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Genetic Testing: Difference between revisions
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==Genomic Sequencing History== | |||
The trajectory from first generation sequencing (Sanger), to Next Generation Sequencing (NGS) to whole exome to whole genome. | |||
[[File:Genomic sequencing history.jpg|600px]] | |||
==Resources== | |||
{{Members link}} | |||
[https://www.ncbi.nlm.nih.gov/books/NBK279899/#app5.Multigene_Panels Genetic Testing: Current Approaches] | |||
{{PDF|Sequence Variants - ACMG 2015.pdf}} | {{PDF|Sequence Variants - ACMG 2015.pdf}} | ||
{{PDF|Variant classification expansion - ACMG 2022.pdf}} | {{PDF|Variant classification expansion - ACMG 2022.pdf}} | ||
{{PDF|Rare disease NGS approaches - Vinksel 2020.pdf}} | |||
[[Category: | [[Category:Genetic Disorders]] |
Latest revision as of 18:15, 12 March 2023
This article is a stub.
Genomic Sequencing History
The trajectory from first generation sequencing (Sanger), to Next Generation Sequencing (NGS) to whole exome to whole genome.
Resources
Genetic Testing: Current Approaches
Sequence Variants - ACMG 2015.pdf - 349 KB (f)