BIO-GENETICS LABORATORY
NPI 1164523478
Clinical Medical Laboratory in St Petersburg, 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.

Gene analysis ((platelet-derived growth factor receptor, alpha polypeptide) targeted sequence

Gene analysis for the platelet-derived growth factor receptor, alpha polypeptide (PDGFRA) involves sequencing this specific gene. The test can identify genetic changes or mutations that may cause certain health conditions. It's a non-invasive procedure that helps in early detection and personalized treatment plans.

This service was performed 1,432 times for 1,432 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 2,317 times for 2,317 patients

Gene analysis (adenomatous polyposis coli), full gene sequence

Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.

This service was performed 1,399 times for 1,399 patients

Gene analysis (bloom syndrome, recq helicase-like)

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

This service was performed 1,866 times for 1,866 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

This service was performed 575 times for 575 patients

Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence

Gene analysis of the CCAAT/Enhancer Binding Protein (C/EBP), Alpha, involves studying the entire sequence of this particular gene. This can help identify variations or changes in the gene that might affect your health. This process is done in a lab using a sample of your cells.

This service was performed 1,432 times for 1,432 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 2,242 times for 2,242 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 2,777 times for 2,777 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 450 times for 450 patients

Gene analysis (cytochrome p450 family 3 subfamily a member 5) for common variant

Gene analysis for the cytochrome P450 3A5 variant helps understand your body's response to certain medications. It's a genetic test that examines how your body metabolizes drugs, aiding in personalized medication plans.

This service was performed 21 times for 21 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 1,414 times for 1,414 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 2,132 times for 2,132 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 2,293 times for 2,293 patients

Gene analysis (dihydropyrimidine dehydrogenase) for common variant

Gene analysis for dihydropyrimidine dehydrogenase (DPD) common variant involves studying a specific gene in your body. This gene affects how your body processes certain medications. The test identifies any changes in this gene which may influence your response to these medications.

This service was performed 21 times for 21 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 448 times for 448 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 451 times for 451 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 450 times for 450 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 465 times for 465 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 465 times for 465 patients

Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis

Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.

This service was performed 261 times for 261 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis

Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.

This service was performed 258 times for 258 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

This service was performed 267 times for 267 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant

Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.

This service was performed 465 times for 465 patients

Gene analysis (nudix hydrolase 15) for common variants

Gene analysis for Nudix Hydrolase 15 common variants is a genetic test that identifies changes in your NUDT15 gene. These changes can affect how your body responds to certain medications, helping your healthcare provider to personalize your treatment plan.

This service was performed 812 times for 812 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 1,842 times for 1,842 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 1,859 times for 1,859 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 465 times for 465 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

This service was performed 258 times for 258 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 2,339 times for 2,339 patients

Gene analysis (runt related transcription factor 1) targeted sequence analysis

Gene analysis for RUNX1 involves studying a specific part of your DNA. This test helps identify changes or mutations in the RUNX1 gene, which can provide insights into certain health conditions. It's like reading a book to find any spelling mistakes that could change the story.

This service was performed 1,897 times for 1,897 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 2,137 times for 2,137 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 1,880 times for 1,880 patients

Gene analysis (thiopurine s-methyltransferase) for common variant

Gene analysis for thiopurine S-methyltransferase (TPMT) involves studying your DNA to predict how your body might respond to certain medications. It helps in personalizing your treatment plan, reducing the risk of adverse effects.

This service was performed 809 times for 809 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 1,432 times for 1,432 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence

Gene analysis of v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog (KIT) is a test that studies a specific gene associated with cell growth and development. It helps in identifying any alterations in this gene that may lead to health issues.

This service was performed 1,432 times for 1,432 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 465 times for 465 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

10D1002586

Facility Type

Independent

Certificate Effective Date

December 15, 2025

Certificate Expiration Date

December 14, 2027

Laboratory Director

DR. ELI J. PIATIGORSKY

Certificate Type

Certificate of Accreditation

Certificate Type Description

This is a CLIA certificate is issued to Bio-genetics Laboratory 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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