Genotype calling and haplotyping in parent-offspring trios.
about
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markersRare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.Construction and analysis of high-density linkage map using high-throughput sequencing dataLikelihood-based complex trait association testing for arbitrary depth sequencing data.Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.A computational method for genotype calling in family-based sequencing dataSequencing studies in human genetics: design and interpretation.Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance.Using Mendelian inheritance to improve high-throughput SNP discoveryA haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysisSequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits.Comparison of three boosting methods in parent-offspring trios for genotype imputation using simulation study.Fine-scale human genetic structure in Western France.Detecting and characterizing genomic signatures of positive selection in global populationsJoint detection of copy number variations in parent-offspring trios.GenomeLaser: fast and accurate haplotyping from pedigree genotypes.Identifying rare variants associated with complex traits via sequencing.Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.Genomic and phenotypic characterization of a wild medaka population: towards the establishment of an isogenic population genetic resource in fish.Advances in biotechnology and informatics to link variation in the genome to phenotypes in plants and animalsLinkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing.Computational analyses of ancient pathogen DNA from herbarium samples: challenges and prospects.Read-based phasing of related individuals.mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.Analysis of population-specific pharmacogenomic variants using next-generation sequencing data.Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.HAPDeNovo: a haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data.geck: trio-based comparative benchmarking of variant calls
P2860
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P2860
Genotype calling and haplotyping in parent-offspring trios.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Genotype calling and haplotyping in parent-offspring trios.
@ast
Genotype calling and haplotyping in parent-offspring trios.
@en
Genotype calling and haplotyping in parent-offspring trios.
@en-gb
type
label
Genotype calling and haplotyping in parent-offspring trios.
@ast
Genotype calling and haplotyping in parent-offspring trios.
@en
Genotype calling and haplotyping in parent-offspring trios.
@en-gb
prefLabel
Genotype calling and haplotyping in parent-offspring trios.
@ast
Genotype calling and haplotyping in parent-offspring trios.
@en
Genotype calling and haplotyping in parent-offspring trios.
@en-gb
P2093
P2860
P50
P356
P1433
P1476
Genotype calling and haplotyping in parent-offspring trios.
@en
P2093
Bingshan Li
Fabio Busonero
Hyun Min Kang
P2860
P304
P356
10.1101/GR.142455.112
P577
2012-10-11T00:00:00Z