ELITE BIO REFERENCE LABORATORY LLC
NPI 1275292294
Clinical Medical Laboratory in Tampa, FL

Areas of Expertise

The following services and procedures, recently provided to Medicare patients, illustrate the range of care this provider offers. This list reflects the variety of services available to all patients visiting the practice and is based on 2022 Medicare dataset. In general, the more frequently a provider treats specific conditions or performs particular procedures, the more experienced they become in addressing similar patient needs. The provider has delivered many of the services listed below to Medicare patients. Please note that this list does not include services provided to patients who are not covered by Medicare.

2019-ncov coronavirus, sars-cov-2/2019-ncov (covid-19), any technique, multiple types or subtypes (includes all targets), non-cdc

This refers to a test for COVID-19, caused by the SARS-CoV-2 virus. The test identifies multiple types or subtypes of the virus, including all targets. It's not specifically based on the CDC's testing protocol. It helps determine if you're currently infected with the virus.

This service was performed 235 times for 213 patients

Detection test by nucleic acid for chlamydia pneumoniae, amplified probe technique

This test checks for the presence of Chlamydia pneumoniae, a bacterium that can cause respiratory infections. It uses an amplified probe technique, which magnifies the bacterium's genetic material for easier detection. It's a standard, non-invasive procedure.

This service was performed 1,029 times for 757 patients

Detection test by nucleic acid for chlamydia trachomatis, amplified probe technique

A detection test by nucleic acid for chlamydia trachomatis, amplified probe technique, is a test that identifies the presence of a specific bacteria in the body. This bacteria can cause various health issues. The technique amplifies the sample to improve accuracy.

This service was performed 28 times for 27 patients

Detection test by nucleic acid for cytomegalovirus (cmv), amplified probe technique

A detection test by nucleic acid for cytomegalovirus (CMV) using an amplified probe technique is a lab procedure. It identifies the presence of CMV, a common virus, in your body. This technique amplifies the virus's genetic material, making it easier to detect.

This service was performed 868 times for 641 patients

Detection test by nucleic acid for enterovirus (intestinal virus), amplified probe technique

This test identifies the presence of an enterovirus, a type of virus that primarily targets the digestive system. It uses a method called the amplified probe technique to boost the detection of the virus's genetic material, or nucleic acid.

This service was performed 1,039 times for 767 patients

Detection test by nucleic acid for herpes virus-6, amplified probe technique

A detection test by nucleic acid for herpes virus-6, amplified probe technique, is a lab procedure that identifies the presence of herpes virus-6 in your body. It does this by amplifying and detecting the virus's genetic material, aiding in accurate diagnosis and treatment planning.

This service was performed 868 times for 641 patients

Detection test by nucleic acid for legionella pneumophila (water borne bacteria), amplified probe technique

A detection test for Legionella Pneumophila, a waterborne bacteria, uses the amplified probe technique. This involves identifying the bacteria's unique genetic material (nucleic acid) and amplifying it for easier detection, aiding in accurate diagnosis.

This service was performed 1,029 times for 757 patients

Detection test by nucleic acid for multiple types influenza virus

A detection test by nucleic acid for multiple types of influenza virus is a diagnostic procedure. It identifies the genetic material of the virus in your body. It's highly accurate and can distinguish between different flu strains, helping in prompt and precise treatment.

This service was performed 848 times for 629 patients

Detection test by nucleic acid for multiple types influenza virus, each additional influenza virus type or sub-type

This test identifies various types of influenza viruses by analyzing their genetic material, or nucleic acid. It can detect multiple flu types or sub-types, providing a more precise diagnosis to aid in appropriate treatment.

This service was performed 848 times for 629 patients

Detection test by nucleic acid for multiple types of respiratory virus, multiple types or subtypes, 3-5 targets

This test identifies different respiratory viruses by examining their nucleic acid, the building blocks of their genetic material. It can detect multiple types or subtypes, specifically 3-5 targets. This helps in diagnosing your respiratory illness accurately.

