CYTOMETRY SPECIALISTS, INC.
NPI 1679580286
Clinical Medical Laboratory in Alpharetta, GA

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.

Bone marrow, smear interpretation

Bone marrow smear interpretation is a procedure where a small sample of your bone marrow is taken and examined under a microscope. This helps doctors identify any abnormal cells or signs of diseases such as anemia, leukemia, or infections. It's a crucial step in diagnosing various blood disorders.

This service was performed 237 times for 232 patients

Chromosome analysis for genetic defects, analyze 20-25 cells

Chromosome analysis is a test that evaluates your cells to check for genetic defects. In this procedure, 20-25 cells are examined under a microscope to identify any abnormalities. This information can help in diagnosing certain genetic conditions and guide treatment plans.

This service was performed 462 times for 436 patients

Detection test by nucleic acid for human papillomavirus (hpv), high-risk types

This test detects high-risk types of HPV, a common virus. It's done by analyzing a small sample of cells for the presence of HPV DNA. The aim is to identify any high-risk types early, as they may increase the risk of certain health issues.

This service was performed 15 times for 15 patients

Dna testing for genetic defects

DNA testing for genetic defects involves examining your DNA, the unique molecules that carry instructions for your body's functioning. The test identifies changes in chromosomes, genes, or proteins that could lead to a genetic disorder. It's a preventative measure to manage potential health risks.

This service was performed 107 times for 14 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers

Flow cytometry is a method used to measure and analyze cells. It uses a beam of light to detect up to 16 or more markers on cells, helping to identify their type, function, or abnormalities. This technique aids in diagnosing various health conditions.

This service was performed 2,185 times for 1,904 patients

Flow cytometry technique for dna or cell analysis, 2 to 8 markers

Flow cytometry is a technique that helps analyze your cells and DNA. It uses lasers to identify and sort cells based on their properties, marked by up to 8 different markers. This helps in diagnosing and monitoring various health conditions.

This service was performed 43 times for 42 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers

Flow cytometry is a technique used to measure physical and chemical characteristics of cells or particles. It can analyze multiple markers (9 to 15) on a cell, helping to identify its type and function. This process can also examine DNA within cells for any abnormalities.

This service was performed 282 times for 257 patients

Flow cytometry technique for dna or cell analysis, each additional marker

Flow cytometry is a technique that helps analyze the physical and chemical characteristics of cells or particles. When an additional marker is used, it aids in identifying specific cell types or stages of disease. This helps in precise diagnosis and treatment planning.

This service was performed 4,707 times for 180 patients

Flow cytometry technique for dna or cell analysis, first marker

Flow cytometry is a technique used to examine microscopic particles, like cells or DNA. It employs a beam of light to detect and measure physical and chemical characteristics of these particles. The 'first marker' refers to a specific characteristic or feature used to identify a particular cell or particle.

This service was performed 187 times for 183 patients

Gene analysis (calreticulin), common variants

Gene analysis of calreticulin, common variants, is a test that looks at specific genes to identify changes that may cause certain health issues. It helps in understanding your genetic makeup and potential health risks. It's a simple procedure involving a blood or saliva sample.

This service was performed 85 times for 84 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 29 times for 28 patients

Gene analysis (epidermal growth factor receptor), common variants

Gene analysis of the epidermal growth factor receptor (EGFR) identifies common variants in this particular gene. This test helps in understanding your body's response to certain medications. It aids in personalized treatment planning, ensuring the most effective care.

This service was performed 145 times for 143 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 28 times for 28 patients

Gene analysis (igh@/bcl2 (t(14;18)) translocation analysis

Gene analysis (igh@/bcl2 (t(14;18)) translocation analysis) is a specialized test that detects changes in your genes. It specifically identifies if parts of chromosomes 14 and 18 have swapped places, which can indicate certain health conditions.

This service was performed 13 times for 13 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 76 times for 73 patients

Gene analysis (janus kinase 2) variant

Gene analysis (Janus Kinase 2 variant) is a test that examines your DNA to identify any changes in the JAK2 gene. This gene is crucial for blood cell production. If it's mutated, it can lead to various blood disorders. The test helps in diagnosing these conditions.

This service was performed 171 times for 163 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants

Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.

This service was performed 88 times for 87 patients

Gene analysis (nucleophosmin) exon 12 variants

Gene analysis of nucleophosmin (exon 12 variants) is a specialized test used to identify alterations in a specific part of the NPM1 gene. These changes can help diagnose certain health conditions, particularly blood disorders. This test involves analyzing your DNA from a blood sample.

