mucopolysaccharides (mps) qualitative urine,mucopolysaccharides (mps) screen,mucopolysaccharides (mps) typing,mucopolysaccharidosis type 3 (mps 3) panel,mucopolysaccharidosis type ii (mps2),mucopolysaccharidosis type ii test ids,mucor racemosus specific igg,multi cancer panel 79 genes,multiminicore disease panel ryr1, sepn1,multiple carboxylase deficiency panel btd, hlcs,multiple endocrine neoplasia, type 1 men1,multiple endocrine neoplasia, type 2 ret,multiple myeloma fish panel(del13q t(4;14) t(11;14) t(14;16) del17p),multiplex pcr (15,17) (11,17)(5,17) for aml,mumps antibody igg,mumps antibody igm,muscular dystrophy, duchennetype (dmd),mustishk stroke panel,mutyh associated polyposis (targeted),mycoplasma pneumonia igg,mycoplasma pneumonia igm,mycoxpert,myelodysplastic syndrome/leukemia panel 21 genes,myofibrillar myopathy panel bag3, cryab, des, dnajb6, fh l1, flnc, ldb3, myot,myoglobin serum,myotonia and paramyotonia congenita panel (2 genes),myotonic dystrophy type 1,myotonic dystrophy type 2,myotubular myopathy, x linked (cnmx),nablus mask like facial syndrome (nmlfs),nail patella syndrome (nps),nance horan syndrome (nhs),nemaline myopathy panel 10 genes,nephronophthisis 1 (nphp1),nephronophthisis panel 12genes,nervous system/brain cancer panel 39 genes,neugen ihc marker,neurodegenration with brain iron accumulation panel (upto 14 genes),neurofibromatosis type 1 test nf1,neurofibromatosis type 2 test nf2,neuronal ceroid lipofuscinoses panel cln3, cln5, cln6, cln8, ctsd, dnajc5, kctd,7mfsd8, ppt1, tpp1,neuropathy, hereditary, with liability to pressure palsies (hnpp),neurotropic virus panel,ngal (netrophil gelatinase associated lipocalin) urine,ngs glycogen storage disease comprehensive panel,ngs mucopolysaccharidoses (mps) comprehensive panel,ngs muscular dystrophy comprehensive panel,ngs myopathy comprehensive panel,ngs dkc1 dyskeratois congenita and shwachman diamond sdbs,ngs 161 gene ocav3 assay ( dna mutations cnvs rna fusions),ngs 409 gene mutation screening (snv indel) + tmb,ngs 546 gene oncomine comprehensive assay plus (dna mutations cnvs rna fusions msi tmb hrr),ngs achromatopsia cone and cone rod dystrophy,ngs adult refsum disease,ngs aicardi goutieres syndrome,ngs albinism,ngs alkaptonuria,ngs alport syndrome,ngs alzheimer dementia and dementia,ngs amyotrophic lateral sclerosis (als),ngs arrhythmia comprehensive panel,ngs arrhythmogenic cardiomyopathy,ngs arthrogryposis,ngs autism panel,ngs bardet biedl,ngs barter syndrome,ngs biotinidase deficiency,ngs b negative scid,ngs bone marrow failure syndrome gene panel,ngs b positive scid,ngs brain iron accumulation syndromes,ngs brain malformations comprehensive panel,ngs brca 1 & 2 with deletions/duplications (germline) (ngs + mlpa),ngs brca1 & 2 (germline)assay,ngs brca1 & 2 (somatic)assay,ngs breast cancer,ngs brugada syndrome,ngs cah deletion & duplication detection,ngs canavan disease,ngs cancer 12 gene panel,ngs cancer hot spot v2 panel (50 gene mutations),ngs cancer comprehensive panel,ngs cardiomyopathy and skeletal muscle disease,ngs cardiomyopathy comprehensive panel,ngs cardiomyopathy,ngs cerebellar ataxia,ngs ceroid lipofuscinosis,ngs charcot marie tooth disease,ngs childhood onset epilepsy,ngs ciliopathies,ngs combined hereditary dementia and amyotrophic lateral sclerosis,ngs combined mito genome plus mito nuclear gene,ngs congenital adrenal hyperplasia,ngs congenital diserythropoetic anaemia,ngs congenital disorders of glycosylation,ngs congenital muscular dystrophy,ngs congenital myasthenic syndrome,ngs congenital myopathy,ngs congenital neutropenia,ngs cornelia de lange syndrome,ngs cortical brain malformations?,ngs cystic fibrosis complete gene sequencing (cftr gene),ngs cystinosis,ngs cystinuria,ngs dba (diamond blackfan anaemia),ngs deafness non syndromic sensorineural autosomal dominant,ngs deafness non syndromic sensorineural autosomal recessive,ngs dilated cardiomyopathy,ngs dmd carrier deletion/duplication testing by mlpa,ngs dna extraction and storage for 5 years,ngs dystonia,ngs early infantile epileptic encephalopathy,ngs epilepsy comprehensive panel,ngs episodic ataxia,ngs eye disorders: comprehensive panel,ngs fabry disease,ngs familial hlh(hemophagocytic lymphohistiocytosis),ngs familial mediterranean fever,ngs fanconi anaemia,ngs fatty acid oxidation defects,ngs female infertility,ngs flecked retina disorders,ngs for hereditary hemolytic anemia (membranopathy and enzymopathy),ngs galactosemia,ngs gene panel test,ngs glucose 6 phosphate dehydrogenase deficiency,ngs glutaric acidemia type i,ngs glycine encephalopathy,ngs gm2 gangliosidosis,ngs hemochromatosis hfe full gene sequencing,ngs hemophilia a and b(factor viii and factor ix),ngs hereditary cancer panel (germline),ngs hereditary cancer panel with brca 1&2 deletions/duplications (ngs + mlpa),ngs hereditary hemochromatosis,ngs hereditary hemorrhagic telangiectasia,ngs hereditary neuropathy sequencing,ngs hereditary parkinson?s disease & parkinsonism,ngs hereditary spastic paraplegia,ngs hereditary thrombophilia,ngs high resolution hla typing,ngs high resolution hla typing (histogenetics),ngs homocystinuria,ngs hrd gene panel,ngs hrr gene panel,ngs hyper ige syndromes,ngs hyperphenylalaninemia,ngs hyperprolinemia,ngs hypertrophic cardiomyopathy,ngs infantile epilepsy,ngs joubert and meckel gruber syndromes,ngs krabbe disease,ngs limb malformation: sequencing,ngs limb girdle muscular dystrophy: sequencing,ngs lissencephaly,ngs liver glycogen storage disease,ngs long qt syndrome,ngs lung cancer 12 gene panel,ngs lysosomal storage disorders comprehensive panel,ngs macular dystrophy/degeneration/stargardt disease,ngs male ifertility,ngs maple syrup urine disease,ngs marfan syndrome,ngs maternal cell contamination,ngs metachromatic leukodystrophy,ngs microphthalmia/anophthalmia/coloboma spectrum,ngs mitochondrial encephalopathy/ leigh syndrome nuclear gene,ngs mitochondrial nuclear gene comprehensive panel,ngs mody panel,ngs mucolipidosis,ngs myoclonic dystonia,ngs nephrotic syndrome gene panel,ngs neuromuscular disorders comprehensive panel,ngs neuropathies comprehensive panel,ngs neurotransmitter disorders,ngs niemann pick disease types a and b,ngs niemann pick type c,ngs non ketotic hyperglycinemia,ngs noonan and rasopathies,ngs obesity panel,ngs omixome duos (ces+mtdna+cnv),ngs omixome solo (ces+mtdna+cnv),ngs omixome trios (ces+mtdna+cnv),ngs oncomine cftna lung assay (dna+rna),ngs oncomine cftna pan cancer assay (dna+rna),ngs oncomine focus assay (52 genes dna mutations cnvs rna fusions),ngs oncomine myeloid v2 gx dna only assay,ngs oncomine myeloid v2 gx rna only assay,ngs oncomine myeloid v2gx assay,ngs oncomine precison gx assay (dna mutations cnvs rna fusions)(liquid biopsy),ngs oncomine precison gx assay (dna mutations cnvs rna fusions),ngs oncomine tumour mutation burden,ngs organic acidemias,ngs overgrowth and macrocephaly syndromes,ngs periodic fever syndromes,ngs polycystic kidney,ngs pompe disease,ngs pontocerebellar hypoplasia,ngs premature ovarian failure: sequencing and fmr1 cgg repeat analysis,ngs prenatal noonan spectrum disorders,ngs prenatal omixome(ces+mtdna+cnv) + mcc,ngs prenatal uniexome(whole exome +mtdna+cnv) + mcc,ngs primary hyperoxiluria,ngs primary immunodeficiency gene panel,ngs progressive external ophthalmoplegia (peo)/optic atrophy nuclear genes,ngs progressive myoclonic epilepsy,ngs propionic acidemia,ngs pulmonary disease: comprehensive panel,ngs pulmonary fibrosis and hermansky pudlak syndrome,ngs pulmonary hypertension,ngs reanalysis and reinterp (panel exome),ngs retina/photoreceptor dystrophy,ngs retinitis pigmentosa,ngs rhizomelic chondrodysplasia punctata spectrum,ngs sandhoff disease,ngs scid comprehensive panel,ngs segregation analysis for 2 mutations