Anders Albrechtsen

Genetics · 2010–2018

A researcher in the Science corpus: 11 papers; trusts 31 researchers and is trusted by 16 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 151 citations into it; #1,541 of 6,854 by trust here, #850 by citations
• Molecular Biology — 104 citations into it; #3,024 of 17,773 by trust here, #3,494 by citations
• Artificial Intelligence — 21 citations into it

Whom Anders Albrechtsen trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Heng Li
2. Rasmus Nielsen
3. Nick Patterson
4. L. Skotte
5. Gonçalo R. Abecasis
6. Thorfinn Sand Korneliussen
7. Alkes L Price
8. David Reich
9. J. K. Pritchard
10. Jean-Philippe Brunet

Who trusts Anders Albrechtsen overall

1. Nicolas C. Rochette
2. Thorfinn Sand Korneliussen
3. J. Meisner
4. Katharine L Korunes
5. Mikhail Lipatov
6. Julian Catchen
7. Laurent Excoffier
8. B. Singh
9. Torsten Günther
10. Anton Nekrutenko

Papers from Anders Albrechtsen's perspective

Ordered by how strongly the researchers Anders Albrechtsen trusts endorse each paper. Same corpus, a different order for every researcher.

1. Genetic history of an archaic hominin group from Denisova Cave in Siberia (Nature)
2. Inference of population structure using multilocus genotype data. (Genetics)
3. Evaluation of next generation sequencing platforms for population targeted sequencing studies (Genome Biology)
4. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
5. Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
6. Fast model-based estimation of ancestry in unrelated individuals. (Genome Research)
7. The effects of human population structure on large genetic association studies
8. Genotype and SNP calling from next-generation sequencing data (Nature reviews genetics)
9. Improving SNP discovery by base alignment quality (Bioinform.)
10. Inferring human population size and separation history from multiple genome sequences (Nature Genetics)

Their papers

• Genotype and SNP calling from next-generation sequencing data (2011) — 1,450 citations
• Ancient human genome sequence of an extinct Palaeo-Eskimo (2010) — 818 citations
• Recalibrating Equus evolution using the genome sequence of an early Middle Pleistocene horse (2013) — 809 citations
• Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans (2013) — 859 citations
• SNP Calling, Genotype Calling, and Sample Allele Frequency Estimation from New-Generation Sequencing Data (2012) — 390 citations
• ANGSD: Analysis of Next Generation Sequencing Data (2014) — 2,718 citations
• Inferring Population Structure and Admixture Proportions in Low-Depth NGS Data (2018) — 633 citations
• Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History. (2018) — 262 citations
• A genomic history of Aboriginal Australia (2016) — 464 citations
• Estimating Individual Admixture Proportions from Next Generation Sequencing Data (2013) — 693 citations
• An Aboriginal Australian Genome Reveals Separate Human Dispersals into Asia (2011) — 746 citations