This service was performed 13 times for 12 patients

Gene analysis (t cell antigen receptor beta) amplification methodology

Gene analysis of T cell antigen receptor beta, using amplification methodology, is a process where the specific genes in your T cells are examined. This helps determine your body's immune response to diseases. It's a non-invasive procedure that aids in understanding your health better.

This service was performed 18 times for 18 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 22 times for 17 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1)

Gene analysis of v-raf murine sarcoma viral oncogene homolog b1 (BRAF) is a test that examines your DNA to identify changes or mutations in the BRAF gene. This information can help in diagnosing and treating certain diseases, including some types of cancer.

This service was performed 116 times for 116 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus) to detect abnormal clonal population amplified methodology

Gene rearrangement analysis is a test that checks for abnormal cells in your body. It focuses on a specific part of your DNA, the immunoglobulin heavy chain locus. The test amplifies this area to detect if abnormal, or 'clonal', cells are present.

This service was performed 19 times for 19 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis

Gene rearrangement analysis is a test that studies alterations in your immune system's DNA. Specifically, it evaluates the variable region somatic mutation in the immunoglobulin heavy chain locus, which helps understand your body's immune response.

This service was performed 37 times for 36 patients

Gene rearrangement analysis detection abnormal clonal population (t cell antigen receptor gamma)

Gene rearrangement analysis is a test that identifies abnormal T cells, which may indicate certain health conditions. It examines the T cell antigen receptor gamma, a key part of the immune system. It's like a detective looking for unusual patterns in your body's defenders.

This service was performed 24 times for 23 patients

Genetic sequencing localization, each additional procedure

Genetic sequencing localization is a process where specific regions of your DNA are identified and studied. If you're having additional procedures, it simply means that more areas of your DNA are being examined. This helps to understand your genetic makeup better and can assist in identifying potential health risks.

This service was performed 194 times for 165 patients

Genetic sequencing localization, initial procedure

Genetic sequencing localization is a process to identify where specific genes are located in your DNA. During the initial procedure, a sample of your cells is collected, usually through a simple swab or blood test. This data is then analyzed to pinpoint the location of certain genes. This can help understand your genetic makeup and potential health risks.

This service was performed 249 times for 232 patients

Interpretation and report of genetic testing

Interpretation and report of genetic testing involves analyzing your DNA to look for changes that could indicate a risk for certain health conditions. The results are then compiled into a report, which provides insights about your genetic health.

This service was performed 36 times for 36 patients

Microsatellite instability analysis

Microsatellite instability analysis is a test that checks for abnormalities in your DNA, which could indicate a higher risk for certain types of cancers. It is a useful tool for early detection and prevention.

This service was performed 34 times for 34 patients

Microscopic genetic analysis of tissue, computer-assisted technology, initial procedure, each multiplex procedure

This procedure involves analyzing tissue at a genetic level using a microscope and advanced computer technology. The initial process involves the collection and preparation of tissue samples. Each multiplex procedure refers to the simultaneous testing of multiple genetic markers to identify abnormalities.

This service was performed 451 times for 399 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure

Microscopic genetic analysis of tissue is a detailed lab process that examines your cells' genetic material. If more than one stain procedure is needed, it's termed an 'additional multiplex stain procedure'. This helps to highlight different components within your cells, aiding in accurate diagnosis and treatment planning.

This service was performed 4,654 times for 1,252 patients

Microscopic genetic analysis of tissue, manual, each additional procedure

Microscopic genetic analysis of tissue is a procedure where a small sample of your body tissue is examined under a microscope. This is done to study the genes in your cells. If more than one procedure is needed, each additional one involves repeating this process. It's a key part of diagnosing and managing many health conditions.

This service was performed 86 times for 72 patients

Microscopic genetic analysis of tissue, manual, initial procedure

Microscopic genetic analysis of tissue is a test that examines your cells under a microscope. This helps to identify any genetic changes that could be causing health issues. It's the first step in a series of tests to pinpoint the root cause of your symptoms.

This service was performed 703 times for 660 patients

Microscopic genetic analysis of tumor, manual

Microscopic genetic analysis of a tumor involves examining your tumor's genes under a microscope. This helps identify specific genetic changes in the tumor cells. This information can aid in diagnosing, predicting disease progression, and determining the most effective treatment options.

This service was performed 1,400 times for 934 patients

Microscopic genetic analysis of tumor, using computer-assisted technology

Microscopic genetic analysis of a tumor uses advanced computer technology to examine the genetic makeup of the tumor cells. This helps to understand the tumor better and tailor a treatment plan. It's a non-invasive procedure and provides valuable insights for your healthcare team.

