[HTML][HTML] Long-read sequencing emerging in medical genetics

T Mantere, S Kersten, A Hoischen - Frontiers in genetics, 2019 - frontiersin.org
The wide implementation of next-generation sequencing (NGS) technologies has
revolutionized the field of medical genetics. However, the short read lengths of currently …

Features and applications of haplotypes in crop breeding

JA Bhat, D Yu, A Bohra, SA Ganie… - Communications …, 2021 - nature.com
Climate change with altered pest-disease dynamics and rising abiotic stresses threatens
resource-constrained agricultural production systems worldwide. Genomics-assisted …

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

DR Nyholt - The American Journal of Human Genetics, 2004 - cell.com
In this report, we describe a simple correction for multiple testing of single-nucleotide
polymorphisms (SNPs) in linkage disequilibrium (LD) with each other, on the basis of the …

DNA pooling: a tool for large-scale association studies

P Sham, JS Bader, I Craig, M O'Donovan… - Nature Reviews …, 2002 - nature.com
DNA pooling is a practical way to reduce the cost of large-scale association studies to
identify susceptibility loci for common diseases. Pooling allows allele frequencies in groups …

Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals

DV Zaykin, PH Westfall, SS Young, MA Karnoub… - Human …, 2002 - karger.com
There have been increasing efforts to relate drug efficacy and disease predisposition with
genetic polymorphisms. We present statistical tests for association of haplotype frequencies …

Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms

T Niu, ZS Qin, X Xu, JS Liu - The American Journal of Human Genetics, 2002 - cell.com
Haplotypes have gained increasing attention in the map** of complex-disease genes,
because of the abundance of single-nucleotide polymorphisms (SNPs) and the limited …

On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles

RW Morris, NL Kaplan - Genetic Epidemiology: The Official …, 2002 - Wiley Online Library
We investigated the effect of multiple susceptibility alleles at a single disease locus on the
statistical power of a likelihood ratio test to detect association between alleles at a marker …

Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous

SL Lake, H Lyon, K Tantisira, EK Silverman, ST Weiss… - Human …, 2003 - karger.com
In the study of complex traits, the utility of linkage analysis and single marker association
tests can be limited for researchers attempting to elucidate the complex interplay between a …

Impact of complex genetic variation in COMT on human brain function

A Meyer-Lindenberg, T Nichols, JH Callicott… - Molecular …, 2006 - nature.com
Abstract Catechol-O-methyltransferase (COMT) has been shown to be critical for prefrontal
dopamine flux, prefrontal cortex-dependent cognition and activation. Several potentially …

[LIVRE][B] Statistical methods in genetic epidemiology

DC Thomas - 2004 - books.google.com
This well-organized and clearly written text has a unique focus on methods of identifying the
joint effects of genes and environment on disease patterns. It follows the natural sequence of …