Best Pathology Lab in India for Blood Test & Full Body Checkup Test Slash Sanger Confirmation Single Variant in Ahmedabad

Sanger Confirmation Single Variant in Ahmedabad

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Sanger Confirmation Single Variant
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FAQ

Can deletions be found using Sanger sequencing?

Sanger sequencing is a reliable diagnostic method that can identify the presence of a point mutation or minor deletion/duplication.

How long will the results take?

The reports would take 24-48 hours.

Why should I book Sanger Confirmation Single Variant Test with Sterling Accuris Diagnostics?

Sterling Accuris Diagnostics is at the forefront of pathology services in India, with international quality standards. Our NABL-accredited laboratory specializes in providing quick and reliable primary diagnosis support for hospitals, physicians and other healthcare facilities across the country. 

It is extremely convenient to book a Sanger Confirmation Single Variant Test with us that would give you accurate and precise results at a great price.

What makes Sterling Accuris a better pathology lab than others?

For us, precision care, safe sample collection, timely delivery of reports, and precise reporting of patient results while adhering to health and safety precautions are the cornerstone of our success.

What other packages does Sterling Accuris offer?

Sterling Accuris offers a range of packages including Senior citizen (male and female) package, healthy heart profile, diabetes profile, vitamin profile, covid immunity package and much more. Visit our website to learn more about these packages.

Do you provide home visit/collection service?

Yes. We do provide home collection services at your doorstep.

Please go ahead and book your visit today from our top menu options in this website / chat or do call us on 812 813 0000.

Is there any preparation or precautions for patient before tests or body checkup?

Fasting maybe required in case of a few tests to ensure accurate results. 

In general, it is also advisable to abstain from alcohol and heavy diet at least for 24 hours before any health test. You can see the requirement for each test on the product page on our website / app.

How long does it take to receive test results?

Though most tests are completed and reported within about 24 hours of receiving the sample for testing, certain tests take several days to weeks.

Your soft copy will be sent on registered email id and Whatsapp. Also, you will receive SMS with link to download your report. Also, your report is available on our website / app.

To know the status of the report, you can call our customer care team on 812 813 0000.

Sanger Confirmation Single Variant Test in Ahmedabad

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Sterling Accuris Diagnostics offers the Sanger Confirmation Single Variant Test in Ahmedabad for confirming the NGS variants. 

Overview of Sanger Confirmation Single Variant Test

Sanger sequencing is a quick and economical approach to read the sequence of small, targeted genomic sections. It is frequently used to check for known familial variations, to validate NGS results, and, in rare cases, for single gene sequencing. When testing is done utilising NGS technology for the proband and all other family members, this test confirms the reported variations. All of the significant SNPs, hotspots, and rare variants in the human genome can also be sequenced using the Sanger method. You can use this test to diagnose bodily disorders and small-to-significant diseases at an early stage.

Get a Sanger Confirmation Single Variant test near you to rule out any further complications that may lead to serious diseases. For accurate and precise test results head on to Sterling Accuris Diagnostics for the Sanger Confirmation Single Variant Test in Ahmedabad

Why and when is the Sanger Confirmation Single Variant Test done?

Doctors recommend this test as the most precise method of DNA sequencing. The following uses are still widespread in clinical laboratories:

  • A single gene's diagnostic sequence
  • Looking for a particular familial sequencing variation Prenatal testing for known familial variants
  • Predictive genetic testing in at-risk relatives (for example, for a familial BRCA1 variant conferring breast cancer risk)
  • Carrier testing for parents when a child has an autosomal recessive disorder (for example, cystic fibrosis)
  • Segregation analysis to assist in the interpretation of the pathogenicity of a variant (for example, by determining whether a variant under investigation is proband).
  • To verify the variations discovered by next-generation sequencing (NGS).
  • To fill any gaps in NGS data.

Sanger Confirmation Single Variant Test: Main Highlights

  • Instructions: Avoid eating or drinking for 10–12 hours before the test.
  • Recommended Age: Any age group
  • Sample type for test: Blood, Amniotic fluid, chorionic villi, and fetal tissue (POC).

Understanding how to interpret Sanger Confirmation Single Variant Test Reports 

Sanger sequencing generates a four-color chromatogram that shows the peak fluorescence intensity connected to each labelled ddNTP along the DNA sequence. A sequence text file is also frequently created by automated analysis. But for precise sequence analysis and to correct any potential errors brought about by automated base calling, a chromatogram inspection is necessary.

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Benefits of Packages with us

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Lab test Booked

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50,00,000+

Satisfied Customers

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250+

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Cities we are present
50+

Cities we are present in

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