baylor college of medicine antibody test

“The challenge is to not to mistake previous coronavirus infections — common, milder — for the new coronavirus.”. It followed a report by more than 50 scientists that found just three of every 14 coronavirus antibody tests provide consistently reliable results. Here’s the problem. We are following the state guidelines for distributing the COVID-19 vaccine and have offered vaccine appointment slots to all of our interested Phase 1A employees and learners. First, the school must secure funding — easy, says Klotman — then design unbiased studies, not so easy, given that people those who’ve experienced some symptoms and suspect they may have had COVID-19 are more likely to volunteer. UAB is working with Gilead Sciences and nearly a dozen other universities across the U.S. as part of a five-year $37.5 million grant from the National Institute of Allergy and Infecti… Request Quote. The survey has been awaited since Baylor College of Medicine confirmed in late May that its COVID-19 antibody test was highly accurate and could be deployed in the area. meaning it produced false negatives 10 percent of the time. $ 265. Dr. Peter Hotez, an infectious disease expert at the Baylor College of Medicine in Houston, questioned the value of antibody tests at this point in the pandemic. Such antibody testing, repeated over time, also would show the area’s progress toward herd immunity, the protection from a contagious disease that occurs when a high percentage of the population has either had the infection or been vaccinated. Baylor Genetics assumes no responsibility for billing errors due to reliance on the CPT codes listed. But most were unreliable, it turned out. Those tests are not as far along in development. The Houston Health Department is now rolling out its own antibody testing survey, in conjunction with the Centers for Disease Control and Prevention, Rice University and Baylor College of Medicine. (Michael Ciaglo / Houston Chronicle). RELATED: Coronavirus antibody tests have proliferated in San Antonio. Antibody testing will help determine the extent of community spread. After months of emphasis on diagnostic screening, contact tracing and research into possible treatments, Houston is about to deploy a new tool in the effort to contain COVID-19: antibody testing. Enthusiasm for antibody testing’s role in reopening the country has waned not just because of the tests’ unreliability but because the number of people with ostensible immunity is far too small to affect necessary workplace social distancing. The FDA, under fire for allowing the marketing of the tests, earlier this month stepped up its scrutiny, requiring that companies submit data proving their accuracy. Klotman said he anticipates Baylor will partner with local health departments to determine optimal resource allocation — such as where to focus testing and contact tracing — based on the prevalence the studies find in communities. From there, Baylor can hone in on the areas where infection rates are highest. Similar testing … Baylor College of Medicine. Baylor College of Medicine is committed to vaccinating our patients as quickly as we can. If you’re an established patient and experiencing symptoms of COVID-19 call (713) 798-3888 for evaluation. It's well known that antibodies wane, but T cells have immunological memory," said Dr. Peter Hotez, an infectious disease specialist at Baylor College of Medicine. CPT coding is the sole responsibility of the billing party. Baylor Medicine is