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… “That’s needed to better understand how infections impact different Houston communities, the variations in those communities and the numbers in certain high-risk environments, like prisons and nursing homes.”. Larry H. Taber's research while affiliated with Baylor College of Medicine and ... the amount of antibody transmitted to the infant and postpone the need for active immunization. Both Baylor and Houston Methodist Hospital, which has also developed an antibody test, are working on tests that measure the level of antibodies, not just whether there is or isn’t a presence of them. At Baylor Scott & White Health, there is nothing more important to us than the well-being of our patients and staff and the broader health of our communities. 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. 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. The promise of the test, a prick of the finger seemingly all that’s necessary to show an individual has immunity, triggered an onslaught of entrepreneurial activity in the United States. Baylor Medicine is currently testing patients who have established care in our clinics and based on CDC testing criteria. Show full articles without "Continue Reading" button for {0} hours. Troisi argues that immunity passports — the idea of digital or physical documents that certify an individual has been infected and is purportedly immune — likely would lead to black markets and workplace discrimination and privacy concerns. Similar testing … Baylor College of Medicine. Baylor Genetics strongly recommends that clients confirm CPT/HCPCS codes with their Medicare Administrative Contractor (MAC) or other payer being billed, as requirements may differ. The emerging consensus for now is antibody tests’ great value is population studies and public health planning, the work that Baylor hopes to start soon. 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. 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. A Baylor prevalence study based on antibody testing would put the Houston region among a handful of U.S. communities to conduct such research, which has found that more than 20 percent of people in New York City but only 4 percent of those in Los Angeles County have been infected. Vasanthi Avadhanula shows Dr. Pedro Piedra lab results from Baylor College of Medicine’s work with antibodies to the coronavirus. But even when antibodies are correctly identified, some experts warn against assuming too much. Dr. Pedro Piedra, a professor at the Baylor College of Medicine, weighs in. “This will tell us the severity of the disease based on prevalence, the number of people who have had the virus but do not show up in case counts because they were asymptomatic and weren’t tested,” said Dr. Paul Klotman, president of Baylor. The HCPHD currently has about 50 contact tracers and the agency is aiming to have 200 by the end of the week, and have 300 contact tracers next week. 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. Duncan Cancer Center. In Sept., teams from HHD’s staff and the Houston Fire Department paramedics will visit randomly selected homes to perform a COVID-19 antibody test . ... Baylor College of Medicine to use antibody testing to determine COVID-19’s prevalence in Houston. A monthslong study to determine the number of Houstonians carrying COVID-19 antibodies revealed infections may have been four times greater than viral tests showed, according to collaborators at the Houston Health Department, Rice University and Baylor College of Medicine. The tests were originally touted as a tool to guide the reopening of the economy and the reintegration of society, based on the hope the presence of antibodies in individuals confers immunity to COVID-19, allowing them to interact with others without the risk of passing on or contracting the virus. Even the Texas department of health was guilty, until recently including positive antibody tests in coronavirus case counts. Coronavirus antibody tests have proliferated in San Antonio. It was because of the lack of accurate tests that Baylor developed its own in recent months, first using it to confirm the presence of antibodies in blood plasma donated by people who had recovered from COVID-19 as possible therapy for the disease, ultimately having a laboratory that validates the flu test every year verify its reliability. 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. “We think that’s true, but what we don’t know is if those communities have more virus than other communities. Baylor Genetics assumes no responsibility for billing errors due to reliance on the CPT codes listed. After a person has been infected with SARS-CoV-2, they will typically develop antibodies within seven to 10 days, Joseph F. Petrosino, PhD, chairman of the Department of Molecular Virology and Microbiology at the Baylor College of Medicine, tells Verywell. 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 … Baylor College of Medicine confirmed in late May that its COVID-19 antibody test was highly accurate and could be deployed in the area. We have been continuously evaluating opportunities to build additional capacity in our hospitals in anticipation of future needs related to the treatment of patients diagnosed with COVID-19. Dr. Umair Shah, executive director of Harris County Public Health, expresses concern that “the unfettered COVID-19 antibody testing being shopped around by vendors” has fueled confusion — some have used it as a diagnostic tool, though even reliable tests only show that the body has mounted a defense against the virus, not whether there’s active virus at that moment. 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. 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) Those tests are not as far along in development. 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. Request Quote. Klotman said he thinks Houston’s rate will be closer to the California number. $ 265. 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. Still, Klotman envisions a study testing the blood of about 5,000 people reflective of the area’s diverse demographics, selected by ZIP code. 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). 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. Christus Health, which operates hospitals in Texas, bought about 70,000 kits made by a Houston-based manufacturer in March — the test isn’t one of the 13 the FDA has approved — but the system has no hospital in the Houston area. With Baylor Medicine Telehealth 24/7, you can access a board-certified emergency medicine physician in minutes. Baylor to use antibody testing to determine prevalence of COVID-19 in Houston, © Brett Coomer, Houston Chronicle / Staff Photographer, © Yi-Chin Lee, Houston Chronicle / Staff Photographer, © Michael Ciaglo, Staff Photographer / Houston Chronicle. If your home is selected, please participate! "Within a period of a week or so, we are going to have a rather large number of tests that are available," said Dr. Fauci. Experts say that percentage — there is no vaccine for the coronavirus yet — needs to reach at least 60 to 70. 