in one patient,ngs segregation analysis one mutation for two family members,ngs segregation analysis only per mutation per person,ngs short qt syndrome,ngs single gene (snv+cnv),ngs skeletal dysplasia with increased bone density,ngs sma by mlpa,ngs sma carrier testing by mlpa,ngs sudden cardiac arrest (sca),ngs tay sachs disease,ngs treachers collins syndrome,ngs tuberous sclerosis,ngs typical and atypical hus,ngs tyrosinemia,ngs unicad nipt 5 chromosomes,ngs uniexome duos (whole exome +mtdna+cnv),ngs uniexome solo (whole exome +mtdna+cnv),ngs uniexome trios(whole exome +mtdna+cnv),ngs unifusion seq assay,ngs unipanel(ask us for customized panel) snv+cnv,ngs urea cycle disorders,ngs usher syndrome,ngs waardenburg syndrome,ngs wilson disease,ngs x linked thrombocytopenia,ngs zellweger spectrum disorder,ngs zellweger syndrome,nicotine level / cotinine level (urine),nicotine metabolite, serum,niemann pick type c panel npc1, npc2,nijmegen breakage syndrome test,nk cell (cd16 + cd56),nk cell (cd16 + cd56),nmda antibody csf,nmda antibody serum,nmda receptor antibody (nr1),nmo with mog antibody profile for csf,nocardia culture,non invasive prenatal testing (nipt),noonan syndrome (ns) panel,noonan syndrome panel a2ml1, braf, cbl, kras, map2 k1, map2k2, nras,ptpn11, ra f1, rit1, shoc2, sos1, actb,noonan syndrome with multiple lentigines panel braf, ptpn11, raf1,nor metanephrine free plasma,nor metanephrine 24 hour urine,notch3 mutations,npm1 (nucleophosmin gene (npm1),nras (neuroblastoma ras viral oncogene homolog),ns 1 dengue antigen (rapid),nse neuron specific enolase,nse serum,nt probnp,nystagmus, infantile periodic alternating, x linked (nys1),obesity, severe,occipital horn syndrome (ohs),occult blood stool,oculacutaneous albinism, type ii (oca2),oculo facio cardio dental syndrome test bcor,oligoclonal band csf,oligodontia colorectal cancer syndrome test axin2,opa plus (ngs oncomine precision assay + sbrca),opitz gbbb syndrome, x linked,opportunistic infection panel,oral facial digital syndrome, type 1 test ofd1,organic acidemias panel 31 genes,ornithine transcarbamylase deficiency,orofaciodigital syndrome i (ofd1),osmolality serum,osmolality urine,osmotic fragility test,osteogenesis imperfecta panel col1a1, col1a2, crtap, p3h1,osteogenesis imperfecta, type ii (oi2),osteogenesis imperfecta, type iv,otofaciocervical syndrome 1 (ofc1),oxalate 24 hour urine,p1np,p1np (procollagen type 1 amino terminal propeptide) total,p24 antigen,pallister hall syndrome (phs),pallister killian syndrome (pks),p anca (mpo) by elisa,pap smear staining and reporting,pap smear staining and reporting,pap smear liquid based cytology (lbc),papp a (pregnancy associated plasma protein a),para neoplastic profile(neuronal antigens profile),paracetamol,parietal foramina 1 (pfm),parvovirus b19 igg,parvovirus b19 igm,parvovirus b19, qualitative pcr,pas (periodic acid schif) stain,patau syndrome,paternity test,pcr chlamydia trachomatis & gonorrhoeae combo panel,pcr genital ulcer disease panel,pcr viral eye infection panel,pcr abl kinase mutation for imatinib resistance (irma),pcr adeno virus qualitative,pcr adeno virus quantitative,pcr adrb2 genotyping,pcr alpha thalassemia complete work up,pcr alpha thalassemia deletions/duplication (mlpa),pcr alpha thalassemia sequencing,pcr aml1/eto t(8:21),pcr apc gene mutation family screening,pcr apc gene mutation patient,pcr aspergillus spp. detection,pcr b cell receptor gene rearrangement,pcr bacterial identification (clinical sample),pcr basic colorectal cancer panel a (kras nras brafv600e msi),pcr basic colorectal cancer panel b (kras nras brafv600e),pcr bcr abl minor quantitative (p190),pcr bcr abl(is) quantitative (p210),pcr bcr/abl qualitative major (p210),pcr bcr/abl qualitative minor (p190),pcr bcr abl1 qualitative (p190 p210 & p230),pcr beta thalassemia,pcr beta thalassemia complete work up,pcr bk virus (qualitative),pcr bk virus (quantitative),pcr braf v600e mutation,pcr c kit gene mutation (exon 9 11 13 17) (gist/melanoma),pcr cal r mutation,pcr cbfb/myh11 for inv16,pcr cebpa mutation,pcr chikungunya and dengue (qualitative),pcr chikungunya rna (qualitative),pcr chikungunya rna (quantitative),pcr chimerism follow up sample ( post transplant patient),pcr chimerism (single sample),pcr chlamydia trachomatis,pcr c kit aml (exon 8 17),pcr cmv urine,pcr cmv (qualitative),pcr cmv quantitative,pcr covid 19,pcr cxcr4 mutation testing,pcr cyp2c*19 (clopidogrel),pcr cyp3a5 genotyping,pcr cystic fibrosis,pcr delta beta thalassemia,pcr dengue (qualitative),pcr dengue (quantitative),pcr dengue typing,pcr dnmt3a mutation,pcr dpd gene mutation,pcr duchenne / becker muscular dystrophy (dmd/bmd),pcr e2/pbx1 t(1;19),pcr ebv qualitative,pcr ebv quantitative,pcr egfr (exon 18 19 20 21) mutation,pcr egfr (exon 19) mutation,pcr egfr (exon 21) mutation,pcr endometrial cancer molecular sub classification panel,pcr factor v leiden mutation,pcr fip1l1 pdgfra fusion detection,pcr flt 3 mutation,pcr flt 3 (itd & tkd) mutation,pcr flt3 and npm1 mutation,pcr flt3 itd allelic ratio,pcr freidreichs ataxia mutation analysis,pcr fungal identification (clinical sample),pcr galt mutation,pcr gist panel (kit (exon9 11 13 17)/pdgfra (exon12 18),pcr gonorrhoeae (neisseria gonorrhoeae),pcr hbv dna qualitative,pcr hbv dna quantitative (viral load),pcr hbv dna quantitative (viral load) ivd approved,pcr hbv genotyping,pcr hcv genotyping,pcr hcv quantitative with genotyping,pcr hcv rna (qualitative),pcr hcv rna (quantitative),pcr hemophilia a inversion panel (intron 22 & 1),pcr hemophilia a (intron 1),pcr hemophilia a (intron 22),pcr hepatitis a virus (hav) detection (qualitative),pcr hfe gene mutation (hereditary hemochromatosis ),pcr hhv 6 (human herpesvirus 6) detection qualitative,pcr hhv 7 (human herpesvirus 7) detection qualitative,pcr hiv i proviral dna,pcr hiv i qualitative,pcr hiv i quantitative (viral load),pcr hiv ii quantitative (viral load),pcr hiv 1 drug resistance,pcr hla b,pcr hla b*5701,pcr hla b27,pcr hla b51 (bechets disease),pcr hla celiac disease,pcr hla cw6(c*06 psoriatic arthritis),pcr hpv dna (ffpe block),pcr hpv dna (lbc),pcr hpv screening,pcr hpv typing,pcr h ras mutation,pcr hsv qualitative,pcr hsv quantitative,pcr huntington disease mutation analysis,pcr idh 1/2 mutation,pcr igvh mutation,pcr jak 2 panel [jak2v617f & jak2 exon 12 mutation],pcr jak2 (v617f) mutation,pcr jak2 exon 12 mutation,pcr jak2 reflex panel ( jak v617f negative to exon 12 mutation),pcr japanes encephalitis csf,pcr jc virus qualitative,pcr kit gene mutation (exon 9 11 13 17) (gist/melanoma),pcr k ras mutation,pcr leptospira detection,pcr lpl panel (myd88 + cxcr4),pcr malaria (plasmodium) detection,pcr mgmt methylation assay,pcr microsatelite instability in colon cancer,pcr mll/af4 t(4:11),pcr mpl mutation,pcr mpn reflex panel 1 (bcr abl1 ql jak2v617f jak2 exon 12 calr mpl),pcr mpn reflex panel 2 ( jak2v617f jak2 exon 12 calr mpl),pcr mpn reflex panel 3 ( jak2v617f calr mpl),pcr mpn sure panel(bcrabl ql jak2v617f jak2ex12 mpl calr),pcr mthfr mutation,pcr mucormycosis,pcr myd88 gene mutation,pcr myotonic dystrophy type 1 ( dmpk gene),pcr narcolepsy (hla drb1*15 dqb1*06:02 dqa1*01:02),pcr npm 1 mutation,pcr n ras mutation,pcr nudt15 genotyping,pcr pai 1 genotyping,pcr parvovirus b 19 qualitative,pcr parvovirus b 19 quantitative,pcr pdgfr mutation,pcr pdgfra (exon 12 18) mutation,pcr pik3ca mutation,pcr pml/rara t(15;17) qualitative,pcr pml/rara t(15;17) quantitative,pcr pmp 22 ( peripheral myelin protein 22) by mlpa,pcr pneumocystis pneumonia (pcp),pcr pole gene mutation analysis (sequencing),pcr primary chimerism ( pre transplant patient & donor),pcr prothrombin mutation,pcr respiratory pathogen panel: multiplex rt pcr,pcr ret gene mutation testing (exon 10 11 13 14 