currently testing patients who have established care in our clinics and based on CDC testing criteria. Harris County Public Health Department Executive Director and Dr. Umair Shah speaks about the contact tracer army during a press conference Wednesday, May 13, 2020, in Houston. Dr. Pedro Piedra's CLIA certified laboratory at BCM is developing a serological test to identify recent or past infections with SARS-CoV-2, the virus that causes Coronavirus Disease 2019 (COVID-19). Here’s the problem. Baylor College of Medicine to use antibody testing to determine COVID-19's prevalence in Houston Houston Chronicle | 05-26 After months of emphasis on diagnostic screening, contact tracing and research into possible treatments, Houston is about to deploy a new tool in the effort to contain COVID-19: antibody testing. This partnership is currently conducting a placebo-controlled trial that will test the safety and effectiveness of the anti-viral drug Remdesivir. Even the best are flawed, it found. COVID-19 Resources for Test Developers Emergency Use Authorizations for Medical Devices : Includes EUAs for In Vitro Diagnostics (e.g., molecular, antigen, and serology tests) It is now separating the two. Baylor College of Medicine researchers Thursday presented evidence to school leadership that the blood test it developed to detect whether an individual has been infected with the coronavirus is highly accurate and thus ready for use in studies assessing the virus’ reach in the area. “Everything you hear is that the virus is ravaging communities of color, people at high risk,” said Klotman. One partnership that has been examining the development of anti-viral drugs against SARS-CoV-2 is the partnership between University of Alabama (UAB) and the pharmaceutical manufacturer, Gilead. The lab’s results presented this week: the Baylor test correctly ruled out people who had not had the infection 99 percent of the time, meaning it produced false positives 1 percent of the time; it correctly identified people who have been infected 90 percent of the time. ... Baylor College of Medicine to use antibody testing to determine COVID-19’s prevalence in Houston. CL1000 production (100-mg scale) Request Quote. LOCKED INSIDE: An outbreak at the county jail was a nightmare scenario — then it happened. The Houston Health Department, in partnership with Rice University’s Kinder Institute, Baylor College of Medicine, and the Centers for Disease Control and Prevention, is … Who is Baylor Medicine testing for COVID-19? Baylor to use antibody testing to determine prevalence of COVID-19 in Houston Vasanthi Avadhanula shows Dr. Pedro Piedra lab results from Baylor College of Medicine’s work with antibodies … GeneAware ACMG/ACOG Panel Version 2 (Female), GeneAware ACMG/ACOG Panel Version 2 (Male), GeneAware Ashkenazi Jewish Panel Version 2 (Female), GeneAware Ashkenazi Jewish Panel Version 2 (Male), GeneAware Complete Panel Version 2 (Female), GeneAware Complete Panel Version 2 (Male), 11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP11B1), 17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP17A1), 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD17B10), 3 - Methylcrotonyl-CoA Carboxylase Deficiency - MCCC1 Related, 3 - Methylcrotonyl-CoA Carboxylase Deficiency - MCCC2 Related, 3-Methylcrotonyl-CoA Carboxylase Deficiency Panel (MCCC1, MCCC2), Acetyl-CoA Carboxylase Deficiency (ACACA), Acute Recurrent Myoglobinuria - LPIN1 Related, Acyl-CoA Dehydrogenase 9 Deficiency (ACAD9), Acyl-CoA Dehydrogenase, Short/Branched