This service was performed 1,028 times for 758 patients

Detection test by nucleic acid for mycobacteria tuberculosis (tb bacteria), amplified probe technique

A detection test by nucleic acid for Mycobacteria Tuberculosis, using an amplified probe technique, is a diagnostic test for TB. It identifies the TB bacteria's genetic material in your body. It's fast, highly accurate, and can confirm TB presence even in small samples.

This service was performed 862 times for 640 patients

Detection test by nucleic acid for mycoplasma pneumoniae (bacteria), amplified probe technique

This test checks for Mycoplasma pneumoniae, a bacteria that can cause lung infection. It uses a method called amplified probe technique, which identifies the bacteria's genetic material. This helps in diagnosing the infection accurately.

This service was performed 1,029 times for 757 patients

Detection test by nucleic acid for neisseria gonorrhoeae (gonorrhoeae bacteria), amplified probe technique

This is a lab test that checks for the presence of a specific bacteria called Neisseria gonorrhoeae in your body. It uses a technique called amplified probe, which makes many copies of the bacteria's genetic material (nucleic acid) to help detect it more easily.

This service was performed 28 times for 27 patients

Detection test by nucleic acid for organism, amplified probe technique

A nucleic acid detection test is a procedure to identify specific organisms in your body. This test uses an amplified probe technique, which magnifies the genetic material of the organism, making it easier to detect. It's a precise way to diagnose infections.

This service was performed 11,743 times for 840 patients

Detection test by nucleic acid for respiratory syncytial virus, amplified probe technique

This test identifies the presence of the Respiratory Syncytial Virus (RSV) in your body. It uses a technique called the amplified probe, which increases the amount of viral genetic material, making it easier to detect. This helps in diagnosing RSV infections accurately.

This service was performed 1,042 times for 772 patients

Detection test by nucleic acid for staphylococcus aureus (bacteria), amplified probe technique

A detection test for Staphylococcus aureus uses a method called the amplified probe technique. This method identifies the bacteria's unique genetic material, or nucleic acid, helping to confirm its presence. It's a highly accurate way to detect this type of bacteria.

This service was performed 982 times for 745 patients

Detection test by nucleic acid for staphylococcus aureus, methicillin resistant (mrsa bacteria), amplified probe technique

A detection test by nucleic acid for MRSA bacteria uses an amplified probe technique. It's a lab procedure that identifies the presence of MRSA, a type of bacteria resistant to many antibiotics. This test helps in deciding the best treatment.

This service was performed 136 times for 124 patients

Detection test by nucleic acid for strep (streptococcus, group a), amplified probe technique

This test detects Group A Streptococcus bacteria in your body. It uses an amplified probe technique, which amplifies the bacteria's nucleic acid, making it easier to identify. This test helps diagnose conditions like strep throat or scarlet fever.

This service was performed 1,119 times for 845 patients

Detection test by nucleic acid for strep (streptococcus, group b), amplified probe technique

A detection test by nucleic acid for Group B Strep uses an amplified probe technique. This test identifies the presence of Group B Strep bacteria in the body. It involves collecting a sample, usually a swab, which is then examined in a lab for the bacteria's genetic material.

This service was performed 1,037 times for 800 patients

Detection test by nucleic acid for trichomonas vaginalis (genital parasite), amplified probe technique

This is a test to identify a common microscopic organism that can cause discomfort. The technique involves using a special probe to amplify the organism's genetic material, making it easier to detect. It's a simple, safe, and accurate procedure.

This service was performed 30 times for 29 patients

Detection test by nucleic acid for vancomycin resistance strep (vre), amplified probe technique

The detection test by nucleic acid for vancomycin-resistant strep (VRE) is a laboratory procedure. It uses an amplified probe technique to identify specific genetic material in bacteria. This helps determine if the bacteria are resistant to the antibiotic vancomycin.

This service was performed 355 times for 315 patients

Detection test for candida species (yeast), amplified probe technique

This test helps identify Candida, a type of fungus often present in the human body. An amplified probe technique is used, which enhances detection of the fungus in a sample. This method increases the accuracy of the test, helping to determine the best treatment.

