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James W. Schumm

Researcher at Promega

Publications -  41
Citations -  1217

James W. Schumm is an academic researcher from Promega. The author has contributed to research in topics: Multiplex & STR multiplex system. The author has an hindex of 20, co-authored 41 publications receiving 1211 citations.

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Patent

Multiplex amplification of short tandem repeat loci

TL;DR: In this paper, materials and methods for the simultaneous amplification of at least thirteen short tandem repeat loci, including specific materials and method for the analysis of thirteen such loci specifically selected by the United States Federal Bureau of Investigation as core loci for use in the Combined DNA Index System (CODIS) database.
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Development and Population Study of an Eight-Locus Short Tandem Repeat (STR) Multiplex System

TL;DR: Determination of genotypes of over 200 individuals from each of three different population/ethnic groups revealed independence of inheritance of the loci and allowed calculation of matching probability, typical paternity index, and power of exclusion for each multiplex.
Patent

Method and apparatus for DNA collection

TL;DR: A device for collection of DNA-containing materials is provided and a method of preventing DNA specimen contamination is provided which prevents extraneous DNA found in DNA evidence collection kits from interfering with DNA specimen analysis, further a device an method is provided for collecting the DNA containing material of a subject from the subject's skin this article.
Journal ArticleDOI

Multiplex sets for the amplification of polymorphic short tandem repeat loci--silver stain and fluorescence detection.

TL;DR: The multiplex PCR amplification systems offer a non-isotopic method for rapid, simple and accurate analysis of STR loci, which has immediate and valuable application in forensic analysis, paternity determination, tissue culture strain identification and bone marrow transplantation studies.
Journal ArticleDOI

General approach to analysis of polymorphic short tandem repeat loci.

TL;DR: The combination of allelic ladders and silver stain detection provides an inexpensive and general non-isotopic analytical method for DNA identification and has immediate application in forensic analysis, paternity determination, human cell line identification and monitoring of bone marrow transplants.