Chain Deficiency (ACADSB), Adenine Phosphoribosyltransferase Deficiency (APRT), Agenesis of the Corpus Callosum with Peripheral Neuropathy, Aggressive/High-Grade B-Cell Lymphoma Panel, Amino Acid Analysis - Cerebrospinal Fluid, Arginine: Glycine Amidinotransferase (GATM) Deficiency (AGAT), Arylsulfatase A Deficiency [Metachromatic Leukodystrophy], Ataxia with Isolated Vitamin E Deficiency, Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (APTX), Bardet-Biedl Syndrome (18 gene panel by NGS), B-Cell Clonality Screening (IgH and IgK) by PCR, BCR-ABL1 Mutation Analysis for Tyrosine Kinase Inhibitor Resistance by Next Generation Sequencing, BCR-ABL1, Qualitative Analysis with Reflex to BCR-ABL1 Quantitative, Bile acid synthesis defect, congenital, 2 (AKR1D1), BRCA1 Related Disorders; BRCA 2 Related Disorders, CALR (Calreticulin) Exon 9 Mutation Analysis by PCR, Cancer Chromosomal Microarray Analysis - 180K CGH/SNP Array, Carbamoyl Phosphate Synthetase Deficiency (CPS1), Carnitine Acylcarnitine Translocase (CACT) Deficiency (SLC25A20 ), Carnitine Deficiency, Systemic (SLC22A5 (OCTN2)), Carnitine Palmitoyltransferase IA Deficiency (CPT1A ), Carnitine Palmitoyltransferase II Deficiency (CPT2), Cholestasis Panel by NGS (7 gene panel by NGS), Chondrodysplasia punctata, rhizomelic, type 2 (GNPAT), Chromosomal Microarray Analysis - HR + SNP Screen (Comprehensive), Chromosome Analysis - Prenatal - Amniotic Fluid, Chromosome Analysis - Prenatal - Amniotic Fluid with ACHE, Chromosome Analysis - Prenatal - Amniotic Fluid with AFP, CMA-Expanded and Limited Karyotype - Prenatal - Amniotic Fluid, CMA-Expanded and Limited Karyotype - Prenatal - CVS, CMA-Targeted and Limited Karyotype - Prenatal - Amniotic Fluid, CMA-Targeted and Limited Karyotype - Prenatal - CVS, Cobalamin Metabolism Panel (20 gene panel by NGS), Coenzyme Q10 Deficiency - CABC1 (ADCK3) Related, Coenzyme Q10 Deficiency - COQ2 Related (COQ2, CL640, FLJ26072), Coenzyme Q10 Deficiency - PDSS2 Related (PDSS2, bA59I9.3), COL1A1/2 Related Disorders (2 gene panel by NGS), Combined Malonic & Methylmalonic Aciduria (ACSF3), Combined Oxidative Phosphorylation Deficiency - TSFM Related (EF-TS, EF-Tsmt), Combined Oxidative Phosphorylation Deficiency 1 (GFM1), Combined Oxidative Phosphorylation Deficiency 10, Combined Oxidative Phosphorylation Deficiency 12, Combined Oxidative Phosphorylation Deficiency 5 (MRPS22), Combined Oxidative Phosphorylation Deficiency 7 (C12orf65), Combined Oxidative Phosphorylation Deficiency 8 (AARS2), Combined Oxidative Phosphorylation Deficiency 9, Common Hereditary Cancer Panel (27 gene panel by NGS), Comprehensive Autism Panel - Female Specific, Comprehensive Autism Panel - Male Specific, Comprehensive Hereditary Cancer Panel (61 gene panel by NGS), Congenital Disorder of Glycosylation, Type Ic (ALG6), Congenital Disorder of Glycosylation, Type Id (ALG3), Congenital Disorder of Glycosylation, Type If, Congenital Disorder of Glycosylation, Type Ig (ALG12), Congenital Disorder of Glycosylation, Type Ih (ALG8), Congenital Disorder of Glycosylation, Type IIb, Congenital Disorder of Glycosylation, Type IIc, Congenital Disorder of Glycosylation, Type IId (B4GALT1), Congenital Disorder of Glycosylation, Type IIe, Congenital Disorder of Glycosylation, Type IIf, Congenital Disorder of Glycosylation, Type IIg, Congenital Disorder of Glycosylation, Type IIh, Congenital disorder of glycosylation, type IIi (COG5), Congenital disorder of glycosylation, type IIj (COG4), Congenital disorder of glycosylation, type IIk (TMEM165), Congenital Disorder of Glycosylation, Type IIm (SLC35A2), Congenital Disorder of Glycosylation, Type Il (ALG9), Congenital disorder of glycosylation, type Ip (ALG11), Congenital disorder of glycosylation, type Ir (DDOST), Congenital Disorder of Glycosylation, Type Iv (NGLY1), Congenital Disorders of Glycosylation - CDG Panel (36 gene panel by NGS), Congenital Disorders of Glycosylation (TUSC3), Congenital Disorders of Glycosylation MPI Related, Congenital Disorders of Glycosylation PMM2 Related, Congenital Disorders of Glycosylation Type Ik, Congenital Disorders of Glycosylation Type Im (DOLK), Congenital Ichthyosis Autosomal Recessive 1, Coronary Heart Disease Risk Factor (9p21 rs10757278), Creatine and Guanidinoacetate Determination - Plasma, Creatine and Guanidinoacetate Determination - Urine, Creatine Transporter Deficiency - SLC6A8 Related, Deafness-Dystonia-Optic Neuronopathy Syndrome - TIMM8A, Developmental Glaucoma (8 gene panel by NGS), Dual Genome Leigh Disease (128 gene panel by NGS), EGFR Mutation Detection by Pyrosequencing, Ehlers-Danlos Syndrome Types III & IV (COL3A1), Ehlers-Danlos Syndrome, Classic Type - COL5A1 Related, Ehlers-Danlos Syndrome, Classic Type - COL5A2 Related, Ehlers-Danlos Syndrome, Kyphoscoliotic Form - PLOD1 Related, EIF2B5 - Related Leukoencephalopathy with Vanishing White Matter, Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission (DNM1L), Epileptic Encephalopathy, Early Infantile, 4, Expanded Chromosomal Microarray Analysis - Prenatal - Amniotic Fluid, Expanded Chromosomal Microarray Analysis - Prenatal - CVS, Familial Exudative Vitreoretinopathy (4 gene panel by NGS), Familial Thrombocytopenia with Propensity to Acute Myelogenous Leukemia, Fanconi Anemia Complementation Group N (PALB2), Fanconi Anemia Complementation Group O (RAD51C), Fatty Acid Oxidation Deficiency (22 gene panel by NGS), FISH Analysis - Charcot-Marie-Tooth Neuropathy Type 1A, FISH Analysis - Chromosome X and Y Centromere Analysis, FISH Analysis - Custom Familial FISH Studies, FISH Analysis - DiGeorge/Velocardiofacial Syndrome Panel (22q and 10p), FISH Analysis - DiGeorge/Velocardiofacial Syndrome Type I (22q), FISH Analysis - Hereditary Neuropathy with Liability to Pressure Palsies, FISH Analysis - Langer-Giedion Syndrome Panel (EXT1 and TRPS1), Fructose 1,6 Bisphosphatase Deficiency (FBP1), Global Metabolomic Assisted Pathway Screen (Global MAPS), Glucose Transporter Type 1 Deficiency Syndrome, Glycogen Storage Disease Type 0, Liver Isoform (GYS2), Glycogen Storage Disease Type 0, Muscle Isoform (GYS1), Glycogen Storage Disease Type I (b,c,d) (SLC37A4), Glycogen Storage Disease Type Ia (G6PC , GSD1a), Glycogen Storage Disease Type IX - PHKA1 Related, Glycogen Storage Disease Type IX - PHKA2 Related, Glycogen Storage Disease Type IX - PHKB Related, Glycogen Storage Disease Type IX - PHKG2 Related, Glycogen Storage Disease Type XIII (ENO3), Glycogen Storage Disorder - Comprehensive Panel (23 gene panel by NGS), Glycogen Storage Disorder - Liver Panel by NGS (13 gene panel by NGS), Glycogen Storage Disorder - Muscle Panel by NGS (13 gene panel by NGS), Guanidinoacetate Methyltransferase Deficiency (GAMT), Gyrate Atrophy of Choroid and Retina (OAT), Hereditary Brain/CNS/PNS Cancer Panel (17 gene panel by NGS), Hereditary Breast/Ovarian/Endometrial Cancer Panel (23 gene panel by NGS), Hereditary Colorectal/Gastrointestinal Cancer Panel (22 gene panel by NGS), Hereditary Endocrine Cancer Panel (15 gene panel by NGS), Hereditary Hearing Loss and Deafness - GJB2 Related, Hereditary