Petr Danecek
Genetics · 2011–2021
A researcher in the Science corpus: 12 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 137 citations into it
- Molecular Biology — 96 citations into it
Whom Petr Danecek trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Sharon R. Browning
- Brian L. Browning
- Matthew Stephens
- Richard Durbin
- Markus Hsi-Yang Fritz
- Kostya Serebryany
- Po-Ru Loh
- Olivier Delaneau
Papers from Petr Danecek's perspective
Ordered by how strongly the researchers Petr Danecek trusts endorse each paper. Same corpus, a different order for every researcher.
- Exome sequencing as a tool for Mendelian disease gene discovery
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- Fast and accurate long-range phasing in a UK Biobank cohort
- The Human Gene Mutation Database: 2008 update
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Detection of sharing by descent, long-range phasing and haplotype imputation (Nature Genetics)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- A linear complexity phasing method for thousands of genomes (Nature Methods)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Twelve years of SAMtools and BCFtools (2020) — 12,495 citations
- BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data (2016) — 635 citations
- Mouse genomic variation and its effect on phenotypes and gene regulation (2011) — 1,549 citations
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- HTSlib: C library for reading/writing high-throughput sequencing data (2021) — 332 citations
- BCFtools/csq: haplotype-aware variant consequences (2016) — 408 citations
- Insights into human genetic variation and population history from 929 diverse genomes (2019) — 860 citations
- Very low-depth whole-genome sequencing in complex trait association studies (2017) — 78 citations
- Reference-based phasing using the Haplotype Reference Consortium panel (2016) — 1,643 citations
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations