PRECIPIO INC
NPI 1841375094
Clinical Medical Laboratory in New Haven, CT

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 343 times for 339 patients

Chromosome analysis for genetic defects, additional cells counted, each study

Chromosome analysis is a study that examines your body's chromosomes to identify any genetic defects. In some cases, additional cells may be counted to ensure accuracy. This can provide valuable information about potential health risks and inform treatment decisions.

This service was performed 43 times for 43 patients

Chromosome analysis for genetic defects, additional karyotypes, each study

Chromosome analysis is a test that examines the number and structure of a person's chromosomes. This is done to identify any genetic defects. Additional karyotypes, each study, are further tests that look at the arrangement of these chromosomes. This can help in detecting genetic disorders.

This service was performed 185 times for 182 patients

Chromosome analysis for genetic defects, count 15-20 cells

Chromosome analysis is a test that examines your body's cell structure to detect any genetic abnormalities. In this procedure, 15-20 cells are studied to identify any unusual changes that may indicate a genetic disorder. This helps in early detection and management of potential health issues.

This service was performed 282 times for 279 patients

Chromosome analysis for genetic defects, count 45 cells for mosaicism

Chromosome analysis is a test that examines your cells to identify any genetic defects. In this procedure, 45 cells are studied to check for mosaicism, a condition where some cells have a different genetic makeup. This can provide valuable information about your health and potential genetic disorders.

This service was performed 31 times for 31 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 1,026 times for 951 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 27,469 times for 879 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 956 times for 880 patients

Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase)

Gene analysis of the ABL1 gene helps identify changes that may cause certain health issues. It involves examining the ABL1 gene, which makes a protein involved in cell division and communication. This test aids in diagnosing and managing treatment for these conditions.

This service was performed 43 times for 20 patients

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

Gene analysis, specifically for the additional sex combs like 1, transcriptional regulator, is a targeted sequence analysis. This test examines specific regions of a gene to identify any changes or mutations. These changes can help understand certain health conditions and guide future health decisions.

This service was performed 106 times for 105 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 213 times for 209 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 19 times for 18 patients

Gene analysis (fms-related tyrosine kinase 3) internal tandem duplication variants

Gene analysis for FLT3 internal tandem duplication variants is a process that examines your DNA to identify specific genetic changes. These changes might influence the development of certain conditions, like leukemia. The analysis aids in determining the most effective treatment plan.

This service was performed 19 times for 18 patients

Gene analysis (isocitrate dehydrogenase 1 [nadp+], soluble) for common variants

Gene analysis for common variants of Isocitrate Dehydrogenase 1 (IDH1) is a procedure to identify changes in this specific gene. These changes can help predict certain health conditions and aid in personalized treatment planning.

This service was performed 19 times for 18 patients

Gene analysis (isocitrate dehydrogenase 2 [nadp+], mitochondrial) for common variants

Gene analysis for isocitrate dehydrogenase 2 (IDH2), a mitochondrial enzyme, helps detect common genetic variants. This procedure aids in understanding your genetic makeup, which can influence health and disease risk. It's performed using a simple blood sample.

This service was performed 19 times for 18 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 213 times for 209 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 222 times for 217 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 211 times for 207 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 36 times for 36 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 19 times for 18 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 105 times for 104 patients

Gene analysis (splicing factor [3b] subunit b1) for detection of common variants

Gene analysis for splicing factor 3b subunit b1 detects common variants. It's a test that examines your DNA, specifically the SF3B1 gene, to identify any changes or mutations. These variations can sometimes be linked to certain health conditions.

This service was performed 136 times for 135 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 18 times for 17 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 43 times for 43 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 83 times for 46 patients

Genetic sequencing localization, each multiplex procedure

Genetic sequencing localization, each multiplex procedure, is a method used to identify specific areas in your DNA. It involves studying multiple genes at once to detect variations or mutations that might be linked to certain health conditions. This process helps in understanding your genetic makeup and potential health risks.

This service was performed 148 times for 74 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 85 times for 47 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 340 times for 336 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 2,122 times for 586 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 1,151 times for 413 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 501 times for 490 patients

Molecular pathology procedure; physician interpretation and report

A molecular pathology procedure involves analyzing your body's cells at a molecular level to identify any abnormalities. This can help detect diseases early. A physician will interpret the results and provide a detailed report, explaining the findings clearly.

This service was performed 565 times for 467 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 575 times for 317 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 291 times for 285 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 2,320 times for 316 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 1,463 times for 245 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 502 times for 278 patients

Test for detecting genes associated with blood cancer

This test identifies specific genes linked to blood cancer. It involves taking a blood sample, which is then analyzed in a lab. Changes in your genes can indicate a higher risk of developing blood cancer. Understanding these risks can aid in early detection and treatment planning.

This service was performed 19 times for 18 patients

Test for detecting genes associated with blood related cancer

This test examines your DNA to identify any genetic changes that could indicate a risk for blood-related cancers. It's a simple process where a sample of your blood or saliva is taken and sent to a lab for detailed examination.

This service was performed 12 times for 12 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 321 times for 317 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 105 times for 64 patients

Translocation analysis (bcr/abl1) minor breakpoint

Translocation analysis (bcr/abl1) minor breakpoint is a genetic test that identifies specific changes in chromosomes. It's used to diagnose certain types of blood cancers. The test detects rearrangements of genetic material, aiding in the treatment plan.

This service was performed 71 times for 50 patients

Translocation analysis (bcr/abl1) other breakpoint

Translocation analysis (bcr/abl1) is a genetic test that detects abnormal chromosome changes in your body's cells. This specific test identifies a unique breakpoint in the bcr/abl1 genes, often associated with certain types of blood disorders.

This service was performed 71 times for 50 patients

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