Increasing the reference populations for the 55 AISNP panel: the need and benefits
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Bruce Budowle | Elena L. Grigorenko | Kenneth K. Kidd | Niels Morling | Haseena Rajeevan | Judith R. Kidd | Andrew J. Pakstis | Usha Soundararajan | Helle Smidt Mogensen | Sibte Hadi | K. Kidd | E. Grigorenko | J. Kidd | A. Pakstis | B. Budowle | H. S. Mogensen | N. Morling | S. Hadi | F. Wendt | L. Kang | Usha Soundararajan | T. Jin | G. E. Themudo | Haseena Rajeevan | Tianbo Jin | Longli Kang | Lijun Liu | Zhiying Zhang | Mariam Salam Al Qahtani | Lijun Liu | Zhiying Zhang | Frank R. Wendt | Goncalo E. Themudo | H. Rajeevan
[1] K. Kidd,et al. Progress toward an efficient panel of SNPs for ancestry inference. , 2014, Forensic science international. Genetics.
[2] Bruce Budowle,et al. Genetic analysis of the Yavapai Native Americans from West-Central Arizona using the Illumina MiSeq FGx™ forensic genomics system. , 2016, Forensic science international. Genetics.
[3] 52 additional reference population samples for the 55 AISNP panel. , 2015, Forensic science international. Genetics.
[4] Gabriel Silva,et al. Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America , 2009, Human mutation.
[5] P. Donnelly,et al. Inference of population structure using multilocus genotype data. , 2000, Genetics.
[6] K. Kidd,et al. Minimal SNP overlap among multiple panels of ancestry informative markers argues for more international collaboration. , 2016, Forensic science international. Genetics.
[7] Q. Kong,et al. Ancient inland human dispersals from Myanmar into interior East Asia since the Late Pleistocene , 2015, Scientific Reports.
[8] K. Kidd,et al. Genetic variation in Tunisia in the context of human diversity worldwide , 2016, American journal of physical anthropology.
[9] N. Morling,et al. Frequencies of HID-ion ampliseq ancestry panel markers among greenlanders. , 2016, Forensic science international. Genetics.
[10] Liuda Ziaugra,et al. SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform , 2009, Current protocols in human genetics.
[11] Francisco M De La Vega,et al. Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples , 2011, Investigative Genetics.
[12] Stephan J Sanders,et al. Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans , 2014, European Journal of Human Genetics.