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Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionThe Pfam protein families databaseHundreds of variants clustered in genomic loci and biological pathways affect human heightVariants in MTNR1B influence fasting glucose levels.Six new loci associated with body mass index highlight a neuronal influence on body weight regulationA census of human cancer genesGenetic Loci associated with C-reactive protein levels and risk of coronary heart diseaseGenome-wide association analysis of metabolic traits in a birth cohort from a founder populationEnhanced protein domain discovery using taxonomyTreeFam: a curated database of phylogenetic trees of animal gene familiesDetection of tuberculosis in HIV-infected and -uninfected African adults using whole blood RNA expression signatures: a case-control studyComplete Genome Sequence of Klebsiella quasipneumoniae subsp. similipneumoniae Strain ATCC 700603Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathwaysEnhanced protein domain discovery by using language modeling techniques from speech recognition.The effect of genomic inversions on estimation of population genetic parameters from SNP data.A population model for genotyping indels from next-generation sequence data.cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing datacnvCapSeq: detecting copy number variation in long-range targeted resequencing data.Pathway analysis of GWAS provides new insights into genetic susceptibility to 3 inflammatory diseases.Realtime analysis and visualization of MinION sequencing data with npReader.Small deletion variants have stable breakpoints commonly associated with alu elements.Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regionsinvertFREGENE: software for simulating inversions in population genetic data.sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors.Inferring combined CNV/SNP haplotypes from genotype dataDiagnosis of childhood tuberculosis and host RNA expression in Africa.famCNV: copy number variant association for quantitative traits in families.A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distributionMirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitizationGenetic variability in the regulation of gene expression in ten regions of the human brain.An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasisGenome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data.cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data.Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences.TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 influence different pathways leading to smoking behavior from adolescence to mid-adulthood
P50
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P50
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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Lachlan Coin
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P1053
A-9001-2014
P106
P1153
55889865800
P21
P2456
P31
P3829
P3835
lachlan-coin2
P496
0000-0002-4300-455X