Hearing Loss and Deafness - GJB6 Related, Hereditary Hemorrhagic Telangiectasia Type 1 (ENG), Hereditary Leukemia/Lymphoma Panel (13 gene panel by NGS), Hereditary Melanoma Panel (4 gene panel by NGS), Hereditary Neuralgic Amyotrophy (HNA) (SEPT9), Hereditary Pancreatic Cancer Panel (16 gene panel by NGS), Hereditary Paraganglioma/Pheochromocytoma Panel (9 gene panel by NGS), Hereditary Prostate Cancer Panel (5 gene panel by NGS), Hereditary Renal Cancer Panel (12 gene panel by NGS), HFE - Associated Hereditary Hemochromatosis, High Risk Hereditary Breast Cancer Panel (7 gene panel by NGS), High Risk Hereditary Colorectal Cancer Panel (12 gene panel by NGS), Holocarboxylase Synthetase Deficiency (HLCS , HCS), Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (CBS), Hyperinsulinism-Hyperammonemia Syndrome (GLUD1), Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency (AHCY), Hypophosphatemic Nephrolithiasis/Osteoporosis, 1 (SLC34A1), Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 2, Intrahepatic Cholestasis - ABCB11 Related, Intrahepatic Cholestasis - ATP8B1 Related, Isobutyryl-CoA Dehydrogenase Deficiency (ACAD8), KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy, Ketotic Hypoglycemia and Gluconeogenesis Panel (ALDOB, FBP1, GYS2, PC), KIT Mutations in AML by Fragment Analysis and Sequencing, Leber Congenital Amaurosis Panel (19 gene panel by NGS), Leber Congenital Amaurosis, Calcium Binding Protein 4 Deficiency (CABP4), Leber Congenital Amaurosis, IQ Motif Containing B1 Deficiency (IQCB1), Leukoencephalopathy with dystonia and motor neuropathy (SCP2), Low Bone Mass Panel by NGS (23 gene panel by NGS), Maple Syrup Urine Disease (4 gene panel by NGS), Maple Syrup Urine Disease Type 1A (BCKDHA), Maple Syrup Urine Disease Type 1B (BCKDHB), Maturity-Onset Diabetes of the Young (MODY) (25 gene panel by NGS), Megalencephalic Leukoencephalopathy with Subcortical Cysts, Methylcobalamin Deficiency, cblG Type (MTR), Methylmalonic Acidemia - 3 Gene Panel (MUT, MMAA, MMAB), Methylmalonic Acidemia - MMAA Related (cblA), Methylmalonic Acidemia - MMAB Related (cblB), Methylmalonic Acidemia and Homocysteinemia, cblX Type (HCFC1), Methylmalonic Aciduria due to Transcobalamin Receptor Defect (CD320), Microphthalmia, Isolated 5 Disorder (MFRP), Microsatellite Instability (MSI), HNPCC/Lynch Syndrome, by PCR, Mitchondrial Complex III Deficiency - UQCR10 Related, Mitochondrial Complex I Deficiency - NDUFB8 Related, Mitochondrial Complex I Deficiency-FOXRED1 Related, Mitochondrial Complex I Deficiency-NDUFA11 Related, Mitochondrial Complex I Deficiency-NDUFAF3 Related, Mitochondrial Complex I Deficiency-NUBPL Related, Mitochondrial Complex II Deficiency, SDHAF1 Related, Mitochondrial Complex III Deficiency Nuclear Type 5, Mitochondrial Complex III Deficiency-TTC19 Related, Mitochondrial Complex IV Deficiency-COX4I1 Related, Mitochondrial Complex IV Deficiency-TACO1 Related, Mitochondrial Complex V Deficiency - ATP5O Related, Mitochondrial Complex V Deficiency-ATP5E Related, Mitochondrial Depletion Syndrome Panel (20 gene panel by NGS), Mitochondrial Disorders - MTHFD1L Related, Mitochondrial DNA Content (qPCR) Analysis - Liver, Mitochondrial DNA Content (qPCR) Analysis - Skeletal Muscle, Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) (FBXL4), Mitochondrial DNA Depletion Syndrome SUCLG2-Related, Mitochondrial DNA Point Mutations and Deletions-NGS, Mitochondrial Genome Comprehensive Analysis, Mitochondrial Myopathy and Sideroblastic Anemia Type 1 (PUS1), Mitochondrial Myopathy