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Endocrinology Requisition Form The University of Chicago Genetic Services Laboratories 5841 South Maryland Avenue, Room G701/MC0077, Chicago, IL 60637 Toll Free: 888.824.3637 Local: 773.834.0555 Fax:
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How to fill out next generation sequencing panels

01
Start by selecting the appropriate next generation sequencing (NGS) panel for your specific research or clinical needs.
02
Collect DNA or RNA samples from the individuals you want to sequence.
03
Prepare the samples by extracting and purifying the DNA or RNA.
04
Quantify the amount and quality of the DNA or RNA using suitable methods.
05
Prepare the library for sequencing by fragmenting the DNA or converting RNA to cDNA, followed by adapter ligation and amplification.
06
Perform quality control checks on the library to ensure it meets the required standards.
07
Sequence the libraries on a NGS platform following the manufacturer's instructions.
08
Analyze the sequencing data using bioinformatics tools to identify variants, mutations, or gene expressions.
09
Interpret the results based on the specific research or clinical question being addressed.
10
Report and analyze the findings, and integrate them into the broader context of the study or patient care.

Who needs next generation sequencing panels?

01
Researchers studying the genetic basis of diseases or traits.
02
Clinicians diagnosing or monitoring genetic disorders or cancer.
03
Biotechnology companies developing novel therapeutics or diagnostics.
04
Pharmaceutical companies conducting drug discovery and development.
05
Forensic scientists analyzing DNA evidence in criminal investigations.
06
Veterinary professionals studying genetic diseases in animals.
07
Genetic counselors providing insights into hereditary conditions.
08
Population geneticists investigating human migration patterns and evolution.
09
Conservation biologists studying genetic diversity in endangered species.
10
Agricultural scientists improving crop yield and breeding programs through genetic analysis.
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Next generation sequencing panels are a set of genetic tests that analyze multiple genes simultaneously.
Healthcare providers and laboratories carrying out genetic testing are required to file next generation sequencing panels.
Next generation sequencing panels can be filled out by entering the relevant patient information, test results, and any other required data into the designated fields.
The purpose of next generation sequencing panels is to identify genetic variations or mutations that may be linked to a particular disease or condition.
Next generation sequencing panels must report the genetic variants identified, the clinical significance of these variants, and any recommendations for further testing or treatment.
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