scholarly journals Evaluation of ten SNP Markers for Human Identification and Paternity Analysis in Persian Population

2019 ◽  
Vol 17 (3) ◽  
pp. 68-71
Author(s):  
Sajad Habibi ◽  
Amirhossein Ahmadi ◽  
Mehrdad Behmanesh ◽  
Ali Miri ◽  
Mahmoud Tavallaie
Keyword(s):  
Human Identification ◽  
Paternity Analysis ◽  
Snp Markers

Selection of twenty-four highly informative SNP markers for human identification and paternity analysis in Koreans

2005 ◽  
Vol 148 (2-3) ◽  
pp. 107-112 ◽  
Author(s):  
Hwan Young Lee ◽  
Myung Jin Park ◽  
Ji-Eun Yoo ◽  
Ukhee Chung ◽  
Gil-Ro Han ◽  
...  
Keyword(s):  
Human Identification ◽  
Paternity Analysis ◽  
Snp Markers ◽  
Selection Of

Selection and use of SNP markers for animal identification and paternity analysis in U.S. beef cattle

2002 ◽  
Vol 13 (5) ◽  
pp. 272-281 ◽  
Author(s):  
Michael P. Heaton ◽  
Gregory P. Harhay ◽  
Gary L. Bennett ◽  
Roger T. Stone ◽  
W. Michael Grosse ◽  
...  
Keyword(s):  
Beef Cattle ◽  
Paternity Analysis ◽  
Snp Markers ◽  
Animal Identification

Revealing the genetic diversity of wheat varieties (lines) in China based on SNP markers

2019 ◽  
Vol 46 (2) ◽  
pp. 307-314
Author(s):  
Yu-Qing ZHANG ◽  
Juan ZOU ◽  
Yi-Ke LIU ◽  
Wei-Jie HE ◽  
Zhan-Wang ZHU ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Snp Markers ◽  
Wheat Varieties

An enrichment method for mapping ambiguous reads to the reference genome for NGS analysis

2019 ◽  
Vol 17 (06) ◽  
pp. 1940012
Author(s):  
Yuan Liu ◽  
Yongchao Ma ◽  
Evan Salsman ◽  
Frank A. Manthey ◽  
Elias M. Elias ◽  
...  
Keyword(s):  
Reference Genome ◽  
Association Studies ◽  
Large Fraction ◽  
Snp Markers ◽  
Alternative Methods ◽  
Probability Method ◽  
Genome Wide Association Studies ◽  
Enrichment Method ◽  
Allele Distribution ◽  
Random Method

Mapping short reads to a reference genome is an essential step in many next-generation sequencing (NGS) analyses. In plants with large genomes, a large fraction of the reads can align to multiple locations of the genome with equally good alignment scores. How to map these ambiguous reads to the genome is a challenging problem with big impacts on the downstream analysis. Traditionally, the default method is to assign an ambiguous read randomly to one of the many potential locations. In this study, we explore two alternative methods that are based on the hypothesis that the possibility of an ambiguous read being generated by a location is proportional to the total number of reads produced by that location: (1) the enrichment method that assigns an ambiguous read to the location that has produced the most reads among all the potential locations, (2) the probability method that assigns an ambiguous read to a location based on a probability proportional to the number of reads the location produces. We systematically compared the performance of the proposed methods with that of the default random method. Our results showed that the enrichment method produced better results than the default random method and the probability method in the discovery of single nucleotide polymorphisms (SNPs). Not only did it produce more SNP markers, but it also produced SNP markers with better quality, which was demonstrated using multiple mainstay genomic analyses, including genome-wide association studies (GWAS), minor allele distribution, population structure, and genomic prediction.

scholarly journals Human Identification Using Contrast Enhanced Segmented Palm-Vein Images

2020 ◽  
Vol 993 ◽  
pp. 012097
Author(s):  
K Nandini ◽  
T. Surendran ◽  
S. Sobana ◽  
B. K. Chitra ◽  
T. Kalaiselvi
Keyword(s):  
Human Identification ◽  
Contrast Enhanced ◽  
Palm Vein

Rugoscopy in human identification: a study in a sample of twins

2021 ◽  
pp. 1-9
Author(s):  
S. Braga ◽  
B. Sampaio-Maia ◽  
M. L. Pereira ◽  
I. M. Caldas
Keyword(s):  
Human Identification
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