Pages that link to "Q30912274"

The following pages link to Mapping Bias Overestimates Reference Allele Frequencies at the HLA Genes in the 1000 Genomes Project Phase I Data (Q30912274):

Displayed 40 items.

• Parallel or convergent evolution in human population genomic data revealed by genotype networks (Q31119186) ‎ (← links)
• The wolf reference genome sequence (Canis lupus lupus) and its implications for Canis spp. population genomics (Q32175916) ‎ (← links)
• Genome graphs and the evolution of genome inference (Q33622582) ‎ (← links)
• A novel RNAseq-assisted method for MHC class I genotyping in a non-model species applied to a lethal vaccination-induced alloimmune disease (Q36020341) ‎ (← links)
• Phylogenomic Insights into Mouse Evolution Using a Pseudoreference Approach (Q36321850) ‎ (← links)
• Evaluation of MC1R high-throughput nucleotide sequencing data generated by the 1000 Genomes Project (Q36367163) ‎ (← links)
• Variation in Linked Selection and Recombination Drive Genomic Divergence during Allopatric Speciation of European and American Aspens (Q37025072) ‎ (← links)
• Common coding variants in the HLA-DQB1 region confer susceptibility to age-related macular degeneration (Q37351470) ‎ (← links)
• A genomic perspective on HLA evolution (Q38688783) ‎ (← links)
• Biomechanisms of Comorbidity: Reviewing Integrative Analyses of Multi-omics Datasets and Electronic Health Records (Q38796894) ‎ (← links)
• Comparative analysis of de novo assemblers for variation discovery in personal genomes (Q38838300) ‎ (← links)
• kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity (Q41702237) ‎ (← links)
• What has GWAS done for HLA and disease associations? (Q47816520) ‎ (← links)
• HLA and proteasome expression body map. (Q52340092) ‎ (← links)
• Long reads: their purpose and place (Q57737681) ‎ (← links)
• iMapSplice: Alleviating reference bias through personalized RNA-seq alignment (Q58791356) ‎ (← links)
• AltHapAlignR: improved accuracy of RNA-seq analyses through the use of alternative haplotypes (Q59223463) ‎ (← links)
• FORGe: prioritizing variants for graph genomes (Q60044442) ‎ (← links)
• Impact of index hopping and bias towards the reference allele on accuracy of genotype calls from low-coverage sequencing (Q60044970) ‎ (← links)
• The Effect of Balancing Selection on Population Differentiation: A Study with HLA Genes (Q60575223) ‎ (← links)
• Characterizing the Major Structural Variant Alleles of the Human Genome (Q63359159) ‎ (← links)
• Accurate sequence variant genotyping in cattle using variation-aware genome graphs (Q64054486) ‎ (← links)
• Expression estimation and eQTL mapping for HLA genes with a personalized pipeline (Q64099439) ‎ (← links)
• HLA-H: Transcriptional Activity and HLA-E Mobilization (Q89495007) ‎ (← links)
• Sources of bias in genomics research of oral and dental traits (Q89590552) ‎ (← links)
• Tumor suppressor genes and allele-specific expression: mechanisms and significance (Q89736899) ‎ (← links)
• Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project (Q89777824) ‎ (← links)
• Valid Post-clustering Differential Analysis for Single-Cell RNA-Seq (Q90108766) ‎ (← links)
• CHOP: haplotype-aware path indexing in population graphs (Q90242486) ‎ (← links)
• ReQTL: identifying correlations between expressed SNVs and gene expression using RNA-sequencing data (Q90557541) ‎ (← links)
• Fast and accurate genomic analyses using genome graphs (Q91045766) ‎ (← links)
• Accuracy of whole-genome sequence imputation using hybrid peeling in large pedigreed livestock populations (Q91576403) ‎ (← links)
• Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder (Q91644471) ‎ (← links)
• Developing a High-Quality Linkage Map for the Atlantic Killifish Fundulus heteroclitus (Q91751965) ‎ (← links)
• SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes (Q92025187) ‎ (← links)
• Paragraph: a graph-based structural variant genotyper for short-read sequence data (Q92128944) ‎ (← links)
• The presence and impact of reference bias on population genomic studies of prehistoric human populations (Q92203803) ‎ (← links)
• Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data (Q92501401) ‎ (← links)
• A customized scaffolds approach for the detection and phasing of complex variants by next-generation sequencing (Q99418198) ‎ (← links)
• High-Throughput Sequencing to Investigate Associations Between HLA Genes and Metamizole-Induced Agranulocytosis (Q99711638) ‎ (← links)