about
Using familial information for variant filtering in high-throughput sequencing studiesCombined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700sStable recombination hotspots in birdsA candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMSAncestral alleles in the human genome based on population sequencing dataA thrifty variant in CREBRF strongly influences body mass index in Samoans.Analysis of Genome-Wide Association Data.Convergent evolution of SWS2 opsin facilitates adaptive radiation of threespine stickleback into different light environments.sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors.Sequence variant at 4q25 near PITX2 associates with appendicitis.The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort.Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.Genomic islands of speciation separate cichlid ecomorphs in an East African crater lake.Whole-genome haplotyping approaches and genomic medicine.A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysisGenetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities StudyGenome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyA Genome-Wide Association Study of a Biomarker of Nicotine Metabolism.Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families.Multiple Independent Retroelement Insertions in the Promoter of a Stress Response Gene Have Variable Molecular and Functional Effects in Drosophila.Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.Evaluating the performance of selection scans to detect selective sweeps in domestic dogsComplex disease and phenotype mapping in the domestic dog.Population genomics of the filarial nematode parasite Wuchereria bancrofti from mosquitoesGenome-wide time-to-event analysis on smoking progression stages in a family-based studyGenome-wide association study of colorectal cancer in Hispanics.Fast and accurate long-range phasing in a UK Biobank cohort.Genome-wide association study of colorectal cancer identifies six new susceptibility loci.Rare variant phasing and haplotypic expression from RNA sequencing with phASERReference-based phasing using the Haplotype Reference Consortium panel.11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.A genome-wide association study yields five novel thyroid cancer risk loci.Detecting balancing selection in genomes: limits and prospects.Haplotype-resolved genome sequencing: experimental methods and applications.The Recombination Landscape in Wild House Mice Inferred Using Population Genomic Data.Securing the use of existing sample collections for future human genetic research.Genome-Wide SNP Analysis Reveals Distinct Origins of Trypanosoma evansi and Trypanosoma equiperdum.Comparative analysis of de novo assemblers for variation discovery in personal genomes.Incorporating functional annotation information in prioritizing disease associated SNPs from genome wide association studies.
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Haplotype estimation using sequencing reads.
@ast
Haplotype estimation using sequencing reads.
@en
Haplotype estimation using sequencing reads.
@nl
type
label
Haplotype estimation using sequencing reads.
@ast
Haplotype estimation using sequencing reads.
@en
Haplotype estimation using sequencing reads.
@nl
prefLabel
Haplotype estimation using sequencing reads.
@ast
Haplotype estimation using sequencing reads.
@en
Haplotype estimation using sequencing reads.
@nl
P2093
P2860
P1476
Haplotype estimation using sequencing reads.
@en
P2093
Anthony J Cox
Bryan Howie
Olivier Delaneau
P2860
P304
P356
10.1016/J.AJHG.2013.09.002
P407
P577
2013-10-01T00:00:00Z