Natural genetic variation caused by small insertions and deletions in the human genome
about
Predicting the effects of frameshifting indelsHuman genetics and genomics a decade after the release of the draft sequence of the human genomeSequencing and analysis of a South Asian-Indian personal genomeUse of the Microbiome in the Practice of Epidemiology: A Primer on -Omic TechnologiesSInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence dataGenomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutationsLineage-specific genomics: Frequent birth and death in the human genome: The human genome contains many lineage-specific elements created by both sequence and functional turnoverEvolution of genomic structural variation and genomic architecture in the adaptive radiations of African cichlid fishesIdentification of indels in next-generation sequencing data.Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes.DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indelsAn international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.A practical method to detect SNVs and indels from whole genome and exome sequencing data.Reducing INDEL calling errors in whole genome and exome sequencing data.Comparison of insertion/deletion calling algorithms on human next-generation sequencing data.Performance evaluation of indel calling tools using real short-read dataSystematic analysis of microRNA targeting impacted by small insertions and deletions in human genome.A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i).Applications of the 1000 Genomes Project resourcesPan-cancer analysis reveals technical artifacts in TCGA germline variant callsThe association of insertions/deletions (INDELs) and variable number tandem repeats (VNTRs) with obesity and its related traits and complicationsmrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications.Health and population effects of rare gene knockouts in adult humans with related parentsGenome-wide characterization of insertion and deletion variation in chicken using next generation sequencing.An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs.Detection of structural variants and indels within exome data.Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.An integrative variant analysis suite for whole exome next-generation sequencing data.Straightforward inference of ancestry and admixture proportions through ancestry-informative insertion deletion multiplexing.Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencingRecombination drives vertebrate genome contraction.Fast and sensitive mapping of bisulfite-treated sequencing data.Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1SVM²: an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing dataGenome-wide patterns of standing genetic variation in a marine population of three-spined sticklebacks.Genomic variation and its impact on gene expression in Drosophila melanogaster.Insertion-deletions burden in copy number polymorphisms of the Tibetan populationCharacterisation and validation of insertions and deletions in 173 patient exomesSimple sequence repeats in the national longitudinal study of adolescent health: an ethnically diverse resource for genetic analysis of health and behaviorA comparison of 100 human genes using an alu element-based instability model
P2860
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P2860
Natural genetic variation caused by small insertions and deletions in the human genome
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Natural genetic variation caused by small insertions and deletions in the human genome
@ast
Natural genetic variation caused by small insertions and deletions in the human genome
@en
Natural genetic variation caused by small insertions and deletions in the human genome
@nl
type
label
Natural genetic variation caused by small insertions and deletions in the human genome
@ast
Natural genetic variation caused by small insertions and deletions in the human genome
@en
Natural genetic variation caused by small insertions and deletions in the human genome
@nl
prefLabel
Natural genetic variation caused by small insertions and deletions in the human genome
@ast
Natural genetic variation caused by small insertions and deletions in the human genome
@en
Natural genetic variation caused by small insertions and deletions in the human genome
@nl
P2093
P2860
P50
P356
P1433
P1476
Natural genetic variation caused by small insertions and deletions in the human genome
@en
P2093
Anup A Mahurkar
Caleb Webber
Daniel S Strassler
David M Kemeza
Scott E Devine
Todd H Creasy
Umar Farooq
W Stephen Pittard
P2860
P304
P356
10.1101/GR.115907.110
P577
2011-04-01T00:00:00Z