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Searched: Celiac Disease via Next Generation Sequencing HLA Typing
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Test CodeMethodPrice5271Sequencing with CNV PG-Select$990
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…typing. Over the longer term, long read sequencing will improve coverage even further and help us deal with difficult paralogous genes. WGS is a comprehensive test. It covers all diagnostic testing, cancer susceptibility testing…
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…Dr. Diane Allingham-Hawkins, Ph.D, FCCMG, FACM, the Senior Laboratory Director & Dean of Geneticists at PreventionGenetics presents "Getting More From Your Sequencing Test Copy Number Variant Detection by Next Generation Sequencing…
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Test CodeMethodPrice10453Sequencing with CNV PGxome$990186Sanger Sequencing$2490
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Test CodeMethodPrice7359Sequencing with CNV PGxome$1490
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Test CodeMethodPrice3017Sequencing with CNV PGxome$990
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Test CodeMethodPrice10149Sequencing with CNV PGxome$990
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Test CodeMethodPrice15131Sequencing with CNV PGxome$990
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Test CodeMethodPrice9911Sequencing with CNV PGxome$990916Sanger Sequencing$860
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…Dr. Diane Allingham-Hawkins explains the benefits and limitations of Copy Number Variant (CNV) detection through Next Generation Sequencing (NGS) and compares this to other methods of CNV detection like Chromosomal Microarray (CMA).…
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Test CodeMethodPrice10619Sequencing with CNV PGxome$990
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Test CodeMethodPrice15199Sequencing with CNV PG-Select$990
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…are inherited in an autosomal recessive manner and are caused by loss-of function variants in the relevant gene. Testing Strategy For this Next Generation Sequencing (NGS) test, sequencing is accomplished using exome capture probes…
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Test CodeMethodPrice10227Sequencing with CNV PGxome$990
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Test CodeMethodPrice15723Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10189Sequencing with CNV PGxome$990
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Test CodeMethodPrice12980Long Range PCR and NGS$590
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…-changing technology and growth of genetic testing. At the start of operations, PreventionGenetics had only three single gene Sanger sequencing tests on the menu. Today, a test for nearly every clinically relevant gene (~5000) via Next…
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…testing. Due to Next-Generation (NGS) sequencing technology, many whole exome based tests have gaps in coverage. Custom Panels can be enhanced to achieve complete coverage. In addition, many clinically relevant genes are present in two…
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Test CodeMethodPrice1331Sequencing with CNV PG-Select$990
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