Lista de obras - Claus Børsting - Dominio Público Uruguay

A 48-plex autosomal SNP GenPlex™ assay for human individualization and relationship testing

artículo científico publicado en 2012

A 50 SNP-multiplex mass spectrometry assay for human identification

A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing

artículo científico publicado en 2016

A mitochondrial DNA SNP multiplex assigning Caucasians into 36 haplo- and subhaplogroups

A multiplex assay with 52 single nucleotide polymorphisms for human identification

artículo científico publicado en 2006

A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes

artículo científico publicado en 2016

Analysis of 49 autosomal SNPs in an Iraqi population

artículo científico publicado en 2012

Analysis of 49 autosomal SNPs in three ethnic groups from Iran: Persians, Lurs and Kurds

scientific article published on 03 May 2013

Analysis of ancestry informative markers in three main ethnic groups from Ecuador supports a trihybrid origin of Ecuadorians

artículo científico publicado en 2017

Analysis of mainland Japanese and Okinawan Japanese populations using the precision ID Ancestry Panel

artículo científico publicado en 2017

Associations between alpha+-thalassemia and Plasmodium falciparum malarial infection in northeastern Tanzania

artículo científico publicado en 2007

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.

artículo científico publicado en 2010

Biomek 3000: the workhorse in an automated accredited forensic genetic laboratory.

artículo científico publicado en 2012

Biomek-3000 and GenPlex SNP Genotyping in Forensic Genetics

article

Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set.

artículo científico publicado en 2014

Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry

artículo científico publicado en 2007

Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing

artículo científico publicado en 2013

Comparison of manual and automated AmpliSeq™ workflows in the typing of a Somali population with the Precision ID Identity Panel

artículo científico publicado en 2017

Customizing a commercial laboratory information management system for a forensic genetic laboratory

Determination of cis/trans phase of variations in the MC1R gene with allele-specific PCR and single base extension.

artículo científico publicado en 2008

Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications.

artículo científico publicado en 2004

Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness

artículo científico publicado en 2015

Evaluation of four automated protocols for extraction of DNA from FTA cards.

artículo científico publicado en 2013

Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing

artículo científico publicado en 2014

Evaluation of the Precision ID Ancestry Panel for crime case work: A SNP typing assay developed for typing of 165 ancestral informative markers

artículo científico publicado en 2017

Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes.

artículo científico publicado en 2016

Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.

artículo científico publicado en 2013

Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans

artículo científico publicado en 2015

Forensic SNP genotyping with SNaPshot: Technical considerations for the development and optimization of multiplexed SNP assays

artículo científico publicado en 2017

Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.

artículo científico publicado en 2015

Forensic and population genetic analyses of Danes, Greenlanders and Somalis typed with the Yfiler® Plus PCR amplification kit.

artículo científico publicado en 2015

Forensic application and genetic diversity of 21 autosomal STR loci in five major population groups of Pakistan

scientific article published on 26 September 2020

Forensic genetic SNP typing of low-template DNA and highly degraded DNA from crime case samples

artículo científico publicado en 2013

Forensic typing of autosomal SNPs with a 29 SNP-multiplex--results of a collaborative EDNAP exercise.

artículo científico publicado en 2008

Forensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker set

scientific article published on 04 October 2010

Forensic validation of the SNPforID 52-plex assay

artículo científico publicado en 2007

Frequencies of 33 coding region mitochondrial SNPs in a Danish and a Turkish population

artículo científico publicado en 2010

Frequencies of HID-ion ampliseq ancestry panel markers among greenlanders.

artículo científico publicado en 2016

Genetic analyses of the human eye colours using a novel objective method for eye colour classification

artículo científico publicado en 2013

High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males

artículo científico publicado en 2005

High-throughput sequencing of core STR loci for forensic genetic investigations using the Roche Genome Sequencer FLX platform

artículo científico publicado en 2011

High-throughput sequencing of forensic genetic samples using punches of FTA cards with buccal swabs.

artículo científico publicado en 2016

Human eye colour and HERC2, OCA2 and MATP.

artículo científico publicado en 2010

ISO 17025 validation of a next-generation sequencing assay for relationship testing

artículo científico publicado en 2016

Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: Results of the 2006–2007 EDNAP collaborative exercise

artículo científico publicado en 2007

Importance of nonsynonymous OCA2 variants in human eye color prediction

artículo científico publicado en 2016

Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™.