This service was performed 1,111 times for 683 patients

Detection test for gardnerella vaginalis (bacteria), amplified probe technique

This test helps find a specific type of bacteria in the body. It uses a method called the amplified probe technique, which amplifies the bacteria's genetic material, making it easier to detect. It's a standard, pain-free procedure.

This service was performed 17 times for 16 patients

Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms

A definitive drug test identifies specific drugs in your system. It uses advanced methods like gc/ms and lc/ms, which can distinguish between different types of drugs but not necessarily their 3D forms. This test offers detailed results to support your healthcare decisions.

This service was performed 525 times for 354 patients

Fetal congenital abnormalities, biochemical assays of two proteins (papp-a, hcg [any form]), utilizing maternal serum, algorithm reported as a risk score

This test examines two proteins in a mother's blood to detect potential irregularities in the unborn baby's development. The results, combined with other factors, provide a risk score that helps assess the likelihood of certain conditions.

This service was performed 31 times for 31 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants

Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.

This service was performed 459 times for 459 patients

Gene analysis (additional sex combs like 1, transcriptional regulator) full sequence analysis

Gene analysis, specifically of the Additional Sex Combs Like 1, is a process where your DNA is examined to identify changes or alterations in a particular gene. This analysis helps to understand certain health conditions better and can guide treatment decisions.

This service was performed 332 times for 332 patients

Gene analysis (aspartoacylase)

Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.

This service was performed 331 times for 331 patients

Gene analysis (ataxin 7) for abnormal alleles

Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.

This service was performed 30 times for 30 patients

Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence

Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.

This service was performed 387 times for 387 patients

Gene analysis (coagulation factor ix) full sequence analysis

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

This service was performed 353 times for 353 patients

Gene analysis (coagulation factor v) leiden variant

Gene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.

This service was performed 269 times for 269 patients

Gene analysis (cystatin b) of full sequence

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

This service was performed 386 times for 386 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

This service was performed 350 times for 350 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants

Gene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.

This service was performed 56 times for 56 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants

Gene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.

This service was performed 28 times for 28 patients

Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants

Gene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.

This service was performed 123 times for 123 patients

Gene analysis (enhancer of zeste 2 polycomb repressive complex 2 subunit) of full sequence

Gene analysis of the full sequence of the Enhancer of Zeste 2 Polycomb Repressive Complex 2 Subunit (EZH2) involves examining this specific gene in detail. This gene plays a crucial role in cell growth and division. The analysis helps identify any mutations that could potentially lead to health issues.

This service was performed 332 times for 332 patients

Gene analysis (fanconi anemia, complementation group c) common variant

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

This service was performed 104 times for 104 patients

Gene analysis (fragile x mental retardation 2) for abnormal alleles

Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.

This service was performed 331 times for 331 patients

Gene analysis (fragile x mental retardation) abnormal alleles

Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.

This service was performed 331 times for 331 patients

Gene analysis (frataxin) of full sequence

Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.

This service was performed 547 times for 547 patients

Gene analysis (gap junction protein, beta 6, 30kda, connexin 30), common variants

Gene analysis for Connexin 30 involves studying your DNA to identify variations in the GJB6 gene. This gene helps produce a protein vital for cell communication. Detecting common variants can help understand certain health conditions.

This service was performed 30 times for 30 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

This service was performed 109 times for 109 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

This service was performed 158 times for 158 patients

Gene analysis (glucosidase, beta, acid) common variants

Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.

This service was performed 331 times for 331 patients

Gene analysis (hemochromatosis) common variants

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

This service was performed 386 times for 386 patients

Gene analysis (hexosaminidase a) common variants

Gene analysis of Hexosaminidase A common variants is a test that examines your DNA for changes in the Hex A gene. This gene is responsible for making an enzyme that breaks down certain substances in the body. Changes in this gene can lead to health issues.

This service was performed 332 times for 332 patients

Gene analysis (huntingtin) for abnormal alleles

Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.