and Sideroblastic Anemia Type 2 (YARS2), Mitochondrial Nonsyndromic Hearing Loss and Deafness Mutation Panel, Mitochondrial Respiratory Chain Complex I Deficiency (25 nuclear gene panel by NGS), Mitochondrial Respiratory Chain Complex II Deficiency (6 nuclear gene panel, Mitochondrial Respiratory Chain Complex III Deficiency (4 nuclear gene panel by NGS), Mitochondrial Respiratory Chain Complex IV Deficiency (12 nuclear gene panel by NGS), Mitochondrial Respiratory Chain Complex I-V Deficiency (50 nuclear gene pan, Mitochondrial Respiratory Chain Complex V Deficiency (3 nuclear gene panel by NGS), Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skeletal Muscle, Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skin Fibroblasts, Mitochondrial/Metabolic (MitoMet®Plus) Microarray Analysis, Mitome200-Dual Genome Panel by NGS (229 gene panel by NGS), Mitome200-Nuclear Gene Panel by NGS (192 gene panel by NGS), Modifier of Bardet-Biedl syndrome (CCDC28B), Molybdenum Cofactor Deficiency - MOCS1 Related, Molybdenum Cofactor Deficiency - MOCS2 Related, MPL codon 515 Mutation Detection by Pyrosequencing, Quantitative, Mucopolysaccharidosis Type IIIA (Sanfilippo A), Multiple Acyl-CoA Dehydrogenase Deficiency - ETFA Related, Multiple Acyl-CoA Dehydrogenase Deficiency - ETFB Related, Multiple Acyl-CoA Dehydrogenase Deficiency - ETFDH Related, Multiple Acyl-CoA Dehydrogenase Deficiency Panel (ETFA, ETFB & ETFDH), MYD88 L265P Mutation Detection by PCR, Quantitative, Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay (GFER), Myopathy/Rhabdomyolysis Panel by NGS (25 gene panel by NGS), N-Acetylglutamate Synthase Deficiency (NAGS), Niemann-Pick Disease Type C - NPC1 Related, Niemann-Pick Disease Type C - NPC2 Related, Nonsyndromic Hearing Loss and Deafness, X-Linked - POU3F4 Related, Noonan Spectrum Disorders (12 gene panel by NGS), NRAS Mutation Detection by Pyrosequencing, Nuclear Encoded ATPase Deficiency, TMEM70 Related, Nuclear Encoded Complex I Deficiency - NDUFA1 Related (CI-MWFE, MWFE), Nuclear Encoded Complex I Deficiency - NDUFAF1 Related, Nuclear Encoded Complex I Deficiency - NDUFAF2 Related (B17.2L, MMTN), Nuclear Encoded Complex I Deficiency - NDUFS3 Related, Nuclear Encoded Complex I Deficiency - NDUFS4 Related, Nuclear Encoded Complex I Deficiency - NDUFS6 Related, Nuclear Encoded Complex I Deficiency - NDUFS8 Related, Nuclear Encoded Complex I Deficiency - NDUFV1 Related, Nuclear Encoded Complex I Deficiency-NDUFS1 Related, Obesity, Monogenic Nonsyndromic - LEP Related, Obesity, Monogenic Nonsyndromic - LEPR Related, Obesity, Monogenic Nonsyndromic - PCSK1 Related, Obesity, Monogenic Nonsyndromic - POMC Related, Oncology Chromosome Analysis - Solid Tumor, Oncology Chromosome Analysis-Hematologic Cancer, Oncology FISH Analysis - All Pediatric FISH Panel, Oncology FISH Analysis - AML1/ETO(RUNX1/RUNX1T1): t(8;21) [AML], Oncology FISH Analysis - BCL2 Rearrangement, Oncology FISH Analysis - BCL6 Rearrangement, Oncology FISH Analysis - BCR/ABL: t(9;22) [CML/ALL/AML], Oncology FISH Analysis - CBFB: inv(16) [AML], Oncology FISH Analysis - CHIC2: Deleted 4q [Hypereosinophilic Syndrome], Oncology FISH Analysis - Deletion 20q12 [MDS], Oncology FISH Analysis - Deletion 5 [MDS], Oncology FISH Analysis - Deletion 7 [MDS], Oncology FISH Analysis - Eosinophilia FISH Panel, Oncology FISH Analysis - ERBB2 (HER2/neu), Oncology FISH Analysis - Gain Chromosome 8, Oncology FISH Analysis - IGH Rearrangement, Oncology FISH Analysis - IGH/BCL2: t(14;18) [Follicular Lymphoma], Oncology FISH