PGD-SEQ* kits offer over 300 gene panels to research embryo status of common and rare monogenic/single-gene diseases for IVF
With the power of Ion Torrent NGS technology, a single sample can be used for both PGT-A and PGT-M IVF investigations within a simplified and integrated workflow.
Each PGD-SEQ kit contains library preparation reagents necessary to enable preimplantation genetic testing for monogenetic/single-gene disorders (PGT-M). Benefits of using targeted NGS for PGT-M include:
- Verified for use with the Ion GeneStudio S5 System or Ion PGM System
- Complete kit reagents and targeted PGT-M library to analyze 15 samples
- Comprehensive familial carrier status using proprietary linkage analysis software
- Compatible with the Ion ReproSeq PGS Kit for combined PGT-M and PGT-A analysis from a single research sample
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| Gene | Disease research area | PGD-SEQ Panel Cat. No. |
|---|---|---|
| SMN1 | Spinal muscular atrophy | BA03784 |
| POMK | Muscular dystrophy-dystroglycanopathy | BA03785 |
| ACADM | Medium chain acyl-CoA dehydrogenase deficiency | BA03798 |
| BBS10 | Bardet-Biedl syndrome 10 | BA03799 |
| CFTR | Cystic fibrosis | BA03800 |
| MPZ (CMT1B) | Charcot-Marie-Tooth type 1B | BA03801 |
| COL11A1 | Stickler syndrome | BA03802 |
| COL1A1 | Osteogenesis imperfecta (COL1A1) | BA03803 |
| COL2A1 | Spondyloepiphyseal dysplasia | BA03804 |
| CYP21A2 | Congenital adrenal hyperplasia | BA03805 |
| D4Z4 | Facioscapulohumeral muscular dystrophy (FSHD) | BA03806 |
| DMD | Duchenne muscular dystrophy | BA03807 |
| DMPK | Steinert disease (Myotonic dystrophy type 1) | BA03808 |
| DYNC2H1 | Jeune syndrome | BA03809 |
| EVC, EVC2 | Ellis-van Creveld syndrome | BA03811 |
| EXT1 | Exostoses type 1 | BA03812 |
| EXT2 | Exostoses type 2 | BA03813 |
| F8 | Hemophilia A | BA03814 |
| FBN1 | Marfan syndrome | BA03815 |
| FUS | Amyotrophic lateral sclerosis (ALS) | BA03817 |
| GALNS | Mucopolysaccharidosis IV | BA03818 |
| GJA1 | Oculodentodigital dysplasia | BA03819 |
| HBB | Beta thalassemia | BA03820 |
| HTT | Huntington | BA03821 |
| HEXA | Tay-Sachs disease | BA03822 |
| HLA | Histocompatibility | BA03823 |
| IL2RG | X-linked combined immunodeficiency | BA03824 |
| ABCD1 | Adrenoleukodystrophy X-Linked | BA03825 |
| LAMB3 | Junctional epidermolysis bullosa | BA03826 |
| LMNA | Dilated cardiomyopathy | BA03827 |
| MSH2 | Lynch syndrome | BA03828 |
| MEN1 | Multiple endocrine neoplasia | BA03829 |
| NOTCH3 | CADASIL | BA03830 |
| OTC | Ornithine transcarbamylase deficiency | BA03831 |
| PKD1 | Polycystic kidney disease 1 | BA03832 |
| PKD2 | Polycystic kidney disease 2 | BA03833 |
| PKHD1 | Polycystic kidney disease AR | BA03834 |
| RET | Multiple endocrine neoplasia type 2 | BA03835 |
| RHO | Retinitis pigmentosa | BA03836 |
| RYR1 | Central core disease | BA03837 |
| ATL1 | Spastic paraplegia type 3A | BA03838 |
| TBX5 | Holt-Oram syndrome | BA03839 |
| TCOF1 | Treacher-Collins syndrome | BA03840 |
| TSC1 | Tuberous sclerosis | BA03841 |
| TWIST1 | Saethre-Chotzen syndrome | BA03842 |
| UNC13D | Hemophagocytic lymphohistiocytosis 3 | BA03843 |
| HBA1, HBA2 | Alpha thalassemia | BA03864 |
| Custom panel | BA04160 | |
