Pages that link to "Q35958578"
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The following pages link to Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome (Q35958578):
Displaying 50 items.
- Incredible RNA: Dual Functions of Coding and Noncoding (Q26748037) (← links)
- Human Knockout Carriers: Dead, Diseased, Healthy, or Improved? (Q26764736) (← links)
- Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders (Q26783154) (← links)
- Report on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada. (Q30355125) (← links)
- A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family (Q30385875) (← links)
- regSNPs-splicing: a tool for prioritizing synonymous single-nucleotide substitution (Q30400919) (← links)
- Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation. (Q31132461) (← links)
- Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences (Q31144431) (← links)
- Allelic imbalance of somatic mutations in cancer genomes and transcriptomes. (Q33687737) (← links)
- Non-Coding Loss-of-Function Variation in Human Genomes (Q33878483) (← links)
- Health and population effects of rare gene knockouts in adult humans with related parents (Q34046351) (← links)
- Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans (Q34475541) (← links)
- Translating RNA sequencing into clinical diagnostics: opportunities and challenges. (Q34519034) (← links)
- Tools and best practices for data processing in allelic expression analysis (Q35779348) (← links)
- The landscape of genomic imprinting across diverse adult human tissues (Q35793503) (← links)
- The Characteristics of Heterozygous Protein Truncating Variants in the Human Genome (Q35862547) (← links)
- A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans (Q35907724) (← links)
- Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease (Q35991193) (← links)
- SNPsplit: Allele-specific splitting of alignments between genomes with known SNP genotypes. (Q36080499) (← links)
- Functional genomics bridges the gap between quantitative genetics and molecular biology (Q36084283) (← links)
- Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity (Q36233059) (← links)
- The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies (Q36324942) (← links)
- A Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project (Q36362149) (← links)
- Systematic identification of genes with a cancer-testis expression pattern in 19 cancer types (Q36534662) (← links)
- Pseudo-Reference-Based Assembly of Vertebrate Transcriptomes (Q36731839) (← links)
- Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error (Q36764466) (← links)
- Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized Medicine (Q36840024) (← links)
- A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis (Q37166229) (← links)
- Identification of Siglec-1 null individuals infected with HIV-1. (Q37181228) (← links)
- Proteogenomics: Integrating Next-Generation Sequencing and Mass Spectrometry to Characterize Human Proteomic Variation (Q37190570) (← links)
- Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing (Q37248390) (← links)
- Rare variant phasing and haplotypic expression from RNA sequencing with phASER (Q37260317) (← links)
- Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients (Q37296773) (← links)
- Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population (Q37461564) (← links)
- Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders. (Q38429616) (← links)
- Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians. (Q38611133) (← links)
- Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance. (Q38656663) (← links)
- Evolution by gene loss. (Q38810622) (← links)
- Discovery of rare variants for complex phenotypes. (Q38843404) (← links)
- The roles of RNA processing in translating genotype to phenotype (Q39009636) (← links)
- The rules and impact of nonsense-mediated mRNA decay in human cancers (Q39400851) (← links)
- Integrating RNA sequencing into neuro-oncology practice. (Q39459649) (← links)
- RNA expression in human retina (Q40064842) (← links)
- Human Retrotransposon Insertion Polymorphisms Are Associated with Health and Disease via Gene Regulatory Phenotypes (Q41203183) (← links)
- Insights into beta cell regeneration for diabetes via integration of molecular landscapes in human insulinomas. (Q42282703) (← links)
- Improving genetic diagnosis in Mendelian disease with transcriptome sequencing (Q42343467) (← links)
- Landscape of X chromosome inactivation across human tissues (Q42696435) (← links)
- Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change. (Q43794949) (← links)
- A Comparison of mRNA Sequencing with Random Primed and 3'-Directed Libraries. (Q45920297) (← links)
- Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits. (Q46000774) (← links)