artículo científico publicado en 2016

Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

artículo científico publicado en 2005

Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs

artículo científico publicado en 2015

Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory

artículo científico publicado en 2012

Modelling allelic drop-outs in STR sequencing data generated by MPS

scientific article published on 25 July 2018

Multiplex PCR and minisequencing of SNPs--a model with 35 Y chromosome SNPs

artículo científico publicado en 2003

Multiplex PCR with minisequencing as an effective high-throughput SNP typing method for formalin-fixed tissue

artículo científico

Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray

artículo científico publicado en 2004

Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers

scientific article published on 29 March 2010

Next generation sequencing and its applications in forensic genetics

artículo científico publicado en 2015

Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis

artículo científico publicado en 2014

Non-uniform phenotyping of D12S391 resolved by second generation sequencing.

artículo científico publicado en 2013

Peopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of Greenlanders

artículo científico publicado en 2015

Performance of the SNPforID 52 SNP-plex assay in paternity testing

artículo científico publicado en 2008

Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome

artículo científico publicado en 2016

Population and forensic data for three sets of forensic genetic markers in four ethnic groups from Iran: Persians, Lurs, Kurds and Azeris

artículo científico publicado en 2015

Quantification of massively parallel sequencing libraries - a comparative study of eight methods

artículo científico publicado en 2018

Reinvestigations of six unusual paternity cases by typing of autosomal single-nucleotide polymorphisms

artículo científico publicado en 2011

Repeated extraction of DNA from FTA cards

Results for five sets of forensic genetic markers studied in a Greek population sample

scientific article published on 05 January 2015

SNP typing of the reference materials SRM 2391b 1-10, K562, XY1, XX74, and 007 with the SNPforID multiplex.

artículo científico publicado en 2010

SNP typing on the NanoChip electronic microarray.

artículo científico publicado en 2005

Second generation sequencing of three STRs D3S1358, D12S391 and D21S11 in Danes and a new nomenclature for sequenced STR alleles

artículo científico publicado en 2014

Second-generation sequencing of forensic STRs using the Ion Torrent™ HID STR 10-plex and the Ion PGM™.

artículo científico publicado en 2014

Sequences of microvariant/“off-ladder” STR alleles

Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software.

artículo científico publicado en 2018

Sequencing of mitochondrial genomes using the Precision ID mtDNA Whole Genome Panel.

artículo científico publicado en 2018

Single Nucleotide Polymorphism

scholarly article published 15 September 2014

Skin pigmentation and genetic variants in an admixed Brazilian population of primarily European ancestry

scientific article published on 09 May 2020

The effect of gender on eye colour variation in European populations and an evaluation of the IrisPlex prediction model.

artículo científico publicado en 2014

Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator® DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey.

artículo científico publicado en 2016

Typing of 111 ancestry informative markers in an Albanian population

artículo científico publicado en 2015

Typing of 30 insertion/deletions in Danes using the first commercial indel kit—Mentype® DIPplex

artículo científico publicado en 2011

Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics

artículo científico publicado en 2008

Typing of 49 autosomal SNPs by SNaPshot® in the Slovenian population

artículo científico publicado en 2010

Typing of 49 autosomal SNPs by single base extension and capillary electrophoresis for forensic genetic testing

artículo científico publicado en 2012

Typing of Amerindian Kichwas and Mestizos from Ecuador with the SNPforID multiplex.

artículo científico publicado en 2011

Typing of Y chromosome SNPs with multiplex PCR methods.

artículo científico publicado en 2005

Understanding geographic origins and history of admixture among chimpanzees in European zoos, with implications for future breeding programmes

artículo científico publicado en 2013

Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standard.

artículo científico publicado en 2009

Vectorial acylation in Saccharomyces cerevisiae. Fat1p and fatty acyl-CoA synthetase are interacting components of a fatty acid import complex.

artículo científico publicado en 2003

What Genes Tell about Iris Appearance

artículo científico publicado en 2013

Yeast acyl-CoA-binding protein: acyl-CoA-binding affinity and effect on intracellular acyl-CoA pool size.

artículo científico publicado en 1994

Lista de obras de Claus Børsting

A 48-plex autosomal SNP GenPlex™ assay for human individualization and relationship testing

A 50 SNP-multiplex mass spectrometry assay for human identification

A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing

A mitochondrial DNA SNP multiplex assigning Caucasians into 36 haplo- and subhaplogroups

A multiplex assay with 52 single nucleotide polymorphisms for human identification

A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes

Analysis of 49 autosomal SNPs in an Iraqi population

Analysis of 49 autosomal SNPs in three ethnic groups from Iran: Persians, Lurs and Kurds

Analysis of ancestry informative markers in three main ethnic groups from Ecuador supports a trihybrid origin of Ecuadorians

Analysis of mainland Japanese and Okinawan Japanese populations using the precision ID Ancestry Panel

Associations between alpha+-thalassemia and Plasmodium falciparum malarial infection in northeastern Tanzania

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.

