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GEN_Whole Exome Sequencing (WES, Blueprint, WE0501)

GEN_Whole Exome Sequencing (WES, Blueprint, WE0501)

Genetic tests Postnatal genetic tests

Price (uah): 39400 uah

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General clinical studies

General clinical studies

Immunohematological tests

Immunohematological tests

Biochemical tests

Biochemical tests

Complex tests

Complex tests

Hormone tests

Hormone tests

Pregnancy and prenatal screening

Pregnancy and prenatal screening

Immunological and autoimmune tests

Immunological and autoimmune tests

Infections

Infections

Microbiological studies

Microbiological studies

Cytological tests

Cytological tests

Genetic tests

Genetic tests

Pathomorphological studies and study of tumors

Pathomorphological studies and study of tumors

Similar research

Title	Price (uah)
Lactase intolerance, PCR	1070
Detection of HLA-B27 Antigen	1260
Polymorphism of trombophilia genes (prothrombin, Leiden mutation, MTHFR)	2950
"FISH study, 5 chromosomes (material - ejaculate)"	4200
GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per element)	18500
GEN_CarrierSeq - screening for carriers of genetic mutations, monogenic and hereditary diseases (genetic diagnosis, NGS, per pair)	34300
Gilbert's syndrome, familial non-hemolytic-non-obstructive jaundice / toxicity RI	2100
Zygosity determination of the RHD gene	3900
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	26800

TitlePrice (uah)

Lactase intolerance, PCR

1070 uah

cart

Detection of HLA-B27 Antigen

1260 uah

cart

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

2950 uah

cart

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

4200 uah

cart

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

18500 uah

cart

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

34300 uah

cart

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

2100 uah

cart

Zygosity determination of the RHD gene

3900 uah

cart

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

12100 uah

cart

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

26800 uah

cart