Pages that link to "Q34440676"

The following pages link to A likelihood-based framework for variant calling and de novo mutation detection in families (Q34440676):

Displaying 48 items.

• Using familial information for variant filtering in high-throughput sequencing studies (Q27008171) (← links)
• Genetic linkage analysis in the age of whole-genome sequencing (Q27027718) (← links)
• Genome-wide gene-environment interactions on quantitative traits using family data (Q30488613) (← links)
• Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data (Q30721849) (← links)
• Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing (Q30857788) (← links)
• FamSeq: a variant calling program for family-based sequencing data using graphics processing units (Q30865646) (← links)
• Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data (Q30965486) (← links)
• SeqMule: automated pipeline for analysis of human exome/genome sequencing data (Q30994226) (← links)
• Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data (Q31027821) (← links)
• A computational method for genotype calling in family-based sequencing data (Q31037146) (← links)
• MultiGeMS: detection of SNVs from multiple samples using model selection on high-throughput sequencing data. (Q31038281) (← links)
• A gradient-boosting approach for filtering de novo mutations in parent-offspring trios (Q33807679) (← links)
• A web-based interactive framework to assist in the prioritization of disease candidate genes in whole-exome sequencing studies (Q33860630) (← links)
• Reducing false-positive incidental findings with ensemble genotyping and logistic regression based variant filtering methods (Q33956672) (← links)
• Sequencing studies in human genetics: design and interpretation. (Q33981063) (← links)
• Sequencing depth and coverage: key considerations in genomic analyses (Q34398440) (← links)
• Comprehensive variation discovery in single human genomes (Q34572388) (← links)
• Joint genotype inference with germline and somatic mutations (Q34756290) (← links)
• Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection (Q34782823) (← links)
• A Bayesian framework for de novo mutation calling in parents-offspring trios (Q35541141) (← links)
• A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis (Q35541152) (← links)
• Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits (Q35669219) (← links)
• Comparison of genetic variants in matched samples using thesaurus annotation. (Q35834698) (← links)
• Genotype calling and haplotyping in parent-offspring trios (Q36489998) (← links)
• Rare variant detection using family-based sequencing analysis (Q36673312) (← links)
• Joint detection of copy number variations in parent-offspring trios (Q37002982) (← links)
• The impact of genotype calling errors on family-based studies (Q37027403) (← links)
• The Qatar genome: a population-specific tool for precision medicine in the Middle East (Q37053589) (← links)
• Identifying rare variants associated with complex traits via sequencing (Q37316697) (← links)
• Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees (Q37342111) (← links)
• Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster. (Q37550264) (← links)
• The next-generation sequencing revolution and its impact on genomics (Q37672566) (← links)
• Advances in biotechnology and informatics to link variation in the genome to phenotypes in plants and animals (Q38089627) (← links)
• Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing (Q38229549) (← links)
• Eye color: A potential indicator of alcohol dependence risk in European Americans (Q38386678) (← links)
• Systematic review of next-generation sequencing simulators: computational tools, features and perspectives (Q38805939) (← links)
• DeNovoGear: de novo indel and point mutation discovery and phasing. (Q39031240) (← links)
• mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing (Q41571023) (← links)
• Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing. (Q47445785) (← links)
• Precise detection of de novo single nucleotide variants in human genomes. (Q53824685) (← links)
• HAPDeNovo: a haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data. (Q55387186) (← links)
• Measuring coverage and accuracy of whole-exome sequencing in clinical context (Q57646393) (← links)
• Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy (Q58787065) (← links)
• Comparative Analysis for the Performance of Variant Calling Pipelines on Detecting the Mutations in Humans (Q64039275) (← links)
• Mendelian Inconsistent Signatures from 1314 Ancestrally Diverse Family Trios Distinguish Biological Variation from Sequencing Error (Q64282939) (← links)
• Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates (Q89865831) (← links)
• The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition (Q91132911) (← links)
• DENDRO: genetic heterogeneity profiling and subclone detection by single-cell RNA sequencing (Q92640167) (← links)