| ANTXR2 | Hereditary systemic hyalinosis | BA04277 |
| ABCB11 | Progressive familial intrahepatic cholestasis | BA04362 |
| L1CAM | Hydrocephalus | BA04382 |
| ALS2 | Amyotrophic lateral sclerosis (ALS) | BA04383 |
| BBS4 | Bardet-Biedl syndrome 4 | BA04384 |
| ATXN2 | Spinocerebellar ataxia type 2 | BA04385 |
| CENPJ | Microcephaly | BA04386 |
| PMM2 | Congenital disorder of glycosylation | BA04387 |
| CHM | Choroideremia | BA04388 |
| CSF1R | Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP ) | BA04389 |
| EDA | Hypohidrotic ectodermal dysplasia | BA04390 |
| FGFR3 | Achondroplasia | BA04391 |
| HNF1B | Renal cysts and diabetes syndrome | BA04392 |
| MYBPC3 | Hypertrophic cardiomyopathy | BA04393 |
| MYH7 | Miopathy | BA04394 |
| PAX6 | Aniridia | BA04395 |
| PMP22 (CMT1A) | Charcot-Marie-Tooth type 1A and 1E | BA04396 |
| SPAST | Spastic paraplegia type 4 | BA04397 |
| TGFBR1 | Loeys-Dietz syndrome | BA04398 |
| TP53 | Li-Fraumeni syndrome | BA04399 |
| VHL | Von Hippel-Lindau syndrome | BA04400 |
| VPS13B | Cohen syndrome | BA04401 |
| ATXN1 | Spinocerebellar ataxia type 1 | BA04402 |
| MKS1 | Meckel Gruber syndrome | BA04403 |
| PLP1 | Pelizaeus-Merzbacher disease | BA04404 |
| TNXB | Ehlers-Danlos syndrome, classical-like | BA04405 |
| AIMP2 | Progressive neurodevelopmental disorder | BA04406 |
| GALC | Krabbe disease | BA04549 |
| CLCN1 | Myotonia congenita | BA04569 |
| TNNT2 | Dilated cardiomyopathy | BA04570 |
| PHEX | Hypophosphatemic rickets | BA04571 |
| ACADVL | Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency | BA04572 |
| AR | Kennedy disease | BA04573 |
| GALT | Galactosemia | BA04574 |
| BSCL2 | Spastic paraplegia | BA04575 |
| BRCA1 | Breast-ovarian cancer syndrome | BA04576 |
| NF1 | Neurofibromatosis type 1 | BA04577 |
| CEP290 | Meckel-Gruber syndrome | BA04578 |
| PEX16 | Zellweger syndrome | BA04579 |
| AGL | Glycogen storage disease type III | BA04582 |
| LAMA3 | Epidermolysis bullosa | BA04584 |
| RB1 | Retinoblastoma | BA04586 |
| SCN4A | Paramyotonia | BA04587 |
| LAMA2 | LAMA2-related muscular dystrophy | BA04588 |
| BRCA2 | Breast-ovarian cancer syndrome 2 | BA04603 |
| COL7A1 | Dystrophic epidermolysis bullosa | BA04604 |
| ECHS1 | Mitochondrial syndrome | BA04605 |
| FH | Hereditary leiomyomatosis and renal cell cancer (HLRCC) | BA04606 |
| PRPH2 | Stargardt disease | BA04607 |
| COQ4 | Primary coenzyme Q10 deficiency | BA04622 |
| TGM1 | Hereditary ichthyosis (9/18/2020 Luis A approved the change to Lamellar ichthyosis) | BA04631 |
| CPLANE1 (C5orf42) | Joubert syndrome | BA04632 |
| ADAT3 | Mental retardation | BA04633 |
| ITGA2B | Glanzmann thrombasthenia | BA04634 |
| TRIP11 | Achondrogenesis type 1A | BA04652 |
| GRIA3 | Mental retardation | BA04653 |
| GLB1 | GM1 ganglioside | BA04654 |
| C12orf57 | Temtamy syndrome | BA04655 |
| POMGNT2 | Walker-Warburg syndrome | BA04656 |
| GLDC | Glycine encephalopathy | BA04657 |
| COL6A1 | Ullrich myopathy | BA04658 |
| ELAC2 | Hypertrophic cardiomyopathy | BA04659 |
| SMPD1 | Niemann-Pick disease (SMPD1) | BA04660 |
| IDS | Mucopolysaccharidosis type II (MPS II - Hunter syndrome) | BA04681 |
| HMGCL | HMGCL deficiency | BA04725 |
| LIPH | Autosomal recessive hypotrichosis | BA04726 |
| PHKB | Glycogen storage disease type IX | BA04727 |
| RAB3GAP1 | RAB18 deficiency | BA04728 |
| OSTM1 | Osteopetrosis, AR 5 | BA04730 |
| SLC5A7 | Myasthenic syndrome, congenital, 20, presynaptic | BA04731 |
| ECM1 | Lipoid proteinosis | BA04732 |
| TUSC3 | Mental retardation, autosomal recessive 7 | BA04733 |
| RPGRIP1 | Leber congenital amaurosis | BA04734 |
| PDE6C | Achromatopsia / Cone-rod dystrophy | BA04735 |
| DNAH5 | Primary ciliary dyskinesia/Heterotaxy | BA04736 |
| WDR62 | Autosomal recessive primary microcephaly (WDR62) | BA04762 |
| SLC26A3 | Congenital secretory diarrhea, chloride type | BA04763 |
| ABCB4 | Intrahepatic cholestasis type 3 | BA04764 |
| ALPL | Hypophosphatasia | BA04804 |
| HBB, HLA | Beta-thalassemia & Histocompatibility | BA04819 |
| APC | Familial adenomatous polyposis (FAP) | BA04820 |
| CCM2 | Cerebral cavernous malformations | BA04821 |
| OTOF | DFNB9 Nonsyndromic Hearing Loss | BA04822 |
| WAS | Wiskott-Aldrich syndrome | BA04823 |
| COL4A5 | Alport syndrome | BA04824 |
| KCNH2 | Short QT syndrome | BA04825 |
| TCTN2 | Joubert syndrome | BA04826 |
| ABCA3 | Pulmonary surfactant dysfunction due to ABCA3 deficiency | BA04838 |
| TSEN54 | Pontocerebellar Hypoplasia | BA04845 |
| ECEL1 | Distal arthrogryposis type 5D | BA04898 |
| MMAB | Methylmalonic Acidemia | BA04899 |
| STXBP2 | Familial hemophagocytic lymphohistiocytosis | BA04900 |
| ASL | Argininosuccinic Aciduria | BA04901 |
| SLC13A5 | Epileptic encephalopathy, early infantile, 25 | BA04902 |
| TBC1D7 | Macrocephaly/megalencephaly syndrome, AR | BA04903 |
| DCAF17 (C2orf37) | Woodhouse-Sakati syndrome | BA04904 |
| NSD1 | Sotos syndrome | BA04905 |
| ABCG5 | Sitosterolemia | BA04913 |
| CLN3 | CLN3 disease | BA04914 |
| SLC2A2 | Fanconi-Bickel syndrome | BA04915 |
| ARSB | Mucopolysaccharidosis type VI | BA04916 |
| WWOX | Spinocerebellar ataxia, AR 12 | BA04917 |
| ACADS | Short-chain acyl-CoA dehydrogenase (SCAD) deficiency | BA04918 |
| TBCE | Kenny-Caffey syndrome type 1 | BA04919 |
| SLC45A2 | Oculocutaneous albinism | BA04920 |
| CYP1B1 | Early-onset glaucoma | BA04921 |
| PTF1A | Pancreatic agenesis 2 | BA04922 |
| BTK | X-linked agammaglobulinemia (XLA) | BA04964 |
| ADA | Adenosine deaminase deficiency | BA04965 |
| DNAI2 | Ciliary dyskinesia, primary, 9 | BA04966 |
| FGA | Hereditary renal amyloidosis | BA04967 |
| BRIP1 | Fanconi Anemia | BA05131 |
| ASPM | Autosomal Recessive Primary Microcephaly (ASPM) | BA05133 |
| KDM6A | Kabuki syndrome | BA05135 |
| ERF | Craniosynostosis | BA05137 |
| KCNT1 | KCNT1-Related Epilepsy | BA05139 |
| TREX1 | Aicardi-Goutières syndrome | BA05141 |
| COL1A2 | Osteogenesis Imperfecta (COL1A2) | BA05143 |
| ALOX12B | Self-healing collodion baby | BA05145 |
| RAG1 | Combined immunodeficiency due to RAG1 deficiency | BA05147 |
| FKRP | FKRP-related muscular dystrophy | BA05154 |
| IDUA | Mucopolysaccharidosis type I (MPS I) | BA05168 |
| POLG | Alpers-Huttenlocher syndrome | BA05170 |
| Deletion 5p | Cri-du-chat syndrome | BA05200 |
| ETFDH | Glutaric acidemia type II | BA05205 |
| GBA | Gaucher disease | BA05206 |
| GJB2 | Nonsyndromic Hearing Loss, DFNB1/DFNA3 | BA05207 |
| KMT2D | Kabuki Syndrome (KMT2D) | BA05208 |
| NPHS2 | Nephrotic syndrome, type 2 | BA05209 |
| RAG2 | Omenn syndrome | BA05210 |
| Deletion 15q11.2 | Deletion 15q11.2 (PWS/AS region) | BA05211 |
| ABCC8, KCNJ11 | Neonatal diabetes mellitus | BA05212 |
| TTR | Transthyretin Amyloidosis | BA05215 |
| GCDH | Glutaric acidemia type I | BA05220 |
| SERPINA1 | Alpha-1 antitrypsin deficiency | BA05233 |
| NPC1 | Niemann-Pick disease (NPC1) | BA05242 |
| BEST1 | Vitelliform macular dystrophy | BA05246 |
| HADHA | Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency | BA05288 |
| UPB1 | Beta-ureidopropionase deficiency | BA05328 |
| FLG | Ichthyosis vulgaris | BA05333 |
| CHRNG | Multiple pterygium syndrome | BA05363 |
| GJA8 | Cataract | BA05364 |
| KRT5 | Epidermolysis bullosa simplex (KRT5) | BA05365 |
| KRT14 | Epidermolysis bullosa simplex (KRT14) | BA05366 |
| MPDZ | Hydrocephalus, congenital, 2 | BA05367 |
| NPPA | Atrial fibrillation, familial | BA05368 |
| PEX2 | Zellweger syndrome (PEX2) | BA05369 |
| PRKG1 | Aortic aneurysm, familial thoracic | BA05370 |
| SLC12A1 | Bartter syndrome type I | BA05371 |
| IKBKG | Incontinentia Pigmenti | BA05536 |
| G6PD | Glucose-6-phosphate dehydrogenase deficiency | BA05547 |
| FANCA | Fanconi Anemia | BA05548 |
| HBB+ HBA 1-2 | Beta thalassemia & Alpha thalassemia | BA05549 |
| PAH | Pulmonary arterial hypertension | BA05550 |
| FGFR2 | Crouzon syndrome | BA05551 |
| MCCC2 | 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency | BA05552 |
| CHEK2 | Susceptibility to breast cancer | BA05683 |
| HFE | Hereditary Hemochromatosis type 1 | BA05684 |
| SCN5A | Long QT syndrome 3 | BA05686 |
| LDLR | Associated disease is Hypercholesterolemia familial 1 | BA05687 |
| FMR1 | Fragile X | BA03816 |
| HPRT1 | Lesch-Nyhan syndrome | BA05685 |
| ATM | Ataxia-Telangiectasia | BA05916 |
| RERE | Neurodevelopmental syndrome | BA05917 |
| AP4M1 | Spastic paraplegia | BA05918 |
| ATXN3 | Spinocerebellar ataxia-3 | BA05919 |
| PKP2 | Arrhythmogenic right ventricular dysplasia 9 | BA05920 |
| KMT2B | Dystonia 28, childhood-onset | BA05921 |
| MYO7A | Deafness, autosomal dominant 11 | BA06027 |
| ADGRG1 | Polymicrogyria, bilateral frontoparietal | BA06030 |
| TNFSF11 | Osteopetrosis, autosomal recessive 2 | BA06032 |
| PPP1R21 | Decreased viability | BA06034 |
| UBA5 | Developmental and epileptic encephalopathy 44 | BA06037 |
| NUBPL | Mitochondrial complex I deficiency, nuclear type 21 | BA06039 |
| SETD5 | Mental retardation, autosomal dominant 23 | BA06041 |
| APRT | Adenine phosphoribosyltransferase deficiency | BA06044 |
| SOX6 | Tolchin-Le Caignec syndrome | BA06046 |
| BCKDHB | Maple syrup urine disease, type Ib | BA06048 |
| GORAB | Geroderma osteodysplasticum | BA06050 |
| TBCK | Hypotonia, infantile, with psychomotor retardation and characteristic facies 3 | BA06052 |
| NDUFS8 | Mitochondrial complex I deficiency, nuclear type 2 | BA06054 |
| NOG | Multiple synostoses syndrome 1 | BA06058 |
| DES | Cardiomyopathy, dilated, 1I | BA06159 |
| ACTA2 | Aortic aneurysm, familial thoracic 6 | BA06160 |
| GCH1 | Dystonia, DOPA-responsive | BA06161 |
| ATRX | Mental retardation-hypotonic facies syndrome, X-linked | BA06162 |
