Estimation of allele frequency and association mapping using next-generation sequencing data. - Su Yeon Kim; Kirk E. Lohmueller; Anders Albrechtsen; Yingrui Li; Thorfinn Korneliussen; Geng Tian; Niels Grarup; Tao Jiang; Gitte Andersen; Daniel Witte; Torben Jørgensen; Torben Hansen; et al. (BMC Bioinform., 2011)

Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data. - Thorfinn Sand Korneliussen; Ida Moltke; Anders Albrechtsen; Rasmus Nielsen (BMC Bioinform., 2013)

RelateAdmix: a software tool for estimating relatedness between admixed individuals. - Ida Moltke; Anders Albrechtsen (Bioinform., 2014)

ANGSD: Analysis of Next Generation Sequencing Data. - Thorfinn Korneliussen; Anders Albrechtsen; Rasmus Nielsen (BMC Bioinform., 2014)

Estimating IBD tracts from low coverage NGS data. - Filipe G. Vieira; Anders Albrechtsen; Rasmus Nielsen (Bioinform., 2016)

A genomic history of Aboriginal Australia. - Anna-Sapfo Malaspinas; Michael C. Westaway; Craig Muller; Vitor C. Sousa; Oscar Lao; Isabel Alves; Anders Bergström; Georgios Athanasiadis; Jade Yu Cheng; Jacob E. Crawford; Tim H. Heupink; Enrico Macholdt; et al. (Nat., 2016)

fastNGSadmix: admixture proportions and principal component analysis of a single NGS sample. - Emil Jørsboe; Kristian Hanghøj; Anders Albrechtsen (Bioinform., 2017)

A likelihood method for estimating present-day human contamination in ancient male samples using low-depth X-chromosome data. - José Víctor Moreno-Mayar; Thorfinn Sand Korneliussen; Jyoti Dalal; Gabriel Renaud; Anders Albrechtsen; Rasmus Nielsen; Anna-Sapfo Malaspinas (Bioinform., 2020)

Large-scale inference of population structure in presence of missingness using PCA. - Jonas Meisner; Siyang Liu 007; Mingxi Huang; Anders Albrechtsen (Bioinform., 2021)

Detecting selection in low-coverage high-throughput sequencing data using principal component analysis. - Jonas Meisner; Anders Albrechtsen; Kristian Hanghøj (BMC Bioinform., 2021)