Analysis - IGH/CCND1: t(11;14) [Mantle Cell Lymphoma], Oncology FISH Analysis - MET Amplification, Oncology FISH Analysis - Multiple Myeloma FISH Panel, Oncology FISH Analysis - MYC translocation, Oncology FISH Analysis - RET Rearrangement, Oncology FISH Analysis - ROS1 Rearrangement, Oncology FISH Analysis - SS18 FISH for Synovial Sarcoma, Oncology FISH Analysis - TCF3/PBX1 FISH for ALL, Oncology FISH Analysis - TEL/AMLI: t(12;21) [ALL], Oncology FISH Analysis- Multiple Myeloma IgH Rearrangement FISH Panel, OPA3 - Related Disorders (FLJ22187, MGA3), Ornithine Transcarbamylase Deficiency (OTC), Osteopathia Striata with Cranial Sclerosis, Osteopetrosis with Renal Tubular Acidosis (CA2), PCDH19 - Related X-Linked Female-Limited Epilepsy w/MR, PDH & Mitochondrial Respiratory Chain Complex V Deficiency (9 nuclear gene panel by NGS), PD-L1 22C3 IHC for NSCLC by Immunohistochemistry with Interpretation, Pembrolizumab (KEYTRUDA), PD-L1 22C3 IHC with Combined Positive Score (CPS) Interpretation, pembrolizumab (KEYTRUDA), PD-L1 28-8 pharmDx by Immunohistochemistry with Interpretation, nivolumab (OPDIVO), Peroxisomal acyl-CoA oxidase deficiency (ACOX1), Peroxisomal Disorders (22 gene panel by NGS), Peroxisome Biogenesis Disorder 10A (Zellweger) (PEX3), Peroxisome Biogenesis Disorder 11 (PEX13), Peroxisome Biogenesis Disorder 12A (Zellweger) (PEX19), Peroxisome Biogenesis Disorder 13A (Zellweger) (PEX14), Peroxisome Biogenesis Disorder 14B (PEX11B), Phenylalanine Hydroxylase Deficiency (PAH), PHEO and PGL Syndrome Panel (SDHB, SDHC, & SDHD), Phosphoenolpyruvate carboxykinase-1, cytosolic, deficiency (PCK1), PML-RARA Translocation, t(15;17) by RT-PCR, Quantitative, Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Disorder (ABHD12), Pontocerebellar Hypoplasia Type 6 (RARS2), Prader-Willi-like Syndrome; Intellectual Disability; Autism (MAGEL2), PreSeek Non-invasive Prenatal Gene Sequencing Screen, Primary Open Angle Glaucoma (2 gene panel by NGS), Progressive External Ophthalmoplegia - PEO Panel (10 gene panel by NGS), Proximal Urea Cycle Disorders (3 gene panel by NGS), Pyruvate Dehydrogenase E2 Deficiency (DLAT), Pyruvate Dehydrogenase E3-Binding Protein (Component X) Deficiency (PDHX), Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1), Rapid FISH Analysis - AneuVysion® (+13/+18/+21 /X/Y), Rapid FISH Analysis - Sex Chromosome (X/SRY), Recessive Intermediate D Charcot-Marie-Tooth Disease, Retinitis Pigmentosa Panel (66 gene panel by NGS), Retinitis Pigmentosa, Autosomal Recessive, Bothnia Type (RLBP1), Rhizomelic chondrodysplasia punctata, type 3 (AGPS), Rubinstein-Taybi Syndrome - CREBBP Related, Severe Combined Immunodeficiency, Athabascan Type, Severe Combined Immunodeficiency, Autosomal Recessive, T- Negative/B-Positive Type, Severe Combined Immunodeficiency, B Cell-Negative, Spastic Paraplegia 7, Autosomal Recessive (SPG7), Spondylocheirodysplasia, Ehlers-Danlos Syndrome (SLC39A13), Succinic Semialdehyde Dehydrogenase Deficiency (ALDH5A1), Targeted Chromosomal Microarray Analysis - Prenatal - Amniotic Fluid, Targeted Chromosomal Microarray Analysis - Prenatal - CVS, Targeted mtDNA Analysis by Massively Parallel Sequencing (MitoNGS, Tay-Sachs Disease Carrier Testing (Serum), TAZ - Related Disorders (BTHS, G4.5, XAP-2), TCIRG1-Related Autosomal Recessive Osteopetrosis, Trifunctional Protein Deficiency Panel (HADHA & HADHB), Urea Cycle Disorders and Hyperammonemia (8 gene panel by NGS), X-Linked Severe Combined Immunodeficiency (IL2RG). 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