| PNKP | Charcot-Marie-Tooth disease, type 2B2 | BA06163 |
| WNT10A | Odontoonychodermal dysplasia | BA06164 |
| F12 | Hereditary angioedema type 3 | BA06165 |
| Deletion 1q21.1 | 1q21.1 microdeletion | BA06166 |
| AHI1 | Joubert syndrome 3 | BA06167 |
| COL1A1 | Osteogenesis imperfecta | BA06168 |
| CACNA1S | Hypokalemic periodic paralysis, type 1 | BA06169 |
| CACNA1A | Spinocerebellar ataxia 6 (SCA6) | BA06170 |
| dup15q11 | Duplication of 15q 11 region | BA06171 |
| C9orf72 | Frontotemporal dementia and/or ALS 1 | BA06172 |
| ENG | Telangiectasia, hereditary hemorrhagic, type 1 | BA06173 |
| ACVRL1 | Telangiectasia, hereditary hemorrhagic, type 2 | BA06174 |
| MATN3 | Epiphyseal dysplasia, multiple, 5 | BA06180 |
| RASPN | Fetal akinesia deformation sequence 2 | BA06181 |
| CLCN5 | Dent disease 1 | BA06182 |
| F9 | Hemophilia B | BA06183 |
| HEXB | Sandhoff disease, infantile, juvenile, and adult forms | BA06184 |
| ABCG8 | Sitosterolemia 1 | BA06185 |
| GRN | Frontotemporal lobar degeneration with ubiquitin-positive inclusions | BA06186 |
| ATP2A2 | Darier disease | BA06187 |
| MTHFR | Homocystinuria | BA06188 |
| ABCC6 | Pseudoxanthoma elasticum | BA06189 |
| GNPAT | Rhizomelic chondrodysplasia punctata, type 2 | BA06353 |
| SLC6A8 | Cerebral creatine deficiency syndrome 1 | BA06347 |
| ATXN-7 | Spinocerebellar ataxia 7 | BA06348 |
| MICRO DUP | Chromosome 16p11.2 duplication syndrome | BA06349 |
| ATP7B | Wilson disease | BA06350 |
| SNRNP200 | Retinitis pigmentosa 33 | BA06351 |
| MSH6 | Hereditary colorectal cancer | BA06352 |
| SATB2 | Glass syndrome | BA06354 |
| RH | Blood group, RH system | BA06355 |
| DHCR7 | Smith-Lemli-Opitz syndrome | BA06356 |
| RPGR | Retinitis pigmentosa 33 | BA06357 |
| ERCC8 | Cockayne syndrome, type A | BA06358 |
| CNBP | Myotonic dystrophy 2 | BA06360 |
| USH2A | Usher Syndrome, type 2A | BA06361 |
| MLH1 | Mismatch repair cancer syndrome | BA06139 |
| SLC6A8 | Cerebral creatine deficiency syndrome 1 | BA06347 |
| ATXN-7 | Spinocerebellar ataxia 7 | BA06348 |
| 16p11.2 microdup | 16p11.2 microduplication | BA06349 |
| ATP7B | Wilson disease | BA06350 |
| SNRNP200 | Retinitis pigmentosa 33 | BA06351 |
| MSH6 | Hereditary colorectal cancer | BA06352 |
| MTTL1 | MELAS syndrome | BA06362 |
| MLH1 | Mismatch repair cancer syndrome | BA06139 |
| SGCA | Muscular dystrophy, limb-girdle, autosomal recessive 3 | BA06420 |
| COG6 | Congenital disorder of glycosylation, type IIl | BA06424 |
| POMGNT1 | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3 | BA06427 |
| SCN10A | Episodic pain syndrome, familial, 2 | BA06429 |
| POC1A | Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis | BA06433 |
| SH3TC2 | Charcot-Marie-Tooth disease, type 4C | BA06435 |
| GBE1 | Glycogen storage disease IV | BA06438 |
| KIF1C | Spastic ataxia 2, autosomal recessive | BA06440 |
| DNAH11 | Ciliary dyskinesia, primary, 7, with or without situs inversus | BA06442 |
| B3GALNT2 | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11 | BA06444 |
| ZFYVE26 | Spastic paraplegia 15, autosomal recessive | BA06447 |
| SLC26A4 | Deafness, autosomal recessive 4, with enlarged vestibular aqueduct | BA06449 |
| POLD1 | Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome | BA06453 |
