Daniel Kling
- Scientist; PhD
Publications 2024
A mathematical framework for genetic relatedness analysis involving X chromosome aneuploidies
Forensic Sci Int Genet, 74, 103128 (in press)
DOI 10.1016/j.fsigen.2024.103128, PubMed 39243525
The power of hybridization capture - Illustrated using an expanded gene panel on 100 post mortem samples, focusing on sudden unexplained death
Forensic Sci Int Genet, 74, 103160 (in press)
DOI 10.1016/j.fsigen.2024.103160, PubMed 39437498
FamLink2 - A comprehensive tool for likelihood computations in pedigrees analyses involving linked DNA markers accounting for genotype uncertainties
Forensic Sci Int Genet, 74, 103150 (in press)
DOI 10.1016/j.fsigen.2024.103150, PubMed 39395302
Publications 2023
Single-cell transcriptome sequencing allows genetic separation, characterization and identification of individuals in multi-person biological mixtures
Commun Biol, 6 (1), 201
DOI 10.1038/s42003-023-04557-z, PubMed 36805025
Improved computations for relationship inference using low-coverage sequencing data
BMC Bioinformatics, 24 (1), 90
DOI 10.1186/s12859-023-05217-z, PubMed 36894920
Publications 2022
Whole exome sequencing of FFPE samples-expanding the horizon of forensic molecular autopsies
Int J Legal Med, 137 (4), 1215-1234
DOI 10.1007/s00414-022-02906-x, PubMed 36346469
Extended population genetic analysis of 12 X-STRs - Exemplified using a Norwegian population sample
Forensic Sci Int Genet, 60, 102745
DOI 10.1016/j.fsigen.2022.102745, PubMed 35870434
Publications 2021
Technical in-depth comparison of two massive parallel DNA-sequencing methods for formalin-fixed paraffin-embedded tissue from victims of sudden cardiac death
Forensic Sci Int Genet, 53, 102522
DOI 10.1016/j.fsigen.2021.102522, PubMed 33945952
Impact of SNP microarray analysis of compromised DNA on kinship classification success in the context of investigative genetic genealogy
Forensic Sci Int Genet, 56, 102625
DOI 10.1016/j.fsigen.2021.102625, PubMed 34753062
Investigative genetic genealogy: Current methods, knowledge and practice
Forensic Sci Int Genet, 52, 102474
DOI 10.1016/j.fsigen.2021.102474, PubMed 33592389
Publications 2019
Forensic genealogy-A comparison of methods to infer distant relationships based on dense SNP data
Forensic Sci Int Genet, 42, 113-124
DOI 10.1016/j.fsigen.2019.06.019, PubMed 31302460
Publications 2018
On the use of dense sets of SNP markers and their potential in relationship inference
Forensic Sci Int Genet, 39, 19-31
DOI 10.1016/j.fsigen.2018.11.022, PubMed 30529859
Publications 2017
Curiosities of X chromosomal markers and haplotypes
Int J Legal Med, 132 (2), 361-371
DOI 10.1007/s00414-017-1612-8, PubMed 28547136
Evaluating the statistical power of DNA-based identification, exemplified by 'The missing grandchildren of Argentina'
Forensic Sci Int Genet, 31, 57-66
DOI 10.1016/j.fsigen.2017.08.006, PubMed 28858673
Kinship inference for males with identical Y-STR profiles using whole genome SNP data provides a deeper understanding about the level of coancestry in the Swedish male population
Forensic Sci. Int. Genet. Suppl. Ser., 6, E393-E394
DOI 10.1016/j.fsigss.2017.09.165
DNA Commission of the International Society for Forensic Genetics (ISFG): Guidelines on the use of X-STRs in kinship analysis
Forensic Sci Int Genet, 29, 269-275
DOI 10.1016/j.fsigen.2017.05.005, PubMed 28544956
Publications 2016
The successful use of familial searching in six Hungarian high profile cases by applying a new module in Familias 3
Forensic Sci Int Genet, 24, 24-32
DOI 10.1016/j.fsigen.2016.05.012, PubMed 27267559
Comments on "Kinship analysis: assessment of related vs unrelated based on defined pedigrees" by S. Turrina et al
Int J Legal Med, 130 (4), 949-951
DOI 10.1007/s00414-016-1316-5, PubMed 26797423
Publications 2015
Mixtures with relatives and linked markers
Int J Legal Med, 130 (3), 621-34
DOI 10.1007/s00414-015-1288-x, PubMed 26614310
FamLinkX - implementation of a general model for likelihood computations for X-chromosomal marker data
Forensic Sci Int Genet, 17, 1-7
DOI 10.1016/j.fsigen.2015.02.007, PubMed 25771099
Publications 2014
Toward male individualization with rapidly mutating y-chromosomal short tandem repeats
Hum Mutat, 35 (8), 1021-32
DOI 10.1002/humu.22599, PubMed 24917567
Models and implementation for relationship problems with dropout
Int J Legal Med, 129 (3), 411-23
DOI 10.1007/s00414-014-1046-5, PubMed 25108449
Population genetic analysis of 12 X-STRs in a Somali population sample
Forensic Sci Int Genet, 11, e7-8
DOI 10.1016/j.fsigen.2014.02.013, PubMed 24662329
A general model for likelihood computations of genetic marker data accounting for linkage, linkage disequilibrium, and mutations
Int J Legal Med, 129 (5), 943-54
DOI 10.1007/s00414-014-1117-7, PubMed 25425094
Familias 3 - Extensions and new functionality
Forensic Sci Int Genet, 13, 121-7
DOI 10.1016/j.fsigen.2014.07.004, PubMed 25113576
Publications 2013
Frequency data for 35 autosomal STR markers in a Norwegian, an East African, an East Asian and Middle Asian population and simulation of adequate database size
Forensic Sci. Int. Genet. Suppl. Ser., 4 (1), E378-E379
DOI 10.1016/j.fsigss.2014.01.001
Publications 2012
Using object oriented bayesian networks to model linkage, linkage disequilibrium and mutations between STR markers
PLoS One, 7 (9), e43873
DOI 10.1371/journal.pone.0043873, PubMed 22984448
FamLink--a user friendly software for linkage calculations in family genetics
Forensic Sci Int Genet, 6 (5), 616-20
DOI 10.1016/j.fsigen.2012.01.012, PubMed 22390853
Analysis of Investigator HDplex markers in Swedish and Somali populations
Forensic Sci Int Genet, 7 (1), e21-2
DOI 10.1016/j.fsigen.2012.08.006, PubMed 22921958
Publications 2011
DNA microarray as a tool in establishing genetic relatedness--Current status and future prospects
Forensic Sci Int Genet, 6 (3), 322-9
DOI 10.1016/j.fsigen.2011.07.007, PubMed 21813350