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STR (short terminal repeat, nucleic acid)

Known as: STR, short terminal repeat (STR) in nucleic acid 
National Institutes of Health

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Short Tandem Repeat

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Rapid Multiplexed Genotyping of Simple Tandem Repeats using Capture and High‐Throughput Sequencing
Although simple tandem repeats (STRs) comprise ∼2% of the human genome and represent an important source of polymorphism, this… 
2010
2010
An automated instrument for human STR identification: Design, characterization, and experimental validation
The microfluidic integration of an entire DNA analysis workflow on a fully integrated miniaturized instrument is reported using… 
2009
2009
How accurate is the current picture of human genetic variation?
Our understanding of the distribution of worldwide human genomic diversity has greatly increased over recent years thanks to the… 
2007
2007
Allele frequency distribution for 21 autosomal STR loci in Bhutan.
We studied the allele frequency distribution of 21 autosomal STR loci contained in the AmpFlSTR Identifiler (Applied Biosystems… 
2006
2006
DNA sequencing and multiplex STR analysis on plastic microfluidic devices
The ability of plastic microfluidic devices with separation channel lengths of 6, 10 or 18 cm to perform high‐quality and high… 
2006
2006
TRECVID 2006 by NUS-I2R
NUS and I 2 R joint participated in the high-level feature extraction and automated search task for TRECVID 2006. In both task… 
2003
2003
Systematic study on STR profiling on blood and saliva traces after visualization of fingerprint marks.
This paper describes a systematic study of the influence of optical, physical, and chemical methods used for fingerprint… 
Review
2003
Review
2003
Interference of dye-associated fluorescence signals with quantitative analysis of chimerism by capillary electrophoresis
Interference of dye-associated fluorescence signals with quantitative analysis of chimerism by capillary electrophoresis 
2001
2001
Genotyping energy-transfer-cassette-labeled short-tandem-repeat amplicons with capillary array electrophoresis microchannel plates.
BACKGROUND Genetic analysis of microsatellite DNA is a powerful tool used in linkage analysis, gene mapping, and clinical… 
1995
1995
Somatic mutations in VNTR‐Locus D1S7 in human colorectal carcinomas are associated with microsatellite instability
To elucidate mutation mechanisms in hypervariable VNTR loci, we have studied somatic mutation events with the minisatellite probe… 
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