| SLC12A3 | Gitelman syndrome | BA06455 |
| DEAF1 | Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures | BA06458 |
| PEX1 | Peroxisome biogenesis disorder 1A (Zellweger) | BA06500 |
| TMEM216 | Joubert syndrome 2 / Meckel syndrome 2 | BA06501 |
| TTN | Dilated Cardiomyopathy 1G | BA06502 |
| MYL2 | Hypertrophic Cardiomyopathy 10 | BA06503 |
| GAA | Glycogen storage disease II | BA06504 |
| BBS1 | Bardet-Biedl syndrome 1 | BA06505 |
| CLDN19 | Hypomagnesemia 5, renal, with ocular involvement | BA06506 |
| CPABPN1 | Oculopharyngeal muscular dystrophy | BA06507 |
| BTD | Biotinidase deficiency | BA06508 |
| SERPING1 | Angioedema, hereditary, 1 and 2 | BA06509 |
| PCNT | Microcephalic osteodysplastic primordial dwarfism, type II | BA06510 |
| WNT2B | Diarrhea 9 | BA06511 |
| ATAD3A | Harel-Yoon syndrome | BA06512 |
| COL3A1 | Ehlers-Danlos syndrome, vascular type | BA06513 | ELANE | Neutropenia, severe congenital 1 | BA06514 | ADAR | Aicardi-Goutieres syndrome 6 | BA06637 | F5 | Factor V deficiency | BA06638 | CBS | Homocystinuria | BA06639 | Xq21.1 | Chrosome Xq21.1 duplication syndrome | BA06640 | MEFV | Familial Mediterranean fever | BA06641 | TMEM67 | Joubert syndrome 6 | BA06643 | PIGT | Multiple congenital anomalies-hypotonia-seizures syndrome 3 | BA06644 | CAPN3 | Muscular dystrophy, limb-girdle | BA06645 | 16p13.11 | Chrosome 16p13.11 duplication syndrome | BA06646 | SLC37A4 | Glycogen storage disease I | BA06647 | FLCN | Birt-Hogg-Dube syndrome | BA06648 | SLC26A2 | Diastrophic dysplasia | BA06649 | DUOX2 | Thyroid dyshormonogenesis 6 | BA06650 | PAX9 | Tooth agenesis, selective, 3 | BA06651 | PLA2G6 | Neurodegeneration with brain iron accumulation 2B | BA06652 | CRB1 | Retinitis pigmentosa | BA06653 | GJB1 | Charcot-Marie-Tooth neuropathy 1 | BA06654 |
Custom designs available upon request.
Featured PGD-SEQ solutions:
- SMN1 Panel and Reagent Kit for spinal muscular atrophy (SMA)
- CFTR Panel and Reagent Kit for cystic fibrosis
- COL1A1 Panel and Reagent Kit for osteogenesis imperfecta
- FMR1 Panel and Reagent Kit for fragile X
- HBA1/HBA2 Panel and Reagent Kit for alpha thalassemia
- HBB Panel and Reagent Kit for beta thalassemia
Learn about PGT from key opinion leaders in the field
Recent Advances for Simultaneous Analysis, to Determine Embryo PGT-A and PGT-M Status with NGS
Cengiz Cinnioglu, PhD
Founder & CEO, NextGen Genetics
Simplified preimplantation genetic testing workflow on a single embryo biopsy
Luis Alcaraz, PhD
Co-founder, Scientific and Laboratory Director
Bioarray
Simultaneously research PGT-A and PGT-M in the same NGS workflow from a single sample
Combine the PGD-SEQ kit with Ion ReproSeq PGS kit using the Ion GeneStudio S5 System for a simple, scalable and automated sample-to-answer workflow solution that includes PGT-M and PGT-A results from single research sample.
Learn more ›
PGT-M Ordering Information
Consult an expert about how to bring simple, scalable and automated NGS to your lab, or inquire about the latest genes available for PGT-M.
For Research Use Only. Not for use in diagnostic procedures.
* PGD-SEQ is a trademark of Bioarray, S.L.
For Research Use Only. Not for use in diagnostic procedures.