Biomek 3000: the workhorse in an automated accredited forensic genetic laboratory.

Biomek-3000 and GenPlex SNP Genotyping in Forensic Genetics

Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set.

Carrier frequency of a nonsense mutation in the adenosine deaminase (ADA) gene implies a high incidence of ADA-deficient severe combined immunodeficiency (SCID) in Somalia and a single, common haplotype indicates common ancestry

Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing

Comparison of manual and automated AmpliSeq™ workflows in the typing of a Somali population with the Precision ID Identity Panel

Customizing a commercial laboratory information management system for a forensic genetic laboratory

Determination of cis/trans phase of variations in the MC1R gene with allele-specific PCR and single base extension.

Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications.

Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness

Evaluation of four automated protocols for extraction of DNA from FTA cards.

Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing

Evaluation of the Precision ID Ancestry Panel for crime case work: A SNP typing assay developed for typing of 165 ancestral informative markers

Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes.

Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.

Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans

Forensic SNP genotyping with SNaPshot: Technical considerations for the development and optimization of multiplexed SNP assays

Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.

Forensic and population genetic analyses of Danes, Greenlanders and Somalis typed with the Yfiler® Plus PCR amplification kit.

Forensic application and genetic diversity of 21 autosomal STR loci in five major population groups of Pakistan

Forensic genetic SNP typing of low-template DNA and highly degraded DNA from crime case samples

Forensic typing of autosomal SNPs with a 29 SNP-multiplex--results of a collaborative EDNAP exercise.

Forensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker set

Forensic validation of the SNPforID 52-plex assay

Frequencies of 33 coding region mitochondrial SNPs in a Danish and a Turkish population

Frequencies of HID-ion ampliseq ancestry panel markers among greenlanders.

Genetic analyses of the human eye colours using a novel objective method for eye colour classification

High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males

High-throughput sequencing of core STR loci for forensic genetic investigations using the Roche Genome Sequencer FLX platform

High-throughput sequencing of forensic genetic samples using punches of FTA cards with buccal swabs.

Human eye colour and HERC2, OCA2 and MATP.

ISO 17025 validation of a next-generation sequencing assay for relationship testing

Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: Results of the 2006–2007 EDNAP collaborative exercise

Importance of nonsynonymous OCA2 variants in human eye color prediction

Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™.

Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs

Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory

Modelling allelic drop-outs in STR sequencing data generated by MPS

Multiplex PCR and minisequencing of SNPs--a model with 35 Y chromosome SNPs

Multiplex PCR with minisequencing as an effective high-throughput SNP typing method for formalin-fixed tissue

Multiplex PCR, amplicon size and hybridization efficiency on the NanoChip electronic microarray

Mutations and/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers

Next generation sequencing and its applications in forensic genetics

Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis

Non-uniform phenotyping of D12S391 resolved by second generation sequencing.

Peopling of the North Circumpolar Region – Insights from Y Chromosome STR and SNP Typing of Greenlanders

Performance of the SNPforID 52 SNP-plex assay in paternity testing

Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma Syndrome

Population and forensic data for three sets of forensic genetic markers in four ethnic groups from Iran: Persians, Lurs, Kurds and Azeris

Quantification of massively parallel sequencing libraries - a comparative study of eight methods

Reinvestigations of six unusual paternity cases by typing of autosomal single-nucleotide polymorphisms

Repeated extraction of DNA from FTA cards

Results for five sets of forensic genetic markers studied in a Greek population sample

SNP typing of the reference materials SRM 2391b 1-10, K562, XY1, XX74, and 007 with the SNPforID multiplex.

SNP typing on the NanoChip electronic microarray.

Second generation sequencing of three STRs D3S1358, D12S391 and D21S11 in Danes and a new nomenclature for sequenced STR alleles

Second-generation sequencing of forensic STRs using the Ion Torrent™ HID STR 10-plex and the Ion PGM™.

Sequences of microvariant/“off-ladder” STR alleles

Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software.

Sequencing of mitochondrial genomes using the Precision ID mtDNA Whole Genome Panel.

Single Nucleotide Polymorphism

Skin pigmentation and genetic variants in an admixed Brazilian population of primarily European ancestry

The effect of gender on eye colour variation in European populations and an evaluation of the IrisPlex prediction model.

Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator® DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey.

Typing of 111 ancestry informative markers in an Albanian population

Typing of 30 insertion/deletions in Danes using the first commercial indel kit—Mentype® DIPplex