Andreas Tillmar

Dr. Andreas Tillmar

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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2014 in Forensic Science International: Genetics
Verified
Journal Article
Closed access
DKDaniel Kling
Daniel Kling
ATAndreas Tillmar
Andreas Tillmar
TEThore Egeland
Thore Egeland

10 December 2021 in Genes
Verified
Journal Article
Open access
PDF file
ATAndreas Tillmar
Andreas Tillmar
KSKimberly Sturk-Andreaggi
Kimberly Sturk-Andreaggi
JDJennifer Daniels-Higginbotham
Jennifer Daniels-Higginbotham
JTJacqueline Tyler Thomas
Jacqueline Tyler Thomas
CMCharla Marshall
Charla Marshall
The FORensic Capture Enrichment (FORCE) panel is an all-in-one SNP panel for forensic applications. This panel of 5422 markers encompasses common, forensically relevant SNPs (identity, ancestry, phenotype, X- and Y-chromosomal SNPs), a novel set of 3931 autosomal SNPs for extended kinship analysis, and no clinically relevant/disease markers. The FORCE panel was developed as a custom hybridization capture assay utilizing ~20,000 baits to target the selected SNPs. Five non-probative, previously identified World War II (WWII) cases were used to assess the kinship panel. Each case included one bone sample and associated family reference DNA samples. Additionally, seven reference quality samples, two 200-year-old bone samples, and four control DNAs were processed for kit performance and concordance assessments. SNP recovery after capture resulted in a mean of ~99% SNPs exceeding 10X coverage for reference and control samples, and 44.4% SNPs for bone samples. The WWII case results showed that the FORCE panel could predict first to fifth degree relationships with strong statistical support (likelihood ratios over 10,000 and posterior probabilities over 99.99%). To conclude, SNPs will be important for further advances in forensic DNA analysis. The FORCE panel shows promising results and demonstrates the utility of a 5000 SNP panel for forensic applications.

1 July 2017 in Forensic Science International: Genetics
Verified
Journal Article
Closed access
ATAndreas Tillmar
Andreas Tillmar
DKDaniel Kling
Daniel Kling
JBJohn M. Butler
John M. Butler
Walther ParsonWalther Parson
Walther Parson
MPMechthild Prinz
Mechthild Prinz
LGLeonor Gusmão
Leonor Gusmão

16 December 2013 in PLOS ONE
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Journal Article
Open access
PDF file
ATAndreas Tillmar
Andreas Tillmar
BDBarbara Dell'AMico
Barbara Dell'AMico
JWJenny Welander
Jenny Welander
GHGunilla Holmlund
Gunilla Holmlund
Species identification can be interesting in a wide range of areas, for example, in forensic applications, food monitoring and in archeology. The vast majority of existing DNA typing methods developed for species determination, mainly focuses on a single species source. There are, however, many instances where all species from mixed sources need to be determined, even when the species in minority constitutes less than 1 % of the sample. The introduction of next generation sequencing opens new possibilities for such challenging samples. In this study we present a universal deep sequencing method using 454 GS Junior sequencing of a target on the mitochondrial gene 16S rRNA. The method was designed through phylogenetic analyses of DNA reference sequences from more than 300 mammal species. Experiments were performed on artificial species-species mixture samples in order to verify the method’s robustness and its ability to detect all species within a mixture. The method was also tested on samples from authentic forensic casework. The results showed to be promising, discriminating over 99.9 % of mammal species and the ability to detect multiple donors within a mixture and also to detect minor components as low as 1 % of a mixed sample.

1 March 2016 in International journal of legal medicine
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Journal Article
Closed access
PDF file
IGIda Grandell
Ida Grandell
RSRaed Samara
Raed Samara
ATAndreas Tillmar
Andreas Tillmar

1 July 2021 in Forensic Science International: Genetics
Verified
Journal Article
Open access
ATAndreas Tillmar
Andreas Tillmar
SFSiri Aili Fagerholm
Siri Aili Fagerholm
JSJan Staaf
Jan Staaf
PSPeter Sjölund
Peter Sjölund
RARicky Ansell
Ricky Ansell
On the morning of October 19, 2004, an eight-year-old boy and a 56-year-old woman were stabbed to death on an open street in the city of Linköping, Sweden. The perpetrator left his DNA at the crime scene, and after 15 years of various investigation efforts, including more than 9000 interrogations and mass DNA screening of more than 6000 men, there were still no clues about the identity of the unknown murderer. The successful application of investigative genetic genealogy (IGG) in the US raised the interest for this tool within the Swedish Police Authority. After legal consultations it was decided that IGG could be applied in this double murder case as a pilot case study. From extensive DNA analysis, including whole-genome sequencing and genotype imputation, DNA data sets were established and searched within both GEDmatch and FamilyTree DNA genealogy databases. A number of fairly distant relatives were found from which family trees were created. The genealogy work resulted in two candidates, two brothers, one of whom matched the crime scene samples by routine STR profiling. The suspect confessed the murders at the initial police hearing and was later convicted of the murders. In this paper we describe the successful application of an emerging technology. We disclose details of the DNA analyses which, due to the poor quality and low quantity of the DNA, required reiterative sequencing and genotype imputation efforts. The successful application of IGG in this double murder case exemplifies its applicability not only in the US but also in Europe. The pressure is now high on the involved authorities to establish IGG as a tool for cold case criminal investigations and for missing person identifications. There is, however, a continuous need to accommodate legal, social and ethical aspects as well.