A population-specific reference panel empowers genetic studies of Anabaptist populations
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A population-specific reference panel empowers genetic studies of Anabaptist populations
Authors
Keywords
-
Journal
Scientific Reports
Volume 7, Issue 1, Pages -
Publisher
Springer Nature
Online
2017-07-14
DOI
10.1038/s41598-017-05445-3
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- A reference panel of 64,976 haplotypes for genotype imputation
- (2016) NATURE GENETICS
- Unified representation of genetic variants
- (2015) Adrian Tan et al. BIOINFORMATICS
- Robust Inference of Population Structure for Ancestry Prediction and Correction of Stratification in the Presence of Relatedness
- (2015) Matthew P. Conomos et al. GENETIC EPIDEMIOLOGY
- A global reference for human genetic variation
- (2015) Richard A. Gibbs et al. NATURE
- Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
- (2015) Carlo Sidore et al. NATURE GENETICS
- Efficient haplotype matching and storage using the positional Burrows-Wheeler transform (PBWT)
- (2014) R. Durbin BIOINFORMATICS
- Using population isolates in genetic association studies
- (2014) K. Hatzikotoulas et al. Briefings in Functional Genomics
- Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
- (2014) Giorgio Pistis et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A general framework for estimating the relative pathogenicity of human genetic variants
- (2014) Martin Kircher et al. NATURE GENETICS
- Whole-genome sequence variation, population structure and demographic history of the Dutch population
- (2014) Laurent C Francioli et al. NATURE GENETICS
- Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
- (2014) Shai Carmi et al. Nature Communications
- A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness
- (2014) Jared O'Connell et al. PLoS Genetics
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
- (2014) Elaine T. Lim et al. PLoS Genetics
- Genomic View of Bipolar Disorder Revealed by Whole Genome Sequencing in a Genetic Isolate
- (2014) Benjamin Georgi et al. PLoS Genetics
- Detecting Identity by Descent and Estimating Genotype Error Rates in Sequence Data
- (2013) Brian L. Browning et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
- (2013) Qing Duan et al. BIOINFORMATICS
- Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people
- (2013) Liping Hou et al. TRENDS IN GENETICS
- Improved whole-chromosome phasing for disease and population genetic studies
- (2012) Olivier Delaneau et al. NATURE METHODS
- Kaviar: an accessible system for testing SNV novelty
- (2011) Gustavo Glusman et al. BIOINFORMATICS
- Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads
- (2011) Paolo Carnevali et al. JOURNAL OF COMPUTATIONAL BIOLOGY
- Robust relationship inference in genome-wide association studies
- (2010) Ani Manichaikul et al. BIOINFORMATICS
- Genotype imputation for genome-wide association studies
- (2010) Jonathan Marchini et al. NATURE REVIEWS GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Genetics, Medicine, and the Plain People
- (2009) Kevin A. Strauss et al. Annual Review of Genomics and Human Genetics
- Extent and distribution of linkage disequilibrium in the Old Order Amish
- (2009) Cristopher V. Van Hout et al. GENETIC EPIDEMIOLOGY
- Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
- (2009) R. Drmanac et al. SCIENCE
- Detection of sharing by descent, long-range phasing and haplotype imputation
- (2008) Augustine Kong et al. NATURE GENETICS
- Isolated populations and complex disease gene identification
- (2008) Kati Kristiansson et al. GENOME BIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More