Genetic Tests
Comprehensive guides to genetic tests from WES and WGS to NIPT and pharmacogenomics.
Genetic Tests
Whole Exome Sequencing (WES) at Gene Negar Ayandegan
Whole Exome Sequencing (WES) for rare and inherited diseases and unexplained genetic conditions, offered by Gene Negar Ayandegan in Tehran.
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Whole Genome Sequencing (WGS) at Gene Negar Ayandegan
Whole Genome Sequencing (WGS) for comprehensive analysis of human DNA, including coding and non-coding regions.
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NGS Cancer Panel at Gene Negar Ayandegan
Targeted NGS panels analyzing somatic variants to guide targeted therapy in solid tumors and hematologic malignancies.
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Hereditary Cancer Panel at Gene Negar Ayandegan
Hereditary cancer gene panel to assess inherited risk of familial cancers and cancer predisposition syndromes.
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BRCA1 and BRCA2 Testing at Gene Negar Ayandegan
BRCA1 and BRCA2 gene testing to assess inherited risk of breast, ovarian, prostate and pancreatic cancer.
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Sanger Sequencing at Gene Negar Ayandegan
Sanger sequencing for variant confirmation, single-gene analysis and plasmid sequencing.
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Fragment Analysis at Gene Negar Ayandegan
Fragment analysis for STR, microsatellite, short alleles and DNA fragment sizing.
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MLPA Testing at Gene Negar Ayandegan
MLPA testing for detecting exon-level deletions and duplications in genetic diseases.
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QF-PCR Testing at Gene Negar Ayandegan
QF-PCR for rapid detection of common chromosomal aneuploidies in prenatal samples and recurrent pregnancy loss.
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Non-Invasive Prenatal Testing (NIPT) at Gene Negar Ayandegan
NIPT screening for common fetal chromosomal aneuploidies using maternal blood.
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Prenatal Genetic Testing at Gene Negar Ayandegan
Comprehensive prenatal genetic testing including NIPT, QF-PCR, CVS, amniocentesis and fetal genomic analysis.
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Carrier Screening at Gene Negar Ayandegan
Carrier screening to identify parents who may transmit recessive genetic conditions to offspring.
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PGT-A at Gene Negar Ayandegan
PGT-A screens IVF embryos for aneuploidy before transfer.
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PGT-M at Gene Negar Ayandegan
PGT-M to prevent transmission of monogenic diseases to offspring.
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Pharmacogenomics at Gene Negar Ayandegan
Pharmacogenomic testing to guide drug and dose selection based on the patient's genotype.
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STR / HID Testing at Gene Negar Ayandegan
Human identification via STR analysis for paternity, kinship and forensic applications.
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Y Chromosome Microdeletion Test at Gene Negar Ayandegan
Analysis of AZF microdeletions of the Y chromosome in male infertility.
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Mitochondrial DNA Testing at Gene Negar Ayandegan
Mitochondrial DNA analysis for diagnosing maternally inherited metabolic and neurologic diseases.
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