Genetic tests :: Dobrolab

Prenatal genetic tests

Postnatal genetic tests

Title	Price (uah)
"FISH study, 5 chromosomes (material - ejaculate)"	4200
GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per element)	21700
GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per pair)	41230
Detection of HLA-B27 Antigen	1660
Karyotyping (material - blood)	3710
Karyotyping (material - blood) (cito)	5410
Lactase intolerance, PCR	1140
Polymorphism of trombophilia genes (prothrombin, Leiden mutation, MTHFR)	3340
Gilbert's syndrome, familial non-hemolytic-non-obstructive jaundice / toxicity RI	2500
Folate cycle, gene polymorphism (MTHFR C677T and MTHFR A1298C)	1750
Zygosity determination of the RHD gene	4140
GEN_Diagnosis of Noonan syndrome (exon sequencing of the PTPN11 gene)	12100
GEN_Molecular karyotyping (chromosomal microarray analysis, CGH) postnatally for children and adults, Illumina 300K	28410
GEN_DNA diagnosis of Y chromosome microdeletions	2710
GEN_Large genetic panel (NGS, as described on the blueprintgenetics website)	36260
GEN_Leber congenital amaurosis genetic panel (NGS, 28 genes, medium, OP1701)	32120
GEN_Corneal Dystrophy Gene Panel (NGS, 29 genes, medium, OP1601)	32120
GEN_Retinal Dystrophy Gene Panel (NGS, 351 genes, large, OP0801)	36260
GEN_Macular Dystrophy Gene Panel (NGS, 28 genes, medium, OP0101)	32120
GEN_Retinitis Pigmentosa Gene Panel (NGS, 159 genes, large, OP0901)	36260
GEN_Premature Ovarian Depletion Gene Panel (NGS, 16 genes, small, EN0901)	33820
GEN_Autism Spectrum Disorders Genetic Panel (NGS, 75 genes, medium, NE0101)	32120
GEN_Usher syndrome genetic panel (NGS, 21 genes, small, OP1101)	28410
GEN_Complete Epilepsy Genetic Panel (NGS, 511 genes, large, NE1001)	36260
GEN_Complete genetic cardiology screening (NGS, 260 genes, large, CA1301)	36260
GEN_Complete genetic proactive screening (cardio+oncology) (NGS, 181 genes, large, PS0005)	36260
GEN_Narrow genetic panel (NGS, as described on the blueprintgenetics website)	28410
GEN_Neuro-ophthalmic genetic panel (NGS, 97 genes, medium, OP1301)	32120
GEN_Whole Exome Sequencing (WES, Blueprint, WE0501)	41770
GEN_Single Gene Sequencing (Blueprintgenetics)	24380
GEN_Mid-Range Genetic Panel (NGS, as described on the Blueprintgenetics website)	32120
Examination of ejaculate using FISH and TUNEL	6580
Chromosomal passport (expert examination)	5730

TitlePrice (uah)

"FISH study, 5 chromosomes (material - ejaculate)"

4200 uah

GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per element)

21700 uah

GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per pair)

41230 uah

Detection of HLA-B27 Antigen

1660 uah

Karyotyping (material - blood)

3710 uah

Karyotyping (material - blood) (cito)

5410 uah

Lactase intolerance, PCR

1140 uah

Polymorphism of trombophilia genes (prothrombin, Leiden mutation, MTHFR)

3340 uah

Gilbert's syndrome, familial non-hemolytic-non-obstructive jaundice / toxicity RI

2500 uah

Folate cycle, gene polymorphism (MTHFR C677T and MTHFR A1298C)

1750 uah

Zygosity determination of the RHD gene

4140 uah

GEN_Diagnosis of Noonan syndrome (exon sequencing of the PTPN11 gene)

12100 uah

GEN_Molecular karyotyping (chromosomal microarray analysis, CGH) postnatally for children and adults, Illumina 300K

28410 uah

GEN_DNA diagnosis of Y chromosome microdeletions

2710 uah

GEN_Large genetic panel (NGS, as described on the blueprintgenetics website)

36260 uah

GEN_Leber congenital amaurosis genetic panel (NGS, 28 genes, medium, OP1701)

32120 uah

GEN_Corneal Dystrophy Gene Panel (NGS, 29 genes, medium, OP1601)

32120 uah

GEN_Retinal Dystrophy Gene Panel (NGS, 351 genes, large, OP0801)

36260 uah

GEN_Macular Dystrophy Gene Panel (NGS, 28 genes, medium, OP0101)

32120 uah

GEN_Retinitis Pigmentosa Gene Panel (NGS, 159 genes, large, OP0901)

36260 uah

GEN_Premature Ovarian Depletion Gene Panel (NGS, 16 genes, small, EN0901)

33820 uah

GEN_Autism Spectrum Disorders Genetic Panel (NGS, 75 genes, medium, NE0101)

32120 uah

GEN_Usher syndrome genetic panel (NGS, 21 genes, small, OP1101)

28410 uah

GEN_Complete Epilepsy Genetic Panel (NGS, 511 genes, large, NE1001)

36260 uah

GEN_Complete genetic cardiology screening (NGS, 260 genes, large, CA1301)

36260 uah

GEN_Complete genetic proactive screening (cardio+oncology) (NGS, 181 genes, large, PS0005)

36260 uah

GEN_Narrow genetic panel (NGS, as described on the blueprintgenetics website)

28410 uah

GEN_Neuro-ophthalmic genetic panel (NGS, 97 genes, medium, OP1301)

32120 uah

GEN_Whole Exome Sequencing (WES, Blueprint, WE0501)

41770 uah

GEN_Single Gene Sequencing (Blueprintgenetics)

24380 uah

GEN_Mid-Range Genetic Panel (NGS, as described on the Blueprintgenetics website)

32120 uah

Examination of ejaculate using FISH and TUNEL

6580 uah

Chromosomal passport (expert examination)

5730 uah

Oncology hereditary panels

Microbiome

Pre-implantation diagnostics

General clinical studies

Immunohematological tests

Biochemical tests

Complex tests

Hormone tests

Pregnancy and prenatal screening

Immunological and autoimmune tests

Infections

Microbiological studies

Cytological tests

Genetic tests

Pathomorphological studies and study of tumors

Useful information

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