dbSNP cohort

Aliases

Database of Single Nucleotide Polymorphisms, dbSNP database, dbSNP132

Related entities (8)

Mentioned in (35)

Papers in which this entity is mentioned.

• KILDA: identifying KIV-2 repeats from kmers. (2025)
• Osteosarcoma PDX-Derived Cell Line Models for Preclinical Drug Evaluation Demonstrate Metastasis Inhibition by Dinaciclib through a Genome-Targeted Approach. (2024)
• Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
• Best practices for variant calling in clinical sequencing. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
• PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites. (2018)
• SvABA: genome-wide detection of structural variants and indels by local assembly. (2018)
• Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. (2017)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• GeneiASE: Detection of condition-dependent and static allele-specific expression from RNA-seq data without haplotype information. (2016)
• The IPD and IMGT/HLA database: allele variant databases. (2015)
• Genetic linkage analysis in the age of whole-genome sequencing. (2015)
• VariantDB: a flexible annotation and filtering portal for next generation sequencing data. (2014)
• DNA methylation signatures link prenatal famine exposure to growth and metabolism. (2014)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. (2013)
• A comparative analysis of algorithms for somatic SNV detection in cancer. (2013)
• Landscape of transcription in human cells. (2012)
• A cross-sample statistical model for SNP detection in short-read sequencing data. (2012)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Integrative analysis of the melanoma transcriptome. (2010)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
• SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (2009)
• Marker selection for genetic case-control association studies. (2009)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
• Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
• A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)
• SNPs3D: candidate gene and SNP selection for association studies. (2006)

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