15 16),pcr rickettsia detection,pcr rubella detection,pcr salmonella detection,pcr sca detection single form,pcr sma (spinal muscular atrophy) by mlpa,pcr spinal cerebral ataxia ( sca panel 1 2 3 6 7 & 12),pcr std (sexually transmitted diseases) panel,pcr t cell receptor gene rearrangement,pcr t(8;21)aml eto quantitative assay,pcr tb/ntm detection,pcr tel/aml1 t(12:21),pcr tert gene mutation testing,pcr thalassemia complete work up,pcr thiopurine toxicity genotyping (tpmt + nudt15 genotyping),pcr thrombophilia mutation,pcr torch panel,pcr toxoplasma detection,pcr tp53 gene mutation analysis,pcr tpmt genotyping,pcr transplant pathogen mini panel a,pcr transplant pathogen mini panel b,pcr transplant pathogen mini panel c,pcr transplant pathogen mini panel d,pcr transplant pathogen panel (13 pathogens),pcr tropical fever panel,pcr ugtia1 mutation,pcr varicella zoster virus,pcr vesicular rash panel,pcr viral meningitis qualitative,pcr warfarin sensitivity,pcr west nile virus detection,pcr y chromosome microdeletion,pcr zika virus rna (qualitative),pcwh syndrome (pcwh),pdgfra mutations,pdl 1 by immunohistochemistry,pediatric hematologic malignancies panel 16 genes,pediatric nervous system/brain tumors panel 32 genes,pediatric solid tumors panel 47 genes,pelizaeus merzbacher disease (pmd),pelizaeus merzbacher like disease gjc2,penicillium chrysogenum specific igg,periodic fever syndromes panel lpin2, mefv, mvk, nlrp3, pst pip1, tnfrsf1a,peripheral smear study,perlman syndrome test dis3l2,pesticide (qualitative) gastric lavage wadaj,peutz jeghers syndrome stk11,ph for fluid,phadia extended eczema panel,phadia extended rhinitis/asthma panel.,phadia generalized comprehensive panel.,phadia non veg. food panel,phadia veg. food panel,phadia comprehensive food panel (veg. and non veg,phadia generalized comprehensive panel.(veg food),phadiatop adult allergy screening,phadiatop infant allergy screening,phadiatop infant( <5 year) ige,phelan mcdermid syndrome,phenobarbitone,phenol level urine,phenothiazines (qualitative) urine,phenylalanine quantitative plasma,phenytoin (eptoin/epsolin/dilantin),pheochromocytoma marker profile,phosphorus,phosphorus 24 hour urine,pigeon serum protein feather & droppings igg,pitt hopkins syndrome (pths),pituitary hormone deficiency, combined, 4 (cphd4),pivka ii,pivka ii (dcp),pla2 receptor ab by elisa,pla2 receptor antibody quantitative,plasma renin activity,platelet count (fluorescent),platelet gp receptor (gpiib/iiia and gp ib) study by flowcytometry,platinum,pleural fluid analysis,pml/rara,pml rara qualitative by real time pcr,pml rara quantification by real time pcr,pneumo slide panel,pneumocystis carinii detection,pneumoslide panel by ifa igm,pnh by flaer method,pnh by flow (flaer),pompe disease test gaa, lamp2,porphobilinogen urine,porphyria profile (porphobillinogen + ala),posaconazole level,potassium (k+),potassium 24 hour urine,potocki lupski syndrome (ptls),potocki shaffer syndrome (pss),prader?willi syndrome (pws),prader willi/angelman syndrome methylation specific deletion/duplication analysis(ms mlpa),pregnancy test ( upt ),pregnenolone,pre implantation genetic screening (1 embryo) extended,pre implantation genetic screening (1 embryo) stat,prenatal dmd (26 exons); with maternal cell contamination analysis,prenatal fish for 13 18 21 x & y abnormalities,prenatal karyotype & fish,prenatal karyotyping,prenatal karyotyping product of conception(poc),prenatal spinal muscular atrophy; with maternal cell contamination analysis,primary ciliary dyskinesia panel 30 genes,pro calcitonin(pct),product of conception fish,product of conception ngs,progesterone,prolactin,propionic acidemia panel pcca, pccb,prostate cancer panel 12 genes,protein 24 hour urine,protein c,protein c deficiency test proc,protein creatinine ratio,protein electrophoresis,protein s deficiency test pros1,protein s(free),protein with