This service was performed 331 times for 331 patients

Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants

Gene analysis for common variants in the IKBKAP gene helps understand your body's response to certain medications. This non-invasive test studies your DNA to identify variations in this gene, which can influence drug effectiveness and safety.

This service was performed 326 times for 326 patients

Gene analysis (janus kinase 2) targeted sequence analysis

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

This service was performed 110 times for 110 patients

Gene analysis (methyl cpg binding protein 2) full sequence analysis

Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.

This service was performed 644 times for 644 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

This service was performed 110 times for 110 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis

Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.

This service was performed 332 times for 332 patients

Gene analysis (neurotrophic receptor tyrosine kinase 2) translocation analysis

Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.

This service was performed 332 times for 332 patients

Gene analysis (partner and localizer of brca2) full sequence analysis

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

This service was performed 111 times for 111 patients

Gene analysis (partner and localizer of brca2) targeted sequence analysis

Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.

This service was performed 386 times for 386 patients

Gene analysis (peripheral myelin protein 22), full sequence analysis

Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.

This service was performed 330 times for 330 patients

Gene analysis (phosphatase and tensin homolog), full sequence analysis

Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.

This service was performed 429 times for 429 patients

Gene analysis (phospholipase c gamma 2) for common variants

Gene analysis for phospholipase C gamma 2 common variants is a test that checks for changes in the PLCG2 gene. These changes can sometimes lead to certain health conditions. The test uses a sample of your body's cells to analyze your DNA.

This service was performed 181 times for 179 patients

Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles

Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.

This service was performed 331 times for 331 patients

Gene analysis (prothrombin, coagulation factor ii) a variant

Gene analysis for prothrombin (also known as coagulation factor II) is a test that examines your DNA to identify any variations in the prothrombin gene. These variations could potentially affect blood clotting, leading to an increased risk of certain health conditions.

This service was performed 163 times for 163 patients

Gene analysis (retinal disorders), genomic sequence

Gene analysis for retinal disorders is a process where your DNA is examined to identify any changes or mutations that may be causing or could lead to vision problems. It's like reading a book to find any spelling mistakes that could alter the story.

This service was performed 31 times for 31 patients

Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants

Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.

This service was performed 294 times for 294 patients

Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant

Gene analysis for the solute carrier organic anion transporter family, member 1b1 (SLCO1B1), common variant, is a test that examines your DNA to identify variations in the SLCO1B1 gene. This gene plays a crucial role in the body's ability to process certain medications.

This service was performed 33 times for 33 patients

Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants

Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.

This service was performed 295 times for 295 patients

Gene analysis (survival of motor neuron 1, telomeric) for dosage/deletion

Gene analysis for survival of motor neuron 1 (SMN1) involves studying your DNA to identify changes or deletions in the SMN1 gene. This gene plays a key role in motor neuron health. Alterations can lead to conditions like spinal muscular atrophy. The process is safe and non-invasive.

This service was performed 332 times for 332 patients

Gene analysis (tata box binding protein) for abnormal alleles

Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.

This service was performed 14 times for 14 patients

Gene analysis (telomerase reverse transcriptase) targeted sequence analysis

Gene analysis of telomerase reverse transcriptase (TERT) involves studying a specific segment of your DNA. It helps understand how your body's cells age and multiply, which can be crucial in diagnosing and managing certain health conditions.

This service was performed 296 times for 296 patients

Gene analysis (transforming growth factor beta-induced) for common variants

Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.

This service was performed 89 times for 89 patients

Gene analysis (tumor protein 53) full sequence analysis

Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.

This service was performed 80 times for 79 patients

Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13

Gene analysis for v-ki-ras2 kirsten rat sarcoma viral oncogene variants in codons 12 and 13 is a test to identify specific changes in your genes. These changes could potentially indicate a higher risk for certain types of cancer.

This service was performed 62 times for 62 patients

Gene analysis for cancer (neuroblastoma)

Gene analysis for neuroblastoma is a test that studies your genes to identify abnormalities linked to this type of cancer. It helps doctors tailor treatment plans, potentially improving outcomes and reducing side effects.

