Exome, genome & chromosome tests in Mumbai

Clinical Exome Sequencing (CES)

A focused version of exome sequencing, analysing the ~5,000 genes with well-established links to known genetic diseases — faster and more affordable than the full exome.

Karyotyping (Blood)

Examines the number and structure of your chromosomes under a microscope — used to diagnose chromosomal conditions like Down syndrome, or investigate infertility and recurrent miscarriage.

Whole Exome Sequencing (WES)

Reads the protein-coding portion of your entire genome (~20,000 genes) — the broadest single test for diagnosing an unexplained genetic condition.

Whole Genome Sequencing (WGS)

Reads essentially all of your DNA, coding and non-coding — the most complete genetic test available, used when exome sequencing hasn't found an answer.

Autopsy Panel (With CES)

Autopsy Panel (With CES) analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

C Banding

C Banding is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to find extra, missing or…

C Banding and NOR Staining

C Banding and NOR Staining is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to find…

Clinical Exome + Mitochondrial Genome

Clinical Exome + Mitochondrial Genome analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Clinical Exome Sequencing (Expedited TAT)-PND

Clinical Exome Sequencing (Expedited TAT)-PND analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Clinical Exome Sequencing-Duo

Clinical Exome Sequencing-Duo analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Clinical Exome Sequencing-ET

Clinical Exome Sequencing-ET analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Clinical Exome Sequencing-Trio

Clinical Exome Sequencing-Trio analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Constitutional karyotyping (CK)

Constitutional karyotyping (CK) is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to…

Epitome-Blood Karyotype

Epitome-Blood Karyotype is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to find…

FISH for Angelman syndrome

FISH for Angelman syndrome is a FISH test that uses fluorescent probes to look for a specific small chromosome deletion linked to a known syndrome (such as 22q11.2 deletion, Prader-Willi, Angelman…

FISH for Prader-Willi Syndrome

FISH for Prader-Willi Syndrome is a FISH test that uses fluorescent probes to look for a specific small chromosome deletion linked to a known syndrome (such as 22q11.2 deletion, Prader-Willi…

FISH for William's Syndrome

FISH for William's Syndrome is a FISH test that uses fluorescent probes to look for a specific small chromosome deletion linked to a known syndrome (such as 22q11.2 deletion, Prader-Willi…

FISH-22q Microdeletion

FISH-22q Microdeletion is a FISH test that uses fluorescent probes to look for a specific small chromosome deletion linked to a known syndrome (such as 22q11.2 deletion, Prader-Willi, Angelman or…

Fragile X + Clinical Exome Sequencing (Only For Males)

Fragile X + Clinical Exome Sequencing (Only For Males) analyses the roughly 5,000 genes with established links to inherited disease — a focused alternative to whole exome sequencing.

Fragile X + Whole Exome Sequencing

Fragile X + Whole Exome Sequencing reads the protein-coding regions (the exome) of about 20,000 genes at once, where most known disease-causing variants are found.

NOR Staining

NOR Staining is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to find extra, missing…

Prenatal Karyotype+22q Microdeletion

Prenatal Karyotype+22q Microdeletion examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal conditions such as Down syndrome.

Prenatal Karyotype+FISH 13,18,21 Chromosomes

Prenatal Karyotype+FISH 13,18,21 Chromosomes examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal conditions such as Down…

Prenatal Karyotype+FISH Chromosome 13,21

Prenatal Karyotype+FISH Chromosome 13,21 examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal conditions such as Down syndrome.

Prenatal Karyotype+FISH Chromosome 21

Prenatal Karyotype+FISH Chromosome 21 examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal conditions such as Down syndrome.

Prenatal Karyotype+FISH Chromosomes 13,18,21,XY+ 22q Microdeletion

Prenatal Karyotype+FISH Chromosomes 13,18,21,XY+ 22q Microdeletion examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal…

QF PCR+Prenatal Karyotype

QF PCR+Prenatal Karyotype examines the baby's chromosomes from amniotic fluid or CVS under the microscope to give a definite diagnosis of chromosomal conditions such as Down syndrome.

Spectral Karyotyping

Spectral Karyotyping is a chromosome analysis (karyotype). Cells from a blood sample are grown, and the number and structure of all 46 chromosomes are examined under the microscope to find extra…

Whole Exome + Mitochondrial Genome

Whole Exome + Mitochondrial Genome reads the protein-coding regions (the exome) of about 20,000 genes at once, where most known disease-causing variants are found.

Whole Exome Sequencing -Expedited TAT

Whole Exome Sequencing -Expedited TAT reads the protein-coding regions (the exome) of about 20,000 genes at once, where most known disease-causing variants are found.

Whole Exome Sequencing (Trio)

Whole Exome Sequencing (Trio) reads the protein-coding regions (the exome) of about 20,000 genes at once, where most known disease-causing variants are found.

Whole Exome Sequencing-Duo

Whole Exome Sequencing-Duo reads the protein-coding regions (the exome) of about 20,000 genes at once, where most known disease-causing variants are found.