Pages that link to "Q57087763"
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The following pages link to Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants (Q57087763):
Displaying 50 items.
- Exome sequencing identifies ZNF644 mutations in high myopia (Q21092428) (← links)
- Human genetics and genomics a decade after the release of the draft sequence of the human genome (Q21245451) (← links)
- Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice (Q24304229) (← links)
- Targeted enrichment of genomic DNA regions for next-generation sequencing (Q24618696) (← links)
- Beyond the fourth wave of genome-wide obesity association studies (Q24627723) (← links)
- Molecular basis for population variation: from SNPs to SAPs (Q27002638) (← links)
- Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed (Q27014915) (← links)
- RNA editome in rhesus macaque shaped by purifying selection (Q27316422) (← links)
- Classic selective sweeps revealed by massive sequencing in cattle (Q27316874) (← links)
- X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes (Q28118573) (← links)
- Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (Q28241532) (← links)
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study (Q28275978) (← links)
- 267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation (Q28392698) (← links)
- Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genes (Q28533822) (← links)
- Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research (Q28601377) (← links)
- Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human disease (Q28706718) (← links)
- Selective constraints determine the time dependency of molecular rates for human nuclear genomes (Q28710408) (← links)
- Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability (Q29147451) (← links)
- SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data (Q30000842) (← links)
- The contribution of rare and common variants in 30 genes to risk nicotine dependence (Q30301219) (← links)
- Patterns of coding variation in the complete exomes of three Neandertals. (Q30361631) (← links)
- Exome sequencing supports a de novo mutational paradigm for schizophrenia. (Q30405748) (← links)
- RNA-Seq approach for genetic improvement of meat quality in pig and evolutionary insight into the substrate specificity of animal carbonyl reductases (Q30421087) (← links)
- Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry (Q30437010) (← links)
- The genetic landscape of mutations in Burkitt lymphoma (Q30453771) (← links)
- Exome sequencing of senescence-accelerated mice (SAM) reveals deleterious mutations in degenerative disease-causing genes. (Q30455193) (← links)
- Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency (Q30465158) (← links)
- Large scale library generation for high throughput sequencing (Q30475485) (← links)
- Transcriptome-based exon capture enables highly cost-effective comparative genomic data collection at moderate evolutionary scales (Q30558064) (← links)
- Modeling read counts for CNV detection in exome sequencing data (Q30574430) (← links)
- A population model for genotyping indels from next-generation sequence data. (Q30580663) (← links)
- Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data (Q30584012) (← links)
- Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation (Q30661750) (← links)
- Quantifying population genetic differentiation from next-generation sequencing data (Q30663555) (← links)
- A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. (Q30823228) (← links)
- ANGSD: Analysis of Next Generation Sequencing Data. (Q30871440) (← links)
- The genomic landscape of mantle cell lymphoma is related to the epigenetically determined chromatin state of normal B cells (Q33585273) (← links)
- The impact of rare and low-frequency genetic variants in common disease (Q33613854) (← links)
- Inference of the Distribution of Selection Coefficients for New Nonsynonymous Mutations Using Large Samples (Q33642802) (← links)
- Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. (Q33840498) (← links)
- Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance (Q33883099) (← links)
- Genotype and SNP calling from next-generation sequencing data (Q33903792) (← links)
- A probabilistic method for the detection and genotyping of small indels from population-scale sequence data. (Q33926579) (← links)
- Estimation of allele frequency and association mapping using next-generation sequencing data (Q33929681) (← links)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Q34014340) (← links)
- Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome. (Q34055381) (← links)
- High-performance single-chip exon capture allows accurate whole exome sequencing using the Illumina Genome Analyzer (Q34061642) (← links)
- Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing (Q34066566) (← links)
- Demographic history and rare allele sharing among human populations (Q34197613) (← links)
- Learning about human population history from ancient and modern genomes. (Q34208814) (← links)