This service was performed 681 times for 250 patients

Molecular pathology procedure

A molecular pathology procedure is a specialized lab test that analyzes your genes at a molecular level. It helps identify genetic variations or changes that may affect your health. This information can assist in diagnosing, monitoring, and deciding treatment for certain conditions.

This service was performed 630 times for 468 patients

Pathology examination of tissue using a microscope, intermediate complexity

A pathology examination of tissue with intermediate complexity involves studying a small sample of your body tissue under a microscope. This helps in identifying any abnormal cells or signs of disease. It's a detailed process requiring expert analysis to ensure accurate results.

This service was performed 375 times for 213 patients

Preparation of tissue for examination by removing any calcium present

This procedure involves treating tissue samples to remove any calcium, which can interfere with the examination. The tissue is soaked in a special solution that safely dissolves the calcium, leaving the tissue intact for accurate analysis. This helps in making precise diagnoses.

This service was performed 143 times for 139 patients

Special stained specimen slides to examine tissue including interpretation and report

Special stained specimen slides are used to examine tissue samples. This involves applying special dyes to the tissue, which helps to highlight certain features under a microscope. The findings are then interpreted and a report is provided. This can aid in diagnosing various health conditions.

This service was performed 1,063 times for 331 patients

Special stained specimen slides to examine tissue, each additional procedure

Special stained specimen slides are used to analyze tissue in detail. In this process, extra procedures may be needed for a more thorough examination. These involve applying special stains to the tissue on slides, enhancing specific elements for closer study.

This service was performed 4,173 times for 769 patients

Special stained specimen slides to examine tissue, each multiplex procedure

Special stained specimen slides are used to study tissue in detail. This multiplex procedure involves applying different dyes to the tissue sample on a slide to highlight specific elements. These colors help identify any abnormalities in the tissue, aiding in accurate diagnosis and treatment planning.

This service was performed 110 times for 81 patients

Special stained specimen slides to examine tissue, initial procedure

This procedure involves the use of specially stained slides to examine tissue samples. The initial process involves obtaining a small tissue sample from your body. This sample is then placed on a slide and stained with special dyes to highlight different structures and elements. The stained slide is then examined under a microscope to help diagnose any potential health issues.

This service was performed 1,142 times for 1,019 patients

Special stained specimen slides to identify organisms including interpretation and report

This service involves coloring specimen slides in a special way to help identify organisms. The colors make different parts of the organism stand out. Afterward, a detailed interpretation and report on the findings are provided.

This service was performed 98 times for 51 patients

Surgical pathology consultation and report on referred material requiring preparation of slides

A surgical pathology consultation involves the examination of tissue removed during surgery. The tissue is processed and slides are prepared for detailed study under a microscope. The findings are then compiled into a report to help guide your treatment plan.

This service was performed 259 times for 251 patients

Surgical pathology consultation and report, comprehensive

A comprehensive surgical pathology consultation and report involves the detailed examination of tissue removed during surgery. This process aids in diagnosing diseases, assessing the extent of illness, and planning appropriate treatments. The findings are then compiled into a report for your doctor.

This service was performed 142 times for 137 patients

Test for detecting genes associated with colon cancer, promoter methylation analysis

Promoter methylation analysis is a test that helps identify certain genes linked to colon cancer. This process examines how the DNA in your cells is modified, which can indicate if you're at risk for this type of cancer.

This service was performed 49 times for 49 patients

Tissue culture for tumor disorders of bone marrow and blood cells

Tissue culture for tumor disorders of bone marrow and blood cells is a lab process where your cells are grown in a controlled environment. The aim is to detect and study abnormal cells, such as cancer, in your bone marrow or blood. This helps in planning effective treatment.

This service was performed 542 times for 504 patients

Translocation analysis (bcr/abl1) major breakpoint

Translocation analysis (bcr/abl1) major breakpoint is a test that checks for a specific gene rearrangement in your cells. This rearrangement is often seen in certain types of leukemia. The test helps doctors diagnose and monitor treatment for these conditions.

This service was performed 119 times for 56 patients

Translocation analysis (pml-rara regulated adaptor molecule 1) common breakpoint

Translocation analysis (PML-RARA) is a genetic test that detects a specific change in your chromosomes, often associated with certain types of leukemia. The 'common breakpoint' refers to the exact spot where this change usually occurs. This test helps doctors diagnose and manage your condition.

This service was performed 21 times for 13 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

11D0933321

Facility Type

Independent

Certificate Effective Date

December 31, 2024

Certificate Expiration Date

December 30, 2026

Laboratory Director

DR. AMIR HAMMAMI

Certificate Type

Certificate of Accreditation

Certificate Type Description

This is a CLIA certificate is issued to Cytometry Specialists, Inc. 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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