Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes.
about
The diploid genome sequence of an individual humanGenetic variation in an individual human exomeInsertion-deletion polymorphisms (indels) as genetic markers in natural populationsThe rhesus macaque is three times as diverse but more closely equivalent in damaging coding variation as compared to the humanLinkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genomePyroHMMvar: a sensitive and accurate method to call short indels and SNPs for Ion Torrent and 454 data.Performance evaluation of indel calling tools using real short-read dataUsing high-throughput sequencing transcriptome data for INDEL detection: challenges for cancer drug discovery.Differential gene flow of mitochondrial and nuclear DNA markers among chromosomal races of Australian morabine grasshoppers (Vandiemenella, viatica species group).Decoding of superimposed traces produced by direct sequencing of heterozygous indelsAssessing what is needed to resolve a molecular phylogeny: simulations and empirical data from emydid turtles.Insertion and deletion processes in recent human history.Microindel detection in short-read sequence data.Discovery and application of insertion-deletion (INDEL) polymorphisms for QTL mapping of early life-history traits in Atlantic salmonImpact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulation.MouseIndelDB: a database integrating genomic indel polymorphisms that distinguish mouse strains.Light whole genome sequence for SNP discovery across domestic cat breedsRate, molecular spectrum, and consequences of human mutationFast and SNP-tolerant detection of complex variants and splicing in short reads.LPA and PLG sequence variation and kringle IV-2 copy number in two populations.A probabilistic method for the detection and genotyping of small indels from population-scale sequence data.An initial map of insertion and deletion (INDEL) variation in the human genome.Genome-wide characterization of insertion and deletion variation in chicken using next generation sequencing.Small insertions and deletions (INDELs) in human genomesNatural genetic variation caused by small insertions and deletions in the human genomeIdentification of a truncated splice variant of IL-18 receptor alpha in the human and rat, with evidence of wider evolutionary conservationCharacteristics of de novo structural changes in the human genome.Simple sequence repeats in the national longitudinal study of adolescent health: an ethnically diverse resource for genetic analysis of health and behaviorExtreme genomic variation in a natural population.Correlated occurrence and bypass of frame-shifting insertion-deletions (InDels) to give functional proteins.Comparison and evaluation of two exome capture kits and sequencing platforms for variant callingSystematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB).Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms.The genomic landscape of short insertion and deletion polymorphisms in the chicken (Gallus gallus) Genome: a high frequency of deletions in tandem duplicates.Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome.Discovery and genotyping of structural variation from long-read haploid genome sequence data.BatAlign: an incremental method for accurate alignment of sequencing readsPExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPsAutomating sequence-based detection and genotyping of SNPs from diploid samples.Functional constraint and small insertions and deletions in the ENCODE regions of the human genome.
P2860
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P2860
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Comprehensive identification a ...... in 330 human candidate genes.
@en
Comprehensive identification a ...... in 330 human candidate genes.
@nl
type
label
Comprehensive identification a ...... in 330 human candidate genes.
@en
Comprehensive identification a ...... in 330 human candidate genes.
@nl
prefLabel
Comprehensive identification a ...... in 330 human candidate genes.
@en
Comprehensive identification a ...... in 330 human candidate genes.
@nl
P2093
P356
P1476
Comprehensive identification a ...... in 330 human candidate genes.
@en
P2093
Deborah A Nickerson
Mark J Rieder
Robert J Livingston
Tushar R Bhangale
P356
10.1093/HMG/DDI006
P577
2004-11-03T00:00:00Z