What is he best known for?
The fields of study he is best known for:
John M. Butler focuses on Genetics, Microsatellite, Computational biology, Polymerase chain reaction and DNA profiling.
His Genetics and Amplicon, Multiplex, Primer, Multiplex polymerase chain reaction and Typing investigations all form part of his Genetics research activities.
John M. Butler interconnects Single-nucleotide polymorphism and Primer extension in the investigation of issues within Multiplex.
The concepts of his Microsatellite study are interwoven with issues in Genetic marker and Genotyping.
His Polymerase chain reaction research includes elements of DNA database, DNA, Mitochondrial DNA, Chromatography and Genotype.
In DNA profiling, John M. Butler works on issues like Human genome, which are connected to Genomics and Locus.
His most cited work include:
- Genetics and genomics of core short tandem repeat loci used in human identity testing. (492 citations)
- The development of reduced size STR amplicons as tools for analysis of degraded DNA. (454 citations)
- Forensic DNA typing : biology, technology, and genetics of STR markers (445 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Genetics, Microsatellite, DNA, NIST and Multiplex.
His study in Single-nucleotide polymorphism, Allele, Locus, Y-STR and Y chromosome falls within the category of Genetics.
His Microsatellite research is multidisciplinary, relying on both Typing, Computational biology, DNA profiling and Polymerase chain reaction.
His research investigates the connection between DNA and topics such as Chromatography that intersect with issues in Real-time polymerase chain reaction.
John M. Butler combines subjects such as Forensic dna and Library science with his study of NIST.
John M. Butler focuses mostly in the field of Multiplex, narrowing it down to topics relating to Primer and, in certain cases, Amplicon.
He most often published in these fields:
- Genetics (50.00%)
- Microsatellite (38.16%)
- DNA (15.79%)
What were the highlights of his more recent work (between 2013-2020)?
- Genetics (50.00%)
- Allele (10.09%)
- Microsatellite (38.16%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Genetics, Allele, Microsatellite, Forensic dna and Forensic science.
Genetics is represented through his STR multiplex system, Genotype, Locus, Allele sharing and Mitochondrial DNA research.
In his research on the topic of Allele, Polymerase chain reaction is strongly related with DNA.
John M. Butler has included themes like DNA profiling, Genotyping, Computational biology and Massive parallel sequencing, DNA sequencing in his Microsatellite study.
His DNA profiling research is multidisciplinary, incorporating perspectives in Genetic marker, Reference genome and Genomics.
Within one scientific family, John M. Butler focuses on topics pertaining to Data science under Forensic dna, and may sometimes address concerns connected to End user.
Between 2013 and 2020, his most popular works were:
- Update of the guidelines for the publication of genetic population data. (129 citations)
- Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements (128 citations)
- STR allele sequence variation: Current knowledge and future issues. (98 citations)
In his most recent research, the most cited papers focused on:
John M. Butler mostly deals with Genetics, Forensic dna, Data science, Microsatellite and Interpretation.
He incorporates Genetics and Confusion in his research.
His Forensic dna research incorporates elements of NIST and Electropherogram.
His Data science study integrates concerns from other disciplines, such as Typing and Dna evidence.
His Microsatellite research incorporates themes from dbSNP, Computational biology and Massive parallel sequencing, DNA sequencing.
His Computational biology research incorporates elements of Allele frequency, Genotype, Data curation and Mitochondrial DNA.
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