This service was performed 62 times for 62 patients

Gene analysis panel for evaluation of genes associated with epilepsy

A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.

This service was performed 322 times for 322 patients

Gene analysis panel for hereditary disorders of the peripheral nervous system

A gene analysis panel for hereditary disorders of the peripheral nervous system is a test that checks for genetic mutations linked to certain nerve disorders. It helps identify if you have a higher risk of developing these conditions.

This service was performed 29 times for 29 patients

Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes

This procedure involves analyzing your genetic material to identify specific mutations that could cause severe inherited conditions. It examines 15 or more genes. The information can help in diagnosis, treatment planning, and understanding your risk for certain diseases.

This service was performed 29 times for 29 patients

Identification of organisms by genetic analysis, amplified probe technique

This procedure involves identifying organisms like bacteria or viruses in your body. It's done by amplifying a small part of their genetic material, making it easier to detect. This technique helps in accurate diagnosis and appropriate treatment.

This service was performed 81 times for 65 patients

Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, cdc or non-cdc, making use of high throughput technologies, completed within

This is a test to detect the COVID-19 virus. It uses a technique that amplifies the virus's genetic material (DNA or RNA) for detection. High throughput technologies are used for rapid and large-scale testing. The procedure is completed within a set time frame.

This service was performed 159 times for 152 patients

Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, making use of high throughput technologies as described by cms-2020-01-r

This is a test for COVID-19. It uses high-tech methods to find the virus's genetic material in your body. The amplified probe technique helps detect the virus even in small amounts. This is crucial for early detection and effective treatment.

This service was performed 159 times for 152 patients

Quantitative measurement of severe acute respiratory syndrome coronavirus 2 (covid-19] antibody

This procedure measures the level of COVID-19 antibodies in your body. It involves taking a blood sample, which is then tested in a lab. The results can indicate if you've had a past infection. However, it doesn't confirm immunity or protection against future infection.

This service was performed 872 times for 643 patients

Test for detecting genes

A gene detection test is a medical procedure that identifies specific genes in your DNA. It helps to understand your genetic makeup and potential health risks. The process involves taking a small sample of your body tissue, like blood or saliva, which is then analyzed in a lab.

This service was performed 30 times for 30 patients

Test for detecting genes associated with disease, whole mitochondrial genome

A test for the whole mitochondrial genome identifies changes in the mitochondrial DNA that may cause health issues. It involves taking a small sample of blood or tissue. The DNA is then examined for any changes linked to potential diseases.

This service was performed 30 times for 30 patients

Test for detecting genes causing hearing loss genomic sequence analysis panel, at least 60 genes

This is a genetic test that examines at least 60 different genes to identify any changes linked to hearing loss. By studying your DNA, the test can help determine if you have genes that may cause hearing loss, aiding in diagnosis and treatment planning.

This service was performed 30 times for 30 patients

Testing for presence of drug, by chemistry analyzers

Chemistry analyzers are used to detect the presence of drugs in your system. This test involves taking a small sample of your blood or urine. The sample is then analyzed for specific substances. The results help in understanding your health condition better.

This service was performed 289 times for 239 patients

CLIA Information

The Clinical Laboratory Improvement Amendments (CLIA) of 1988 applies to facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease. The CLIA Program sets standards for clinical laboratory testing and issues certificates. The NPI / CLIA crosswalk information for this NPI number is:

CLIA Number

10D2245071

Facility Type

Independent

Certificate Effective Date

May 02, 2025

Certificate Expiration Date

May 01, 2027

Laboratory Director

DR. FATEMEH R. MOUSAVI

Certificate Type

Certificate of Accreditation

Certificate Type Description

This is a CLIA certificate is issued to Elite Bio Reference Laboratory Llc on the basis of the laboratory's accreditation by an accreditation organization approved by CMS. This type of certificate is issued to a laboratories tha perform nonwaived (moderate and/or high complexity) testing.

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