a/g ratio,ps for mp,psa (psa free & psa total),psa total,pt (prothrombin time),pt (prothrombin time) & aptt (activated partial thromboplastin time),pth (parathyroid hormone),pthrp parathyroid hormone releated peptide,pulmonary arterial hypertension panel acvrl1, bmpr2, cav1, eng, kcna5, smad9,pulmonary hypertension, primary, 1(pph1),pus routine examination,pyruvate,pyruvate dehydrogenase e1 alpha deficiency (pdhad),quadruple marker,ra factor,rabies virus antibodies,ras family (kras, hras, nras),rbc folic acid,recombinant chromosome 8 syndrome,recql4 related disorders test,reducing substances stool,renal/urinary tract cancer panel 29 genes,respiratory syncytial virus iga,ret ptc rearrangement,reticulocyte count (automated),retinitis pigmentosa 2 (rp2),retinoblastoma test rb1,retinoschisis 1, x linked, juvenile (rs1),rett and angelman syndromes and related disorders panel (upto 26 genes),rett syndrome mecp2,rett syndrome, congenital variant,reverse t3,rft renal function test (urea, creatinine, sodium, potassium, chloride),rh antibody titre,rhabdoid tumor predisposition syndrome panel smarca4, smarcb1,riboflavin transporter deficiency neuronopathy panel (2 genes),rifampicin by hplc,ripa (ristocetin induced platelet aggregation),rna sequencing & analysis on illumina platforms (sample 35),rna seq_db (rna seq genome database),ros 1,rota virus stool,rota virus stool,rpr (vdrl),rubella (german measles) avidity, igg,rubella igg,rubella igm,rubinstein taybi syndrome 1 (rsts1),s.typhi igm by card,saethre chotzen syndrome (scs),sandhoff disease test hexb, hexa,sanger sequencing (sample 44),sanger sequencing (sample 41),sanger sequencing (sample 45),sanger sequencing of amplicons (single direction),sarcoma panel 40 genes,sbb (sudan black b) stain,sca 12,sca 2,sca 3,sca 6,schwannomatosis test smarcb1, nf2,scl 70 antibody,scleroderma diagnosis panel,scrap material c/s,scrub typhus igg by card,scrub typhus igm by card,scrub typhus igm by elisa,seizures, benign familial neonatal, 1, and/or myokymia,selenium level,semen examination,senior loken syndrome panel cep290, iqcb1, nphp1, nphp4,serotonin serum,serum ascites albumin gradient (saag),severe combined immunodeficiency panel 19 genes,sex growth hormone,sex hormone binding globulin (shbg),sgot,sgpt,short qt syndrome panel cacna1c, cacna2d1,)cacnb2, kcnh2, kcnj2, kcnq1,sickle cell disease (targeted) 3 genetic variants,sickle cell disease (targeted) 3 genetic variants; with maternal cell contamination analysis,sickling test,simpson golabi behmel syndrome test gpc3,simpson golabi behmel syndrome, type 1 (sgbs1),single mutation confirmation by sanger sequencing,sirolimus level,skeletal function test,skin dif(direct immunofluorescence (dif),slide for review (>20 slides + >20 blocks),slide for review (1 slide + 1 block),slide for review (10 15 slides + 10 15 blocks),slide for review (16 20 slides + 16 20 blocks),slide for review (2 slides + 2 blocks),slide for review (3 slides + 3 blocks),slide for review (4 to 6 slides + 4 to 6 blocks),slide for review (5 slides + 5 blocks),slide for review (6 slides + 6 blocks),slide for review (7 to 9 slides + 7 to 9 blocks),slit skin smear examination with modifiled acid fast stain,sm ab,small cell carcinoma of the ovary (hypercalcemic type) test smarca4,small fiber neuropathy scn9a, scn10a,smith lemli opitz syndrome (slos),smith magenis syndrome (sms),snp det08 (snp detection in 500 bases),sodium (na+),sodium 24 hour urine,sodium urine,soluble transferrin receptor stfr,somatic mutation panel 56 genes,sotos syndrome 1 (sotos1),sotos syndrome test nsd1,speech language disorder 1 (spch1),sperm dna fragmentation,spermatogenic failure, y linked (spgfy) panel,spinal muscular atrophy by mlpa,spinal muscular atrophy panel (2 genes),split hand/foot malformation (shfm) panel,sputum for afb,sputum for cytology,sputum for eosinophil,sputum routine & micro,ss a by