The Postgraduate Institute of Medical Education and Research, Chandigarh has published a tender for "Quotation for submission of Institutional rates for Genetic Tests" on the 17 Dec 2025. This tender belongs to Genetics research services category. The vendors interested in this tender and related Genetics research services tenders can obtain further details by exploring Tendersniper web portal. Tendersniper sends regular tender alerts by email specifically addressing the user requirements (i.e., keywords, location and value range). Government business is a growing area of opportunity. The businesses are encouraged to actively monitor tender opportunities and participate in them to grow their business.
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Chandigarh has published 4 tenders in Genetics research services in the last financial year.
Out of these, 0 were published last month.
| Tender Title | Quotation for submission of Institutional rates for Genetic Tests |
|---|---|
| Tender Description | 12.Clinical exome (if variant confirmatiort by is included mention clearly)Whole exome (If variant confirmation by is included mention clearly)3.4.NGS-condition specific panelWhole genome (If variant confirmation by is included mention clearly)5Variant testing/ confirmation (per variant)6.Mitochondrial genome sequencing7Chromosomal Micro Array (aCGH) (mention resolution)8.MLPA (mention specific disorder/s if rates vary)9.Non-invasive prenatal screening10.Trisomy 21 screening by QFPCR in matemal blood11.Prenatal tests on Amniotic Fluid or CVS sample (mention cost ofeach separately) a. By (per variant)b. Maternal cell contamination testing (MCC)CFISHd. Karyotypee. CMA (315K)f. CMA (750K)g. Combination of test (any special offers)1. OF PCR + Karyotype + MCCI. FISH+ Karyotype MCCIII. QF PCR CMA (315k) + MCCiv. FISH+ CMA + MCCv. Any other offered in combination may be mentioned in remarks |
| Comments | 12.Clinical exome (if variant confirmatiort by is included mention clearly)Whole exome (If variant confirmation by is included mention clearly)3.4.NGS-condition specific panelWhole genome (If variant confirmation by is included mention clearly)5Variant testing/ confirmation (per variant)6.Mitochondrial genome sequencing7Chromosomal Micro Array (aCGH) (mention resolution)8.MLPA (mention specific disorder/s if rates vary)9.Non-invasive prenatal screening10.Trisomy 21 screening by QFPCR in matemal blood11.Prenatal tests on Amniotic Fluid or CVS sample (mention cost ofeach separately) a. By (per variant)b. Maternal cell contamination testing (MCC)CFISHd. Karyotypee. CMA (315K)f. CMA (750K)g. Combination of test (any special offers)1. OF PCR + Karyotype + MCCI. FISH+ Karyotype MCCIII. QF PCR CMA (315k) + MCCiv. FISH+ CMA + MCCv. Any other offered in combination may be mentioned in remarks |
| Published Date | |
|---|---|
| Due Date | 07 Jan 2026 00:00:00 |
| Estimated Value | 0.0 |
|---|---|
| EMD | 0 INR |
| Processing Fee | 0 INR |