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Utilizing genomic DNA purified from clotted blood samples for single nucleotide polymorphism genotyping.

Archives of pathology & laboratory medicine - 1 Mar 2002

Adkins Karissa K, Strom Daniel A, Jacobson Thomas E, Seemann Cara R, O'Brien Darin P, Heath Ellen M

Abstract excerpt

CONTEXT: Linking single nucleotide polymorphisms to disease etiology is expected to result in a substantial increase in the number of genetic tests available and performed at clinical laboratories. Whole blood serves as the most common DNA source for these tests. Because the number of blood samples rises with the number of genetic tests performed, alternative DNA sources will become important. One such...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Restriction Fragment Length

Share to Polymorphism, Single Nucleotide

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Source

Identifiers

PMID: 11860298
DOI: 10.5858/2002-126-0266-UGDPFC

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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