elisa,ss a/ro (60 kda 52 kda),ss a/ro (60 kda),ss b by elisa,ss b/la,stem cell count(cd 34 count),sterility test for biological indicator,sterility test for blood product,sterility test for water,steroid detection in unknown drug powder,stickler syndrome (stl) panel,stone analysis,stone analysis by automated machine,stool antigen h.pylori,stool examination,stool examination for parasite,stool for hanging drop,stool for vibrio cholera,stool occult blood,streprococcus pneumoniae (pneumococcal) ag urine,streptococcus pneumoniae antigen,stress cytogenetic (fanconi anemia),strongyloidiasis serology serum by eia,str plate12 (microsatellite genotyping),str rrp10 (microsatellite genotyping(ready to run)),succinylacetone,succinylacetone, blood,sucrose lysis test,sudan iii stain for fat in stool,sudan iv stain stool,swine flu by pcr,syndromic neurodevelopmental epilepsy panel 16 genes,synovial fluid gram z n stain,synovial fluid routine examination,synovial fluid uric acid,synpolydactyly 1(spd1),syphilis (total) antibodies,syphilis antibody,systemic scierosis profile,t3,t4,tacrolimus level,tamoxifen sensitivity test (cyp2d6 mutations),tay sachs disease mutation analysis hexa,tb gold,tb pcr by gene expert,tb pcr from block,tb pcr from tissue,tb pcr blood,tb pcr csf,tb pcr fluid,tb pcr urine,tel/aml1,testosterone,tetanus toxoid igg antibodies,tft thyroid function test basic (t3, t4, tsh),tft thyroid function test advance (free t3, free t4, tsh),thallium by icpms,theophylline,thiopurine metabolite,thrombin time,thrombocytopenia, paris trousseau type (tcpt),thrombocytopenia absent radius syndrome (tar),thrombophilia panel,thrombophilia panel (mthfr, factor v and factor ii) by pcr,thyroglobulin,thyroid cancer panel 11 genes,thyroid stimulating immunoglobulin (tsi),thyroxine binding globulin (tbg) level serum,timothy syndrome cacna1c (exon 1 is not included in deletion/ duplication analysis),tissue processing block cutting and staining for 1st block & slide,2nd block cutting and slide staining for same patient,extra slide staining (h & e),grossing charges per sample,tissue transglutaminase ttg dgp screen,t lymphocyte subset analysis,tms newborn screening for metabolic disorder,tms extended (new born screening) up to six month,tnf alpha,toe syndactyly, telecanthus, and anogenital and renal malformation,tooth agenesis, selective 3 (sthag3),torch 5 parameters igg,torch 5 parameters igm,torch complex 10 parameter (elisa ),torch complex 8 parameter (elisa),torch panel avidity igg,total bilirubin,total iron binding capacity (tibc),total protein fluid,total protein serum,townes brocks syndrome (tbs),townes brocks syndrome test sall1,toxo igg,toxo igm,toxoplasma avidity, igg, serum,toxoplasma dna detection, pcr,tpha,tpha,csf,tpmt enzyme activity,tpmt genotyping,transferrin level,transferrin saturation,transplant donor derived cell free dna ; % dd cfdna,transplant hla typing (a b c drb1 drb3 4 5 dqab),transplant hla typing (a b drb1),transplant hla typing for patient and donor,transplant hla typing individual locus (a/b/c/dr/dq),transplant lymphocyte cross match report (cdc),transplant panel reactive antibody report (pra) class i & ii report,transplant single antigen screen test (sa qualitative class i ii & mic a),transplant single antigen quantitative test report (single antigen class i & ii ),transplant t & b cell flow cross match (fcxm) report,transthyretin amyloidosis ttr,treacher collins syndrome 1 (tcs1),trichorhinophalangeal syndrome (trps) panel,tricyclic antidepressants (tca),triglyceride,triglyceride fluid,triglyceride urine,triple marker,triple x syndrome,trisomy 12,trisomy 8,troponin t,troponin i (high sensitive) by cmia,troponin i (high sensitive) by clia,tryptase,tsh,tsh receptor antibody,ttg iga,ttg igg,ttg dgp screen test,tuberculosis culture,tuberous sclerosis (tsc) panel,tuberous sclerosis complex panel tsc1, tsc2,turner