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Publisher Correction: Analysis of transcriptomic features reveals molecular endotypes of SLE with clinical

Erika L Hubbard1,2, Prathyusha Bachali3,4, Kathryn M Kingsmore3,4

  • 1AMPEL BioSolutions, LLC, 250 W. Main St. #300, Charlottesville, VA, 22902, USA. erika.hubbard@ampelbiosolutions.com.

Genome Medicine
|December 14, 2023
PubMed
Abstract

No abstract available in PubMed .

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Comparing Copy Number Variations and SNPs02:26

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...