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. The test is free for those patients with verified health insurance coverage. If you’re an established patient and experiencing symptoms of COVID-19 call (713) 798-3888 for evaluation. 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 launching a … 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. 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. Because so little is known about the virus, they question how long antibodies confer protection — or even if they confer protection. CL1000 production (100-mg scale) Request Quote. “We may not detect all individuals who’ve been infected but the goal is as few false positives as possible,” Pedro Piedra, a Baylor professor of molecular virology and microbiology and the leader of the research, said during the test’s development. Piedra led Baylor’s development of a coronavirus antibody blood test the medical school plans to use to determine the prevalence of the virus in Houston. Similar testing has been conducted in other cities. Who is Baylor Medicine testing for COVID-19? This is a blood test to detect whether a person has been infected with this virus by measuring the antibody response in blood. LOCKED INSIDE: An outbreak at the county jail was a nightmare scenario — then it happened. Critics called the field “the wild, wild West.”, “There’s been lots of anecdotal evidence of false positives and false negatives,” said Catherine Troisi, a professor of epidemiology and infectious disease at the UTHealth School of Public Health. Even the best are flawed, it found. Fiber cell hollow-fiber bioreactor production (100 - 1000 mg) Request Quote. Request Quote. Receive treatment for a variety of symptoms including cough, nausea, fever and COVID-19, all from the comfort of your own home. From there, Baylor can hone in on the areas where infection rates are highest. Connect with friends faster than ever with the new Facebook app. Baylor College of Medicine is recruiting participants for a study to determine COVID-19’s prevalence in Greater Houston, the medical research hospital announced in a news release Oct. 21. Hybridoma cell culture (per liter) (recommended scale: 2-liter) $ 345. But most were unreliable, it turned out. It is now separating the two. Find the communities where the virus has been more prevalent and that’s where to focus public health resources.”, Like us on Facebook to see similar stories, Flint water crisis: Many residents say they still don't trust tap water, Scottish seafood sector warns Brexit risking its future. Dr. Pedro Piedra with Baylor College of Medicine explained antibody tests will look to see if someone has already been infected, indicating their body fought off the virus successfully. An outbreak at the county jail was a nightmare scenario — then it happened, envisions a study testing the blood of about 5,000 people reflective of the area’s. “The challenge is to not to mistake previous coronavirus infections — common, milder — for the new coronavirus.”. 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. It followed a report by more than 50 scientists that found just three of every 14 coronavirus antibody tests provide consistently reliable results. Shah and others said they aren’t sure to what extent unvalidated antibody tests are proliferating in the Houston area, hearing occasional anecdotal reports but little beyond that. 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 … Though most experts believe it would be unusual if antibodies to the coronavirus didn’t confer protection for some significant period of time, researchers are scrambling to study how long and what levels they must reach for optimal protection. “No one really knows if most of them work.”, Troisi notes that just 13 of the roughly 200 tests have been vetted by the Food and Drug Administration and says, “Right there, you see there might be a problem.”. This partnership is currently conducting a placebo-controlled trial that will test the safety and effectiveness of the anti-viral drug Remdesivir. meaning it produced false negatives 10 percent of the time. As COVID-19 cases continue to surge, people are wondering about antibodies and immunity. Match Day pairs fourth-year medical students with residency programs across the country for their next three to six years of training. 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. 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. Microsoft may earn an Affiliate Commission if you purchase something through recommended links in this article. Here’s the problem. This website provides Baylor University students, faculty, staff, parents and visitors with the latest information from the Centers for Disease Control and Prevention (CDC), Texas Department of State Health Services (DSHS) and Waco-McLennan County Public Health District about the evolving Novel (new) Coronavirus (COVID-19) global outbreak. RELATED: Coronavirus antibody tests have proliferated in San Antonio. Here’s the problem. Baylor College of Medicine researchers last week presented evidence to school leadership that the blood test it developed to detect whether an individual has been infected with the coronavirus … That’s better than the 90/90 standard White House coronavirus task force coordinator Dr. Deborah Birx has set for manufacturers. Antibody testing will help determine the extent of community spread. In partnership with the Centers for Disease Control and Prevention (CDC), Rice University and Baylor College of Medicine, the health department is launching a new COVID-19 antibody … CPT coding is the sole responsibility of the billing party. Baylor College of Medicine is committed to vaccinating our patients as quickly as we can. MLB antibody study: 0.7% of those tested had been exposed to coronavirus. 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. Baylor College of Medicine president, CEO and executive dean Dr. Paul Klotman speaks during Match Day Friday, March 16, 2018 in Houston. “Everything you hear is that the virus is ravaging communities of color, people at high risk,” said Klotman. 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. About 200 companies have manufactured tests, easily more than for any other disease. Baylor College of Medicine to better understand #COVID19 and stop its spread. But Klotman said such individual use of its test is “well down the road” as it prioritizes community testing for public health planning. 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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