syndrome,type vi collagenopathy panel col6a1, col6a2, col6a3,typhi dot by card,typhi dot igg,typhi dot igm,u1rnp (rnp) ab,u1 snrnp,uibc,ulnar mammary syndrome (ums),unifungal pcr,uniseq 01 (purified plasmid/pcr product sequencing service),uniseq 02 (r e.coli clone sequencing service),unstable hb,upt (urine pregnancy test),urea,urea clot lysis test,urea cycle disorders panel aldh18a1, arg1, asl, ass1, cp s1, hmgcl, oatotc, slc25a13, slc25a15,urea fluid,urea nitrogen 24 hour urine,uric acid 24 hour urine,uric acid serum,uric acid urine,urine afb,urine albumin,urine amino acid quantitative by lcms,urine calcium,urine calcium creatine ratio,urine chloride,urine copper (spot),urine cotinine (nicotine) level by card,urine cotinine by hplc,urine creatinine (random),urine drug screen amphetamine,urine drug screen barbiturate,urine drug screen benzodiazepine,urine drug screen cocaine/benzoylecgonine,urine drug screen marijuana,urine drug screen methadone,urine drug screen methamphetamine,urine drug screen opiates/morphine,urine drug screen phencyclidine,urine drug screen tetra hydro cannabinol,urine drug screen (6 drugs),urine drug screen (9 drugs),urine electrolytes (random),urine for chyluria,urine for cytology,urine for eosinophil,urine for fat globules,urine for haemoglobinuria,urine for heavy metals,urine for phase contrast microscopy,urine for protein electrophoresis,urine for reducing substances,urine for specific gravity,urine free light chain assay,urine glucose,urine hemosiderin,urine immunofixation,urine kappa light chain,urine magnesium,urine myoglobin,urine organic acid,urine ph,urine phosphorus(random),urine porphobilinogen qualitative,urine porphobillinogen quantitative (24 hour),urine porphobillinogen quantitative (spot),urine potassium,urine protein,urine protein creatinine ratio,urine protein electrophoresis,urine rbc morphology by phase contrasmicroscopy,urine routine examination,urine uric acid,urine uric acid creatinine ratio,urine urobilinogen,valproic acid level (sodium valporate),van der woude syndrome 1 (vws1),van der woude syndrome panel grhl3, irf6,vancomycin,varicella zoster igg,varicella zoster igm,vdrl,vdrl csf,velocardiofacial syndrome (vcfs),vgkc antibody serum,vgkc antibody, csf,vitamin a,vitamin b1,vitamin b12,vitamin b2,vitamin b6 (pyridoxine),vitamin c,vitamin d,vitamin d gold (covers vitamin d2 vitamin d3 & d),vitamin e,vitamin k,vitamin k1,vitek cs blood aerobic with vitek automation,vitek cs csf with vitek automation,vitek identification,vitek identification and sensitivity,vitek sensitivity,vizag one marker,vizag pdl1(b7h1p),vma 24 hour urine,von hippel lindau syndrome vhl by pcr,von willebrand disease (vwd) test,von willebrand factor (vwf) study,von willibrand antigen,voriconazole level,waardenburg syndrome (ws) panel,warfarin sensitivity (cyp2c9, vkorc1),was related disorders test,weak z n stain,weaver syndrome test ezh2,weil felix test,werner syndrome test wrn,wet mount preparation,whole exome sequencing,widal,william syndrome (7q11.23),williams beuren region duplication syndrome,wilms tumor panel dkn1c, dis3l2, gpc3, wt1,wilms tumor, aniridia, genitourinary anomalies and,wilson disease test atp7b,witkop syndrome,wolf hirschhorn syndrome,womens hereditary cancers (hereditary breast and gynecologic cancers) 22 genes,wt1 related disorders test,x, y fish panel,xdr tb rapid genotyping,xdr tb rapid genotyping test 2nd line (aminoglycosides/fluoroquinol ones/capreomycin),xdr tb rapid genotyping test 2nd line (aminoglycosides/fluoroquinolones/capreomycin) lpa,x inactivation, familial skewed,x linked adrenoleukodystrophy (x ald),xpert hcv viral load,xpert hiv viral load,xpert hiv 1 quantitative viral load with cd4 count,xpert xdr tb,y chromosome microdeletion,yersinia culture stool,yersinia enterocolitica antigen stool,zika virus qualitative pcr,zinc level,znt8 (zinc transporter 8) antibody clia...