402 results on '"Børsting C"'
Search Results
2. Evaluation of a custom QIAseq targeted DNA panel with 164 ancestry informative markers sequenced with the Illumina MiSeq
3. The EUROFORGEN NAME Ampliseq™ custom panel: A second tier panel developed for differentiation of individuals from the Middle East/North Africa
4. Development and validation of the EUROFORGEN NAME (North African and Middle Eastern) ancestry panel
5. Retraction notice to “Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel” [Forensic Sci. Int.: Genet. 43 (2019) 102144]
6. The Danish STR sequence database: duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit
7. Reproducibility of methylated CpG typing with the Illumina MiSeq
8. A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing
9. Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™
10. Comparison of techniques for quantification of next-generation sequencing libraries
11. Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise
12. Optimization of the collection and analysis of touch DNA traces
13. Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set
14. 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
15. Low-protein diets for broilers: Current knowledge and potential strategies to improve performance and health, and to reduce environmental impact
16. Genomic Applications in Forensic Medicine
17. List of Contributors
18. Insights into accuracy of social scientists' forecasts of societal change
19. Typing of two Middle Eastern populations with the Precision ID Ancestry Panel
20. Analysis of 16 autosomal STR loci in Uyghur and Kazakh populations from Xinjiang, China
21. Autosomal SNP typing of forensic samples with the GenPlex™ HID System: Results of a collaborative study
22. Forensic typing of autosomal SNPs with a 29 SNP-multiplex—Results of a collaborative EDNAP exercise
23. Utility of X-chromosome SNPs in relationship testing
24. Testing of the Illumina® ForenSeq™ kit
25. Typing of 111 ancestry informative markers in an Albanian population
26. Template preparation of AmpliSeq™ libraries using the Ion Chef™
27. Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel
28. Single-Nucleotide Polymorphisms
29. RETRACTED: Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel
30. Application of whole genome amplification for forensic analysis
31. Multiple displacement amplification of blood and saliva samples placed on FTA® cards
32. Genetic screening of 15 SNPs in the MC1R gene in relation to hair colour in Danes
33. Development of a multiplex PCR assay detecting 52 autosomal SNPs
34. The effect of whole genome amplification on samples originating from more than one donor
35. Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages
36. Semi-automatic preparation of biological database samples for STR typing
37. Comparison of paternity indices based on typing of 15 STRs, 7 VNTRs and 52 SNPs in 50 Danish mother–child–father trios
38. Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel
39. Drop-out probabilities of IrisPlex SNP alleles
40. Distribution of Y chromosome haplogroup Q in Greenlanders
41. Development and optimisation of five multiplex assays with 115 of the AIM SNPs from the EUROFORGEN AIMs set on the Sequenom® MassARRAY® system
42. The genetics of eye colours in an Italian population measured with an objective method for eye colour quantification
43. Assessing the potential application of X-chromosomal haploblocks in population genetics and forensic studies
44. Analysis of Uyghur and Kazakh populations using the Precision ID Ancestry Panel
45. The Danish STR sequence database:duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit
46. The EUROFORGEN NAME Ampliseq™ custom panel:A second tier panel developed for differentiation of individuals from the Middle East/North Africa
47. Analysis of 16 autosomal STR loci in Uyghur and Kazakh populations from Xinjiang, China
48. Analysis of 16 autosomal STR loci in Uyghur and Kazakh populations from Xinjiang, China
49. Implementation of the SNP forID multiplex on the Sequenom ® MassARRAY ® analyzer 4 system
50. Genetic variants and skin colour in Danes
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